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"Small Room". The tiny but extremely complicated units out of which all lifeforms are made out of. They are alive, and they all die. They can replicate independently. They harvest and use energy. They are the smallest living things. Its parts will deteriorate if separated from the rest of it, however they may be removed whole from an organism and thrive in vitro. Their internal part placement, nature, and interactions are strictly regulated, controled, and excercised. All its parts are constantly being broken down and replaced. It can respond very quickly to changing environmental conditions. They produce many different chemicals that would nearly never form spontaneously. |
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An instrument used to look at very small objects such as cells, viruses, molecules, and even atoms.
It makes use of an optical lens to magnify the image of the small object.
They were first invented in the 1600s. |
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An instrument used to look at very distant objects such as planets, stars, and other objects in space.
It makes use of the optical lens to change the magnification of the object, which would otherwise appear extremely tiny. |
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A specifically shaped piece of glass found in microscopes and telescopes.
They were invented very long ago and were first used in corrective eye glasses. |
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The person who discovered cells. Belonged to the Royal Society of London. Wrote Micrographia.
He cut a piece of cork with a sharp razor and viewed it under a microscope. He saw a structure similar to a honeycomb. He named the pores he saw "cells" after the rooms of monks in a monastery. We know now that what he was seeing was the dead cell walls of the cork tree.
He was the one who confirmed Anton van Leeuwenhoek's discovery of protists and bacteria. |
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The person who discovered protists and bacteria. Persued science for the curiosity, not the glory.
A clothes and button salesman who spent his spare time making optical lenses and microscopes. Was in correspondence with the Royal Society of London.
He examined a drop of pond water with a microscope and saw moving objects which he named "animalcules". We know now that what he saw were protists or bacteria. He also found bacteria in scrapings from his teeth.
His findings were met with skepticism until Robert Hooke confirmed his discoveries. |
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One of the people who helped develope cell theory.
A lawyer and botanist. He was a colleague of Theodor Schwann. In the 1830s he made the discovery that all plants were made from cells and that plant embryos consisted of a single cell.
He made the incorrect assumption that a cell could arise spontaneously from non-cellular material. This notion remained unquestioned for a number of years. |
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One of the people who helped develop cell theory.
A zoologist. He was a colleague of Matthias Schleiden. He made the discovery that all organisms, including animals and humans, were composed of cell(s), and that the cell was the structural unit of life.
He made the incorrect assumption that a cell could arise spontaneously from non-cellular material. This notion remained unquestioned for a number of years. |
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The person who debunked the idea of Matthias Schleiden and Theodor Schwann that cells can arise spontaneously from non-cellular material.
A pathologist. |
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A set of laws of life
1. All organisms are composed of one or more cells.
2. The cell is the structural unit of all life
3. Cells can only arise by division from pre-existing cells. |
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All living things are made out of one or more cells. This is why viruses are not considered alive. All living things die. All cells die. Death is a property of life. |
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A property of life. All living things die. All cells die.
Sometimes cells will "commit suicide" due to internal programing or signals from outside. This way an organism can trim off unneeded or dangerous (such as cancerous) cells. |
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A married couple from Hopkins University.
In 1951 they cultured in vitro the tumor cells of Henrietta Lacks and called them "HeLa" cells, after the donor. They discovered that unlike normal tissues, cancerous tissues can be cultured indefinitely in vitro. |
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To culture something in a petri dish in a lab.
Cells are much more easily studied this way. This is an essential tool of the cellular biologist.
When a patient gets a bacterial infection one of the first steps of diagnosis is to culture it to see what bacteria it is. We can only record and "discover" bacteria that we can culture, so many species, such as those in the ocean, are left undiscovered. |
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Levels of Complexity in Life |
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Living things are arranged in many compound layers of complexity from atoms to organisms. Each layer has a very specifically regulated way its components are arranged. Even small mistakes (at any point) can have life altering effects on the higher levels. At the lower levels there is not much difference between species; for example both humans and trees have the organelles mitochondria.
1. Atoms are arranged into small molecules.
2. Small molecules are arranged into larger polymers.
3. Polymers are arranged into complexes.
4. Polymer complexes are arranged into subcellular organelles.
5. Organelles are arranged into cells.
6. Cells are arranged into organisms. |
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Small protrusions from a cell to increase surface area. Epithelial cells have them to increase nutrient uptake. Each one has an internal skeleton made from actin protein. |
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An organelle that provides usable energy in the form of ATP to the rest of the cell, fueling cell functions. It measures 2 μm in diameter and can be a variety of shapes, even tubular. They reproduce by fission, and can fuse with other mitochondria.
There are two membranes, the OMM and IMM. Its membrane is produced separately from the rest of the cell. Sometimes it sends vesicles to the peroxisomes. When ADP levels drop, it stops producing ATP. |
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The "blueprints" of an organism. One of the polymers that set life apart from non-living things. The monomers are nucleotides. It is an anti-parallel, right-handed double helix strand 2 nm in diameter composed of the bases guanine, adenine, thymine, and cytosine. The strands are held together by hydrogen bonds. Each strand has a 5' end and a 3' end. More stable than RNA.
Information is stored in its sequences for cell structure, cell activity, and cell reproduction. Proteins are the "workers" who follow the "blueprints". Not all the mechanisms by which cells use and transmit these genes are discovered yet.
Packaged in a set of chromosomes inside the nucleus.
Humans have enough sequences to fill a million pages of text. |
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Cells reproduce by division into two smaller cells. The contents of the "mother" cell are distributed to the two "daughter" cells evenly. Prior to the split, all genetic material is duplicated and each "daughter" recieves an equal share of the genes.
Usually both cells are equal in volume, but there are exceptions, such as in mammalian oocyte division. |
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Required by all biological processes.
Nearly all lifefroms ultimately get it from the sun. The sun emits it in the form of electromagnetic radiation, which is absorbed by light-absorbing pigments inside photosynthetic cells. Organisms that do not have photosynthetic cells then take it from the organisms that do by eating or absorbing their cells or cell remains. |
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The process by which photosynthetic cells convert energy from the sun's electromagnetic radiation into chemical energy in the form of carbohydrates. Requires carbon dioxide and water, releases oxygen. The opposite of aerobic respiration. |
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A sugar that is the most common molecular source of energy in humans. The building block of starch and glycogen. It is metered out by the liver into the blood. Inside the cell it is taken apart and converted by the mitochondrion into ATP by glycolysis and the TCA cycle. This releases 686 kcal of energy for every molecule of glucose. |
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A short-term energy storage molecule synthesized by the mitochondria. It is the "currency" of the cell and powers all cell functions, such as breaking down and rebuilding macromolecules and organelles. After it is used up it turns into ADP and must be reconverted into ATP by the mitochondria. |
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The sum of an organisms chemical reactions.
Cells must break down and creat chemicals in reactions that would almost never occur spontaneously. They do this with enzymes.
Each step of all processes in a cell must occur chemically spontaneously in a way that triggers the next step of the process. The steps were developed over eons of evolutionary trial and error. |
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A protein used by a cell to lower the activation energy of a chemical reaction, thus greatly increasing the probability that it will occur. Cells use them to create many chemicals that would almost never occur spontaneously. |
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A property of life. Materials are transported in, out, and around a cell, they are assembled or disassembled, and even entire cells can relocate themselves.
It is done with motor proteins. |
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A protein that creates all mechanical motion inside a cell or in moving an entire cell.
Push or pull vesicle cargo along the cytoskeleton. Have two "feet" and do a walking motion along the microtubule or microfilament. |
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All cells can respond to it from receptors in their cell wall. Forms may include hormones, growth factors, extracellular materials, temperature, pH, light, or structures on surrounding cells. Its effects are diverse and may include metabolism changes or even self-induced death. |
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The mechanism by which cells are able to protect themselves from dangerous fluctuations in composition. It keeps the cell at homeostasis, even through any changes in cells, such as changes brougt on by external stimuli.
If it is damaged, it can be very bad for a cell, and it can be mutated, become cancerous, and/or die. |
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An embryologist famous for his experiments with sea urchin embryos.
He discovered that if he separated the first two cels of a sea urchin embryo the two cells would form into two separate but genetically identical sea urchins.
This raises some important questions, such as how does the separated cell know to develop into a full sea urchin, and not half a sea urchin? How does the cell know that its "sister" cell is not there? How does this knowledge alter the way the cell grows?
We still do not fully know the answers. |
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A polymer that forms very specific shapes, often in larger complexes. One of the polymers that sets life apart from non-living things. It has an amino (N)-terminus and a carboxy (C)-terminus.
They are formed from mRNA sequences and ribosomes. and have a myriad of functions in the cell.
They have a lifespan between a few seconds and a few weeks. They are destroyed by proteasomes. |
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Last Universal Common Ancestor (LUCA) |
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Definition
The theoretical first cell ever. It lived almost 4 billion years ago, relatively recently after the Earth's crust solidified. It is the ancestor of all life on Earth. No one knows where it came from. It is likely that it evolved from a form of pre-cellular life which itself evolved from non-living organic material in the primordial seas. |
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The mechanism by which organisms develop into different more "advanced" organisms. There is genetic variation between individuals, this is what causes natural selection.
It has been occuring for almost 4 billion years, since LUCA, and is still an ongoing occurance. |
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"Before nucleus". The "simpler" of the two types of cells. This kingdom has two domains: Archaea and Bacteria. They are older than eukaryotes. The first definite sign of them (in fossils) is over 2.7 billion years old, but they may be as old as almost 4 billion years. They are very succesful. In terms of numbers they are far more sucessful than eukaryotes. They are better at encorporating foreing DNA and adapting to environments.
There are trillions of them living just on or in you alone; they live in your intestines, making essential vitamins and fighting off pathogens. The species representation of this bacteria may change with different factors such as physical health and diet.
They are 5 to 10 μm in diameter. Because of their morphology they are difficult to see with a microscope and difficult to distinguish between. 6000 species are discovered, but this is an estimated 0.01% of the true number of species.
Their genetic material is kept in a nucleoid. They have less DNA than eukaryotes; they have only one chromosome with a circular DNA strand.
They are small enough that they need no intracellular transport system; diffusion of material is enough to keep the center of the cell nurished. |
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"True nucleus". The "more advanced" of the two types of cells. This category includes protists, fungi, plants, and animals.
They are younger than prokaryotes, but it is unclear when they first arose, but they are older than 600 million years.
Their nuclei are separated from their cytoplasm by the nuclear envelope. Their DNA is packaged in multiple chromosomes, each containing a linear DNA strand. They have complex, membrane-bound organelles. They have specialized organelles for aerobic respiration and (sometimes) photosynthesis: mitochondria and chloroplasts. They have cytoskeletal systems and an intracellular transport system. They may have flagella and cilia. They may undergo phagocytosis. They may have cellulose-containing cell walls. They form spindles during cell division. There are two copies of genes per cell, one from each parent. They have three different RNA synthesizing enzymes. They may have sexual reproduction with meiosis and fertilization. |
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An type of bacteria that over 2.7 billion years old, that is still thriving today. They excrete O2 as a biproduct of photosynthesis; they were responsible for the rise in O2 levels in the atmosphere on Earth 2.4 billion years ago. They are the exception to the rule that prokaryotes don't have membrane-bound organelles: they have photosynthetic membranes. Unlike plants they can fix atmospheric nitrogen (N2) into ammonia (NH3). To survive and thrive they only need N2, CO2, water, and light. |
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Eukaryotic organisms that appeared only 600 million years ago. For the first 3 billion years after LUCA, all life on Earth was single-celled. |
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A membrane-bound organellein eukaryotes. It measures 5 to 10 μm in diameter. Can be up to 10% of the cell volume. It is not always round or in the center of the cell. It stores, replicates, repairs, and expresses genetic material. It synthesizes ribosomes. It is surrounded by the nuclear envelope. It contains chromatin, nucleoplasm, nuclear matric, and the nucleolus. |
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Endoplasmic Reticulum (ER) |
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Definition
An organelle that manufactures lipids and proteins. It is a dynamic system of interconnected membranes forming cisternae, tubules, and vesicles encloing a lumen. It is near the nucleus and has two regions: peri-nuclear and cortical. It is has two types which are continuous with each other: rough and smooth. Both types perform lipid and cholesterol synthesis. The function, structure, and size varies between species and cell type. Found only in eukaryotes. |
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An organelle that sorts, modifies, and transports substancea from the ER. Discovered by Camillo Golgi, who gave it his name. It was suspected to be an artifact until freeze-fracturing showed that it was not.
It produces complex polysaccharides. Series of less than 8 flattened stacked membranous cisternae. 0.5 to 10 μm in diameter. It has cis, medial, and trans regions. They are supported by protein scaffolfing (spectrin, ankyrin, and actin) and there are other proteins which aid in replication during mitosis. Each cisternae is chemically unique. There are two theories on how it forms: the cisternal maturation model and the veisicular transport model. |
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An organell that is the site of photosynthesis and the synthesis of cabohydrates, amino acids, fatty acids, and terpenoid compounds. Only plants have chloroplasts. It is bound by a double, but produces its membrane separately from the rest of the cell. It has thylakoids in the stroma. It is motile within the cell. It has its own circular DNA. |
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The large, central organelle in a plant cell.Its membrane is calld the tonoplast. It may take up to 90% of the cell's volume. It performs many essential functions. It contains ions, sugars, proteins, toxins, and many other substances. Used for storage and mechanical support. Proteins are produced in the RER.
It may contain toxins as a defense mechanism against herbivores or parasites when the plant is injured.
Plant's down have the same excretory system as in animals, by-products of processes may be dumped in the vacuole.
It acts as the cell's lysosomes, and it has hydrolytic enzymes in it and a low pH maintained by V-type H+-ATPase. |
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An organelle without a membrane. They may be in the cytoplasm or bound to the RER. It translates proteins from mRNA. In prokaryotes they are much smaller than in eukaryotes. It is made from 3 to 5 RNA strands and 50 to 90 proteins. |
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A structure that forms during the division of a eukaryotic cell. It ensures that both daughter cells recieve an equal share of the genes. Prokaryotic cells lack this. |
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When a prokaryotic cell forms an F pilus tube that connects to a neighboring bacterium. It passes some genetic material to the other bacterium. The acceptor cell may accept some of the DNA from the donor. |
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A structure that protrudes from some cells. It is attached to motor proteins and is used to propel a cell through its medium. Some bacteria can rotate theirs 1000 times per second.
The mechanisms of motion are different in prokaryotes than in eukaryotes. |
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A colony of bacteria. Different cells perform different functions, however it is not considered a multicellular organism. An example would be the film found on human teeth. |
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A domain of the prokaryotes. They are more related to eukaryotes than bacteria.
They can live in very inhospitable environments. They are sometimes called the "extremophiles".
They include methanogens (methane producers), halogens (live in highly salty waters), acidophile (live in very low pH), and thermophiles (live at very high temperatures). Many of these species may also be found in normal conditions. |
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A domain of prokaryotes. They can live in every conceivable habitat on Earth, even deep beneath the bedrock. Some species divide only once every hundred years!
They have 2500 to 3500 genes, usually on a single DNA molecule. |
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They smallest living organism. They are a type of bacteria with no cell wall and less than 500 genes. |
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The process by which cells in a muticellular orgnism are specialized. It occurs in embryos.
They used to think that cells would discard unneeded genes. This was disproved by clones such as Dolly the Lamb.
Each cell has a subset of genes which indicates what genes to activate and what to not activate. Cells in different regions of the embryo take on different sizes, shapes, and chemical compositions. They have different representation and location of organelles. They eventually take on different tasks in the organism. |
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A model organism. It is a prokaryote found in the human digestive tract.
Using synthetic biology, one company was succesful in incorporating the DNA of 3 other bacterial species to make it produce biofuel ethanol |
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Saccharomyces cerevisiae. A model organism. It is budding yeast used in baking bread. A unicellular fungus. It is the least complex eukaryotic model organism. It has many proteins common to humans. It has a small genome. It can survive aerobic as well as anaerobic condition. It can be cultured as a haploid, making it ideal for mutant analysis. It can reproduce both sexually and asexually, sometimes forming long filaments by budding from the mother cell. The haploids spores are called ascospores, stored in the ascus. It has two breeding types, a and α, which fuse to make a diploid cell. |
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Arabidopsis thaliana. A model organism. A flowering plant. It has a small genome. It has a large seed production and reproduces rapidly. It takes 5 weeks to reach maturity. It does not grow to be very large. It is related to radishes, cabbage, and canola, but has no agricultural value. |
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A model organism. A nematode. It has a defined number of cells. It is easily cultured. It can be frozen and survive. It has a short generation time. |
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A model organism. A fruit fly. It has a short lifespan. |
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Mus musculus. A model organism. Their lifespan is around 2 years, reaching sexual maturity at 7 to 8 weeks. Important in biomedical research. Popular test subjects for drugs, chemicals, and foods. They are more closely related to humans than any of the other model organisms. They reproduce sexually. |
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Organisms commonly used for scientific research. They must have characteristics that make them easy or useful to study, such as a short generation period, small size, genetic variation and protein similarities to humans. Over many years, large colonies are kept for various research projects. Collections of mutant strains may be kept. |
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A measurement equal to 10-6 meters. These are the units that cells and organelles are measured in. |
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A measurement equal to 10-9 meters. These are the units that molecules are measured in. |
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A measurement equal to 10-10 meters. This is the diameter of a hydrogen atom. |
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A region of a prokaryotic cell where the genetic material is stored. There are no true boundaries. |
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Why cells cannot be larger in size |
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Definition
1. Only one set of chromosomes, constantly bing copied. Only so much mRNA can be produced at a time, limiting cell size.
2. As volume increases surface area to volume ratio shrinks, putting strain on the import/export system of the cell. To circumvent this some cells are very long or have microvillli.
3. Oxygen must diffuse to the center of the cell. Too large a cell will experience oxygen deprivation at its core. |
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The quest to create a living cell from non-living materials. This has no practical application, it is simply awesome. It would give insight on how LUCA came to be. Scientists are nowhere near accomplishing it. Some people say it would be unethical.
Another branch of this is genetically creating new species out of existing ones for medicine, industry, or the environment. |
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The group who in 2007 first changed the species of a bacteria. They introduced new DNA to a host and the host changed its characteristics and became a different species.
These methods are now used to create organisms that can produce pharmaceuticals, fuels, or other useful chemicals. |
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Term
Tobacco Mosaic Virus (TMV) |
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Definition
A virus that infects tobacco plants. Contains RNA. It was the first virus ever discovered. It was proved not to be a bacteria, as initially thought, due to its small size. |
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The person who discovered viruses. In 1892 he forced the sap of a tobacco plant infected with tobacco mosaic disease through a filter with holes small enough to capture any bacteria. The filter was uneffective at sanitizing the sap. He determined that some diseases are caused by pathogens smaller than bacteria. He called them viruses. |
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The person who discovered that viruses are not cellular. From the Rockefeller Institute.
In 1935 he crystalized tobacco mosaic disease. This proved that the virus was a well defined shape with an uncomplicated structure, definately not cells.
He incorrectly concluded that viruses were proteins. |
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The cause of many diseases across all lifeforms. For humans they include HIV, polio, influenza, cold sores, measels, and they can cause some cancers.
They come in a great variety of shapes, sizes, and structures. They cannot reproduce without a living host; each one has a specific range of hosts it can attack. They have no metabolic processes. They are not considered living.
It exists outside of cells as a free particle called a virion.
They are a proetin coat surrounding genes inside a capsid. The 3 to 4 genes may be DNA or RNA.
They may be used to conduct scientific research on gene replication and expression. They are used to introduce foreign genes to complex cells. They can be used to treat human diseases. Viruses that effect pests may be used as a form of pest control. |
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The free-moving particles that are viruses while outside of a cell. |
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The protein coat surrounding the genes of a virus. It is formed from a number of proteins. The fewer proteins, the less genes are required for the virus.
Some are polyhedron shaped with planar faces, such as a 20-sided icosahedron.
Some have phospholipids encorporated into them, stolen from their parent host as they exited the cell.
They have proteins on their surface that bind to particular surface components of the host cell and facilitate the virus's entry to the cell. How specific this protein is determines the virus's host range. |
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Viruses that attack bacteria. In terms of numbers they are the most abundant biological entity on Earth.
They are the most complicated viruses. They have a polyhedral head containing DNA, a cylindrical neck, and tail fibres. It resemples the moon landing pod.
They may be used to treat bacterial infections as an alternative to antibiotics. They may be used to keep food from bacterial contamination. |
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A virus that is related to AIDS. It is sexually transmitted or transmitted through the blood. It has the glycoprotein gp 120 on its capsid, enabling it to attack white blood cells. As it exits the cell, it takes with it some phospholipids. |
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A virus with a wide range of mammalian hosts, including dogs, bats, and humans. |
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A virus that in 1918 killed 30 million people, especially young adults.
Scientists have been able to recreate the influenza artifically by analysing the preserved tissues of a Native American woman who died of the influenza in 1918 and was buried in permafrost that preserved her body.
The reconstructed virus killed 100% of a population of mice. Only mice who had been vaccinated could survive.
By analyzing the genes, they determined that the disease was passed to humans from birds, probably chickens. |
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A type of viral infection where the virus ceases the normal synthetic activities of the cell and redirects the host to create nucleic acids and proteins that assemble into virions. The cell then ruptures (lyses) and releases the virions. |
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A type of viral infection where the virus does not kill the host cell. Instead it inserts its DNA into the hosts's chromosomes. It can have several effects.
1. The cell behaves normally until exposed to external stimuli that activate dormant viral DNA, leading to lyses.
2. The cell produces virions that bud the cell surface but do not break it. Eample: HIV. The cell remains alive as a virus factory.
3. The host loses control of its growth and division rate and becomes a malignant tumour. |
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The person who discovered viroids. From the USDA. In 1971 he found that potato spindle tuber disease was caused by naked strand of RNA laking a protein capsid. Named it a "viroid". |
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A virus lacking a capsid. It is a naked strand of RNA from 240 to 600 nucleotides, one tenth the size of the smallest viruses.
All biochemical activities are completed by the host cell. It makes use of polymerase II, the enzyme normally used for making mRNA.
It kills its host by messing up their normal gene expression path.
Examples: cadang-cadang in coconuts, potato spindle-tuber disease, and a disease that effects chrysanthemums. |
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A book written by Robert Hooke on his findings of cells. |
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The study of cells. It has taken us 400 years to get to the level of knowledge we have on cells today. We still don't know everything.
50 years ago DNA was discovered, and in the 90s many genomes of organisms were recorded, but this still does not tell us everything.
In a diagram the cell has neatly placed, still organelles. In reality everything is cluttered and moving! Nothing is written in stone. |
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A membrane-bound organelle 0.1 to 1.0 μm in diameter. Their job is detoxification. In plant seedlings they are called glyoxysomes. All eukaryotic cells have them. Proteins being imported carry a PTS and import mainly posttranslationally. It is the only organelle that can import fully folded proteins, how is unknown. In plants they move along the protein actin. In animals they move along microtubules. They reproduce by splitting, or from the ER. They are pleomorphic and can form peroxules. They are densely filled with cyrstalline oxidative enzymes. There are over 50 types of enzymes, including catalase. They oxidize VLCFAs and synthesize plasmalogens. They produce and then quickly break down hydrogen peroxide. |
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A type of organelle found in eukaryotes. Sometimes they undergo activities similar to prokaryotes, such as conjugation. They are pleomorphic. The "pilus" formed during plastid conjugation is called a stromule. This leads us to belive they may have evolved from prokaryotes phagosized into a eukaryote. They are surrounded by a loose ER cage. Include mitochondria, chloroplasts, etioplsts, chromopalsts, leukoplasts, amyloplasts, elaioplasts, proteinoplasts, and statoliths. |
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A cell in a multicellular organism that can differentiate into any cell type of that organism. |
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A complex of DNA, RNA, and proteins (mainly histones). Found only in eukaryotic cells, in their chromosomes. It protects the DNA and has crucial roles in cell division and gene expression. |
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Equal to the product of the powers of each lens involved in magnification. |
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The fluid inside a cell. It is divided into compartments (organelles) by membranes in eukryotes. It is a very crowded and complex place. It is separate from the endomembrane lumen. |
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A microscope consisting of an ocular lens, objective lens, specimen, condenser lens, and a light source. Light shines through the specimen. You can't see opaque objects because they will appear as dark blots. Translucent objects are also hard to see because they resemble the background. Resolution is dependent on the wavelength of the light. |
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The lens in a light microscope that focuses the light from the light source onto the specimen. |
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The lens in a light microscope that takes in the light that is shining through the specimen. It forms an enlargd real image of the specimen and shines it on the ocular lens.
When you adjust the focusing knob, you change the distace between this lens and the specimen; this means you can only look at one level of focus. The other levels may make the image look blurry. |
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Definition
The second lens in a light microscope which takes the real image from the objective lens and elargens it some more and makes it into a virtual image. It then goes into your eye, giving you an enlarged image of the specimen. |
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Definition
The object that we are looking at using a microscope. |
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Definition
The amount of detail in an image. How clear an image looks. Determined by the distance between the closest two airy disks which can be distinguished. |
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Definition
When you magnify something, but the resolution stays the same. This may happen if you increase the power of the ocular lens but not the objective lens in a light microscope; the objective lens has no more information to provide the ocular lens with. |
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Definition
A phenomenon where light coming from two very close points appear like the same point. This depends on the wavelength of the light. A microscope's resolving power is based on this. |
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Definition
A measure of the ability of a microscope defined by the minimum distance between two points where they can still be defined as separate points.
d = (0.61λ) / (n * sin α)
d = resolving power
λ = wavelength of light
n = refractive index of the medium present between the specimen and the objective lens
α = half the angle of the cone of light entering the objective lens. Related to numerical aperture. |
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Term
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Definition
A measure of the light-gathering ablities of a lens. Defined by the denominator of the equation for resolving power. The number will be on the side of the lens.
n * sin α
In air the highest possible value is 1. The sine of 90º is 1, and the refractive index of air is 1.
You can get higher NA by using lenses with a short focal length, meaning the lens is very close to the specimen.
The maximum useful magnifiction of a conventional light microscope is between 500 and 1000 times the NA of the objective lens. |
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Definition
A measure for a microscope found by substituting into the equation for resolving power the minimum possible wavelength and the highest possible NA.
A conventional microscope will get a value slightly less than 0.2μm. This is sufficient to see large cell organelles such as nuclei and mitochondria. The human eye gets around 0.1 mm. |
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Definition
Optical flaws that occur when using a light microscope. They make it impossible to reach the theoretical levels of magnification or resolution.
In order to minimize aberrations objective lenses are made of a series of lenses. The first one magnifies the image, and the rest compensate for errors. |
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Definition
The ability of a specimen to be observed. This depends mainly on contrast. |
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Definition
In order to be visible, an object needs this with its background. You may achieve this by staining a specimen. |
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Definition
A molecule featuring a chromophore (usually an aromatic ring) that absorbs part of a spectrum, making it appear colourful. It is added to a specimen to stain it and give it some contrast when using a light microscope to view it. Some dyes will only stain certain biological molecules, giving another dimension of information to the image. pH is a factor in what molecules a dye may stain. Basic dyes stain by chemical absorbtion. Acidic dyes stain by infiltration and may wash out.
The problem with dyes is that they may be toxic to cells; you can only observe dead cells using them. Some stains cannot penetrate the plasma membrane, so they must be hydrolyzed in acid first, which kills them. |
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Definition
A type of light microscope where the specimen is seen against a bright background. Best suited for specimens with high contrast, such as stained specimens. |
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Definition
An intact specimen, living or dead. Good for small specimens such as single-celled organisms. Bad for larger plant or animal tissues because they are too opaque to be observed with a light microscope. |
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Definition
A type of specimen where the tissue is very thinly sliced. This is good for tissues that make bad whole mounts due to opacity. The cells must first be processed with a fixative. The thinner the section the better. They are made using microtomes for very thin slices. |
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Definition
A chemical used in the processing of tissues before making a section. It rapidly immobilizes all macromolecular material in the tissue, maintaining cell structure.
Includes formaldehyde, alcohol, and acetic acids.
Afterwards the specimen is embedded in paraffin wax to provide mechanical support during sectioning. The wax may be dissolved away afterwards using toluene. |
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Term
Phase-contrast microscope |
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Definition
A type of light interference microscope that makes translucent objects more visible. It does this by converting differences in refractive index into differences in light intensity by first separating the light then making them interfere with each other.
Good for looking at intracellular components of living cells. Motility of organelles may be observed.
They have a handicap in terms of resolution. Images suffer from halos an shading where there are sharp changes in refractive inde. |
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Term
Differential Interference Contrast (DIC) or Normanski Interference |
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Definition
A type of light interference microscope that looks at the change of rate of refractive index across a specimen. The edges of structures where refractive index varies more is seen with good contrast. Gives the image a 3D look. |
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Definition
A type of light microscope that looks at fluorophores inside a specimen. Ultraviolet light shines through a filter so that only wavelengths effecting desired fluorophores goes through. They then appear brightly coloured against a black background. |
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Term
Fluorophore or Fluorochrome |
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Definition
A molecule that absorbs UV radiation and releases a portion of it as visible light, making it appear to glow. This is called fluorescence. They may covalently link to antibodies for immunofluorescence. |
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Definition
When fluorophores covalently link to antibodies that can locate specific proteins in a living cell. Can also be used to locate DNA or RNA molecules containing specific sequences, study molecules that pass between cells, or to determine the calcium ion concentration in the cytosol. |
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Definition
The scientist who in the 1960s discovered how Aequorea victoria jellyfish glow in the ark. He found there was a glowing protien, green fluorescent protein (GFP). He was able to purify the protein. He won the Nobel Prize. |
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Term
Crystal Jelly/Aequorea victoria |
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Definition
A species of jellyfish that glows. This is due to the presence of GFP protein. |
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Term
Green Fluorescet Protein (GFP) |
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Definition
A 238 amino acid, barrel-shaped protein that glows green by reflecting ultraviolet radiation in the form of visible light. It is resistant to denaturation. It is found naturally in Aequorea victoria jellyfish. It may be encorporated into the genes of other animals. It can be used to study the dynamics of proteins in living cells by combining this protein with the protein being studied. The chimeric protein functions in the cell normally, but glowing.
There are other varieties of glowing proteins in different colours including BFP (blue), YFP (yellow), and CFP (cyan). |
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Term
Douglas Prasher, Martin Chalfie, and colleagues |
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Definition
The group of scientists who in the 1990s were able to genetically incorporte the gene for GFP into other organisms. Chalfie won the Nobel Prize but Prasher did not and instead became a shuttle-bus driver after donating all his findings to the world. |
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Definition
A scientist from University of California who developed forms of glowing proteins other than green including BFP (blue), YFP (yellow), and CFP (cyan) as well as DsRed, mBanana, mTangerine, and mOrange. He won the Nobel Prize. |
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Definition
A fluorescent protein discovered in a sea anemone. It may be used in a similar was to GFP. It has variants in diferent colours mBanana (yellow), mTangerine (light orange), and mOrange (orange). |
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Term
Fluorescence/Forster Resonance Energy Transfer (FRET) |
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Definition
An instrument which measures the distances between fluorophores on a nanometer scale. When two protein groups are in close proximity, the excitation energy of the fluorophores may transfer between them. The efficiency of the transfer decreases as they get farther apart. This device measures that efficiency. Used to study the changes in living cells. It is used to look at protein folding, and membrane association/dissociation. |
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Definition
May be used to look at large amounts of data such as hundreds of microscope readings or DNA sequences. It finds patterns or specific genes much quicker and with more accuracy than any human could. Also, this would be a very tedious job for a human.
It can also remove blurry background in images, or change differences in brightness into differences in colour, making an image easier to read.
They may take a series of 2D images to create a 3D model. |
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Term
Charge-Coupled Device (CCD) |
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Definition
A type of video camera that is very sensitive to light, allowing it to film specimens at very low illumination.
This is good for observing living specimens, which may be damaged by excessive light. Also good for looking at fluorescently stained specimens. It can pick up tiny details that a human eye would not pick up. The images are easily transfered into digital images to feed to a computer. |
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Definition
The person who invented the confocal microscope in 1950s. |
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Term
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Definition
A type of light microscope with a pinhole aperature in front of the camera. Only light from a finely focused laser illuminating a very thin layer of the specimen can pass through. This reduces blurriness from other layers of focus. The smaller the pinhole, the thinner the layer of focus, but dimmer the light appears. They are used in fluorescence microscopy. |
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Term
Transmission Electron Microscope (TEM) |
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Definition
A microscope that uses electrons passing through a specimen to form an image. It is a large hollow tube with a vacuum in it through which electrons are accelerated through a specimen at the bottom. The electron rays are focused by electromagnetic lenses. A single objective lens magnifies the image. They can achieve a resolution power many times greater than that of a light microscope. Resolution can be adjusted by the speed of the electrons, using voltage.
λ = √(150/V)
λ = wavelength in Å
V = voltage in volts
They may operate between 10,000 and 100,000 volts. eeven at low power the resolution is theoretically 0.03 Å. In reality aberrations make it 3 to 5 Å, which is still better than a light microscope.
Electrons only bounce off of heavy metals, so specimens must be stained with a heavy metal, which may form an artifact. Fixatives used are glutaraldehyde and osmium tetroxide, which react with amino groups and lipids respectively. The specimens are cut extremely thin (0.1μm max) by a machine. Uranyl acetate, lead citrate, or metal-tagged antibodies.
Other fixation techniques include cyrofixation or freeze-fracture replicaton. |
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Term
Stochastic Optical Reconstruction Microscopy (STORM) |
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Definition
Uses photoswitchable fluorescent proteins, allowsing to localize individual fluorescent molecules with a resolution less than 20 nm! This is done by randomly activating a small number of molecules. They appear as a spot several nanometers wide, when in fact they are much smaller. |
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Term
Scanning Electron Microscope (SEM) |
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Definition
A microscope which uses electrons that have bounced off of the specimen. Electrons are accelerated at the specimen as a fine beam. They bounce of the specimen and hit a detector which forms the image. This gives information on the topography of the surface of the specimen. May be used for objects as small as bacteriophages and as big as animals (mostly bugs).
The specimen cannot have any fluids in order to be scanned. This limits the kinds of specimens that can be looked at. Critical-point drying is used to dry the specimen.
It can magnify from 15 to 150,000 times. Resolving power can be as small as 5μm. The depth of focus is 500 times that of a light microscope. |
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Term
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Definition
A coagulation of heavy metal in a specimen dyed for observation under a TEM. The best way to determine if a structure is one or not is to look at the same cell type fixed in an alternative way. |
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Term
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Definition
A fixation technique for TEM specimens. The specimen is rapidly frozen. This way they don't have to use chemicals or be embedded in resins. This avoids the formation of artifacts, however ice crystals can form unless the water is vitrified properly.
Small specimens are plunged into very cold liquids such as liquid propane. Large specimens undergo high-pressure freezing with jets of liquid nitrogen. The high presure reduces the freezing point of water and thus the formation of ice crystals.
This method of fixation is used by pathologists. |
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Term
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Definition
The process of freezing water so quickly that no ice crystals form. If a specimen under cyrofixation does not undergo this, the ice crystals will destroy cell structure. |
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Term
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Definition
A 3D image generated by a computer from TEM images taken using cyro-ET. |
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Term
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Definition
A scientist from the Max-Planck Institute who invented cryo-ET. |
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Term
Cyroelectron Tomography (Cyro-ET) |
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Definition
A method of using a TEM on unfixed, fully hydrated, flash-frozen cells. You can see 3D structure of the cell in high resolution and use computer programs to make a tomogram. |
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Term
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Definition
A method used in TEM imaging where everything except the specimen is stained, making the specimen relatively bright on the viewing screen. |
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Term
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Definition
A method of TEM imaging where the specimen is placed in a vaccum and sprayed with a heavy metal at an angle. In spots where there is no heavy metal it appears lighter. The values are reversed, and they appear darker, making them look like shadows. This gives the image a 3D effect. |
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Term
Freeze-fracture replication |
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Definition
A fixation technique used for TEMs where a specimen is flash-frozen then split with a knife. The crack goes through a cell, revealing inner structure. A heavy metal is applied to the open crack and a replica is made of the specimen using carbon.
Good for looking at membrane structures; the crack will always follow the path of least resistance, revealing membranes. |
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Term
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Definition
A modified version of freeze-fracture replication where after the cell is slpit it is heated inside a vaccum, causing the top layer ice to subliminate, giving a higher relief to the crack which is then sprayed with a heavy metal. |
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Definition
The person who discovered deep-etching. |
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Definition
A technique of TEM specimen fixation where even more ice is removed from a freeze-fractured specimen than in freeze etching. |
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Definition
A method of SEM specimen preparation where the specimen, after being put through a series of alcohols, is treated to a temperature and pressure combination that is exactly equal to the density of the vapour of the liquid being removed from the specimen. At this point there is no surface tension to the liquid, so it evaporates without distorting anything in the specimen. After this it is coated with a heavy metal. |
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Term
Atomic Force Microscope (AFM) |
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Definition
A high resoltion scanning instrument where a physical tip scans and object. It oscillates and "feels" variations in topography of the specimen. The information is then turned via computer into a 3D model of the surface of the specimen.
It can determine the exact molecule in the field, where other methods can only determine the average molecule. It may be used to test the mechanical properties of molecules. Ligands may be attached to the tip to test for a substances affinity to the ligand. |
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Term
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Definition
The distance between the nearest and farthest objects that appear sharp in a microscope image. |
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Term
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Definition
The smallest point a light microscope can detect. It appears to be an airy-looking disk. Resolution is defined by the distance between two distinguishable airy disks. |
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Definition
The crest-to-crest length of one wave of electromagnetic radiation (light). The resolution of a light microscope is dictated by this; shorter wavelengths can achieve greater resolutions than larger ones. |
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Definition
The theoretical maximum amount of resolution a light microscope can achieve. In reality it is impossible to achieve due to aberrations. |
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Term
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Definition
To make an object appear larger using lenses. |
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Definition
A dye that changes colour when it comes into contact with a particular cell structure. Toluidine Blue O is metachromatic. |
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Term
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Definition
A metachromatic dye. Pectins stain pink, lignins stain blue or green, and at high pH, nucleic acids stain blue-green. |
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Term
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Definition
A stain used when the first stain does not stain all the structures, or doesn't stain structures sufficiently enough. |
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Term
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Definition
A stain that does not kill the cells it stains. Used for micro-organisms or tumour cells which may be cultured for a long period.
Trypan blue, propidium iodine. |
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Term
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Definition
A stain that does not kill the cells it stains. Used for tissue cells that have recently been removed from the body and need to be observed before they die. Tryptan blue, propidium iodine. |
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Term
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Definition
Different from luminescence. When a molecule or molecule complex absorbs light from the non-visible spectrum (ultraviolet) and reflects it in the visible spectrum, making it apper to glow. |
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Definition
When a fluorescent molecule or complex loses its fluorescence due to damage from intense light or chemicals. |
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Definition
A photoconvertible protein which changes fluorescence from red to green based on the wavelength of light it is exposed to.
Used to track individual cells/structures in a larger system. |
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Definition
An image of a brain created in 2007 by Lichtman and Sanes Labs that used different ratios of fluorescent proteins on brain neurons, making a stunning image of hundreds of differently coloured neurons. |
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Definition
A retrieval signal for soluble ER proteins. It is the sequence Lysine, Aspartic acid, Glutamic acid, Leucine. An ER residence protein outside the ER with this tag will be returned to the ER via COPI-coated vesicles. If you delete the sequence, they never return. If you add this sequence to any protein, it will reside in the ER. |
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Term
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Definition
It is stable, flexible, and capable of self-assembly. It is 6 nm thick. It is a lipid bilayer of amphipathic lipids with hydrophilic heads on the outside and hydrophobic tails on the inside. If you drop pure amphipathic lipids in water, small, empty liposomes of water will form. Each leaflet has a unique composition of lipids and proteins.
A cell membrane encloses the cell and all its compartments, controls movement in and out of the cell, detects external stimuli, and interacts with neigbhoring cells. Different membranes feature different proteins for their different functions.
They cannot form spontaneously, they are only expanded by inserting lipids and proteins. |
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Term
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Definition
The outer membrane of a cell. It is 5 to 10 nm thick. Discovered in the 1950s when it was successfully dyed. Under a microscope it appears to have 3 layers: two outer darkly dyed layers and one inner lightly dyed layer.
It is supported by a skeleton made from spectrin, ankyrin, and actin. The cytosolic layer has high levels of PI(4,5)P2. This helps recruit proteins for clathrin-coated vesicle formation. |
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Definition
The scientists who in 1925 determined that the plasma membrane was two layers of lipids. They did this by analysing the membrane of an amount of blood cells (which lack nuclei and have minimal extra membrane). They spread the lipid over water and measured the surface area and compared it to the calculated membrane area for the blood cells. The ratio was always near 2:1. This lead them to believe the membrane was a bilayer. |
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Definition
The scientists who in 1935 determined that cell membranes were studded with proteins. |
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Definition
The scientists who in 1972 developed the fluid mosaic model. |
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Term
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Definition
A model which says that a biological membrane has proteins stuck in it and they can move about laterally on the membrane and interact with each other freely.
The concentration and type of proteins is different based on the type of membrane it is. |
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Term
Integral/transmembrane proteins |
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Definition
Proteins that penetrate the cell membrane all the way through; they have components on each side of the membrane.
Produced co-translationally into the ER membrane. The translocon opens to the side to let it out into the membrane. Proteins with multiple trans-membrane segments are strung through like a sewing machine. The polypeptide sticks to the translocon in a way to correctly orientate it in the membrane. The N-terminus may be inside or outside of the lumen. |
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Definition
A protein which does not have any components in the cell membrane, but is associated with the surface of the membrane. Produced by free ribosomes and deposited into the cytosol. |
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Term
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Definition
A protein which has hydrophobic components embedded in one leaflet of the cell membrane. |
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Term
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Definition
Non-polar. Does not dissolve in water. |
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Term
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Definition
Polar. Dissolves in water. |
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Term
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Definition
Having hydrophobic and hydrophilic regions. |
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Term
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Definition
Proteins attached in some way to a biological membrane. Different cells and structures vary in the amount and representation of proteins. Feature meets form.
Most can move laterally along their leaflet, but to flip to the other leaflet requires an enzyme. |
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Term
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Definition
A sheath of many layers of membranes surrounding a nerve cell. It has a very low concetration of proteins and serves to insulate the neuron for optimal electrical signaling. The membrane is high in glycolipids, especially galactocerebroside. It has plasmalogens. Abnormalities in it can cause neurological dysfunciton. |
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Definition
The membrane surface which is in contact with the extracellular space in a polar secretory cell. It excretes materials into a duct. It features many integral proteins. It as a specific sorting signal for secretions. |
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Term
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Definition
The membrane surface of a secretory cell which is in contact with other secretory cells. It has interactions with other cells. It features many integral proteins. |
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Term
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Definition
The membrane surface in contact with the blood system in a secretory cell. Nutrients are taken up through this surface. It as a specific sorting signal for secretions. |
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Term
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Definition
An important feature of biological membranes. It depends on the composition (saturated vs. unsaturated) of the membrane as well as the temperature and concentration of cholesterol. A balance provides mechanical support as well as flexibility. It must allow proteins to interact while not being permeable. Temperature differences are not an issue to mammals and birds, who are warm blooded. It is especially a problem for fish that live in cold water. Organisms such as these have to adjust their membrane lipid components by either forming double bonds (using desaturase) or shuffling the chains on lipids (using phospholipase). Over a long period of time only the correct lipids are made. |
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Definition
The term used to describe a biological membrane when it is warmed past its transition point. It is more liquid than a crystalline gel. The molecules form a specific orientation as a membrane, but they can rotate and move laterally. |
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Term
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Definition
A term used to describe a biological membrane when it is cooled past its transition point. The molecules are more restricted and it is more solid than a liquid crystal. |
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Term
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Definition
The temperature point when a biological membrane becomes liquid crystal (warm) or cyrstalline gel (cold). It is effected by the saturation and length of the fatty acids in the membrane. Saturated and longer fatty acids have a higher transition point. Cholesterol makes it less extreme. |
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Term
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Definition
A region of the biological membrane which is high in PC and cholesterol, causing it to "float" a little above the other lipids. GPI-anchored proteins concentrate in this region. They form in synthetically made membranes. May form a functional compartment for protein interaction. Their existence in cells is debated. |
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Term
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Definition
The point after which images become hazy in a light microsope. For conventional light microscomes this is around 0.2 μm. |
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Term
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Definition
When a person has less than the normal amount of rods in their eyes, making it impossible for them to differentiate between certain colours. |
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Term
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Definition
When a person has more than the normal amount of rods in their eyes. This allows them to see colours regular people cannot. |
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Term
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Definition
A test using a dye which is used to classify bacteria. There are gram positive and gram negative bacteria. |
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Term
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Definition
A sequence of hydrophobic amino acids on a protein up to 20 amino acids long which acts as an "address" in a postal system; it tells the protein where it is meant to go. Each organelle has an address and proteins may be sent to it.
It may be on either end of a protein.
During protin synthesis this sequence is made first (on the amino terminus) and directs the ribosome if and where to attach to the RER. |
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Term
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Definition
A protein with a part on it added by scientists, such as signal sequences or fluorescent sections, by altering the genes of the organism, using a virus such as VSV. A plant can have up to 5 of these altered protein at a time. |
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Term
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Definition
A device used to make very thin sections. The sections then float in water. Wax is more commonly used today. The device is not used much anymore due to better technologies. |
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Term
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Definition
A device used to flash-freeze specimens. |
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Term
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Definition
"False foot". The extensions of membrane from an amoebea. They aid in phagocytosis. Even amoebas do have a specific shape they adhere to. |
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Term
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Definition
All the bonds are single bonds. When in lipid membranes they pack more closely together, producing more solid membranes (crystalline gel). The more of this a membrane has, the higher its transition temperature is. |
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Term
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Definition
Contains some double bonds. When they are cis they form membrane lipids that don't pack very well with each other, producing more fluid membranes (liquid crystal). The more of this a membrane has, the lower its transition temperature is. |
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Term
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Definition
Ruffle shaped membranous structures on the outside of cells. Used to grab ahold of neighboring cells. If nothing can be found to grib, they recede. |
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Term
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Definition
A bilayer of amphipathic phospholipids with the hydrophobic tails facing inwards and hydrophobic heads facing outwards. Continuous, unbroken sheets. The plasma membrane is one. It serves to compartmentalize eukaryotic cells into organelles, keeping chemical reactions from occuring between substances on either side of it, and encouraging chemical reactions of substances on same sides.
It is selectively permeable. Prevents unrestricted exchange but allows some exchanges. |
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Term
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Definition
The person who in the 1890s determined that cells were surrounded by a lipid component. From the University of Zurich. Diffused different solvents through the root hairs of plants. Discovered that fat-soluble substances diffused faster. |
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Term
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Definition
The most common type membrane lipid. A phospholipid. Includes phosphatidic acid, PC, PE, PS, and PI. A diglyceride. It has a phosphate group esterfied to its third hydroxyl group. A hydrophilic head group may be attached to this. |
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Term
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Definition
A lipid with two fatty acids esterfied to the glycerol backbone's hydroxyl groups. |
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Term
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Definition
A lipid with all three hydroxyl groups of the glycerol backbone esterfied to fatty acids. They are not ampipathic, and cannot be found in the lipid membrane. |
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Term
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Definition
A phosphoglyceride with no additional functional groups. It is very rare in most membranes. |
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Term
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Definition
A phosphoglyceride with a choline group. It has a neutral charge at normal pH levels. |
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Term
Phosphatidyethanolamine (PE) |
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Definition
A phosphoglyceride with an enthanolamine group. It has a neutral charge at normal pH levels. |
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Term
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Definition
A phosphoglyceride with a serine group. It has a negative charge at normal pH levels. |
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Term
Phosphatidylinositol (PI) |
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Definition
A phosphoglyceride with an inositol group. It has a negative charge at normal pH. |
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Term
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Definition
The hydrophilic portion of a phosphoglyceride that attaches to the phosphate group. It determines what kind of phosphoglyceride it is. |
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Term
Ethyl Eicospentaenoic Acid (EPA) |
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Definition
A highly unsaturted omega-3 fatty acid found in fish oil which has supposed health benefits. It has 5 double bonds.
May be in the fatty acids of PE or PC in the brain or retina. |
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Term
Docosahexaenoic Acid (DHA) |
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Definition
A highly unsaturate fatty acid found in fish oil with supposed health benefits. It has 6 double bonds.
May be in the fatty acids of PE and PC in the brain and retina. |
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Term
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Definition
A type of amphipathic membrane lipid. A ceramide with various additional groups esterfied to the terminal alcohol of the sphingosine. The fatty acids tend to be longer than in phospholipids. |
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Term
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Definition
A component of a sphingolipid. A sphingosine (an amino alcohol) with a very long hydrocarbon chain linked to the amino group. |
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Term
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Definition
A sphingolipid with a phosphorycholine group. This is the only molecule in the lipid membrane without a glycerol backbone. One of the only membrane lipids not made in the ER. |
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Term
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Definition
A sphingolipid with a carbohydrate group. They are in high concentration in the nervous system, such as in myelin sheaths. One of the only membrane lipids not made in the ER. |
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Term
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Definition
A glycolipid with a simple sugar group. |
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Term
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Definition
A glycolipid with a small cluster of sugars including sialic acid. When viruses enter their target cells, they first bind to gangliosides in the cell membrane. |
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Term
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Definition
A cerebroside with galactose attached to the ceramide group. It is in high concentration in myelin sheaths. Mice who are unable to produce it suffer from neurological diseases, seizures, and blindness. |
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Term
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Definition
A component of certian cell membranes. A sterol. It can be up to 50% of the lipid molecules in some animal plasma membranes. Plants lack it. The hydrophilic hydroxyl group lays towards the outside of the membrane surface with the rest of the molecule embedded in the membrane. It has rigid, hydrophobic rings which stiffen the membrane while maintaining its fluidity. It is important to maintaining membrane fluidity by normalizing the transition point. It makes the membrane more durable. It is evenly distributed between the two membrane leaflets. It is a precursor to steroid hormones. It is transported through the blood in LDLs. |
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Term
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Definition
Determined using mass spectrometry. It effects the physical properties of the membrane and protein activity. |
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Term
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Definition
A synthetically made vesicle made from mixing a purified membrane lipids and proteins, such as PC, with water. Used to study membrane proteins, and to deliver drugs or DNA to cells. The walls need to contain antibodies in order to not be regected by the cell. |
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Definition
An enzyme which desaturates (makes unsaturated) fatty acids in a membrane. This is to lower the transition point of the membrane. |
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Term
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Definition
An enzyme which shuffles the fatty acids in a membrane. It removes the fatty acid from the glycerol and acyltransferase (another enzyme) transfers it to a different phospholipid. This can reduce or increase the transition point. |
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Term
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Definition
The total movement of a substance in or out of a cell the difference of influx and efflux. Occurs either through the lipid bilayer or through a protein-lined channel. May be passive or active. |
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Term
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Definition
The movement of a substance into the cell. |
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Term
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Definition
The movement of a substance out of a cell. |
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Term
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Definition
When a molecule passes into or out of a cell along its concentration gradient. No help is required from the cell. May pass through the lipid membrane or a protein-lined pore, depending on its partition coefficient and size (smaller molecules pass though faster). O2, CO2, NO, and H2O pass through the lipid bilayer readily. |
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Term
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Definition
A measure of a substance's solubility in a nonpolar solvent such as octnol or vegetable oil. The greater this value is, the faster it will penetrate the lipid bilayer. Substances where this number is low must pass through a protein pore. |
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Term
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Definition
When a substance moves into or out of a cell against its concentration gradient. Requires a protein pore to actively pump it, using ATP. |
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Definition
The person who proposed the endosymbiont theory. From Boston University. |
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Term
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Definition
The theory that mitochondria and chloroplasts are the adapted forms of ancient prokaryotes that were engulfed by larger eukaryotes very long ago. No-one can prove this. Mitochondria were once aerobic heterotrophic prokryotes engulfed by a larger anaerobic prokaryote, which then became a eukaryote. This benefitted the large cell because it could now breathe oxygen. Chloroplasts were once cyanobacteria which were engulfed by a eukaryote. This benefited the eukaryote because if could now photosynthesize. |
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Definition
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Term
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Definition
Cannot make its own food; must take compounds in from the environment. |
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Term
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Definition
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Term
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Definition
A smaller cell living inside a larger cell. In the Endosymbiont Theory, mitochondria and chloroplasts are endosymbionts with traits adapted for living inside cells. |
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Term
Emile Zuckerkandl and Linus Pauling |
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Definition
The scientists who in 1965 came up with a new taxanomic scheme based on genetics rather than on physiological characteristics. Measured how distantly organisms were related by comparing proteins and nucleic acids. They were able to devise an evolutionary timeline and a phylogenic tree this way. |
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Term
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Definition
The membranes found inside a eukaryotic cell. Includes ER, Golgi body, lysosomes, vacuoles, and vesicles. Its surface area is much greater than the plasma membrane's. Evolved from internalized portions of the plasma membrane. It is a cell-wide system for producing, modifying, and transporting substances. Parts differ in proteins, activities, and structure. There are secretion and endocytic pathways. |
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Term
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Definition
A substance's pathway where it is produced by the cell and taken to where it needs to be. Starts in the ER, moves to the Golgi complex, then it is exported to various destinations. May be constitutive or regulated. May be secretory. |
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Term
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Definition
A biosynthetic pathway that occurs continutally in a cell. The cell is always producing and secreting a substance. |
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Term
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Definition
A biosynthetic pathway where materials are stored in the cell as granules until there is a specific stimulus. |
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Term
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Definition
The pathway a substance takes as it is imported by the cell from the outside. It is used for importing particles too large to take a trans-membrane route. The membrane first invaginates in endocytosis or phagocytosis. |
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Term
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Definition
A technique of looking at cells where materials are labeled with radioactive isotopes and tracked in a cell. |
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Term
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Definition
A short incubtion period of a cell in a radioactive isotope (pulse) followed by viewing with a microscope (chase). Only some of the proteins are marked, allowing to track particular substances through the cell.
This was abandoned in 1994 when the use of fluorescent proteins came about. Radioactive substances are dangerous. |
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Term
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Definition
The breaking up of cells to isolate organelles. Oraganelles are broken up into 100 μm wide vesicles to form a cell free system. The vesicles are then sorted with subcellular fractionation. Used to study the molecular composition of organelles. Became popular in the 1960s. |
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Term
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Definition
An amount of cells that have been homogenized. There are no whole cells, only organelles. The organelles are broken up ito vesicles around 100 μm wide. |
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Term
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Definition
Looking at mutations that occur in organisms in order to determine the exact function of various proteins. Only one protein changes at a time. When this protein consistently cannot function or is made improperly we can look to see what goes wrong in the cell to learn the protein's function. Researchers have found mutants for every step of the secretory pathway; the genes for each protein cloned and sequenced. |
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Term
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Definition
The space inside an organelle. |
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Term
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Definition
Flattened sacs of membrane found in the ER. |
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Term
Peri-nuclear endoplasmic reticulum |
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Definition
The region of the ER close to the nucleus. Mostly rough. |
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Term
Cortical endoplasmic reticulum |
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Definition
The portion of the ER far away from the nucleus. |
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Term
Rough Endoplasmic Reticulum (RER) |
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Definition
ER with ribosomes in the membrane. Mostly in the peri-nuclear ER. It is mostly cisternae and it is continuous with the nuclear envelope. It produces, modifies, and transports proteins, including membrane proteins and products of glycosylation. It is the strting point of the secretory pathway. It has chaperone proteins, which the SER does not. |
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Term
Smooth Endoplasmic Reticulum (SER) |
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Definition
ER that lacks ribosomes in its membrane. Mostly the tubular elements and smooth vesicles. It synthesizes steroid hormones, detoxifies from many organic compounds, metbolizes carbohydrates, and sequesters calcium ions in the muscle cells. Release of calcium ions triggers muscle contraction. It has reticulons, which the RER does not. It uses cytochrome P450 to detoxify. Ethanol abuse can lead to its proliferation. |
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Term
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Definition
Spindle shaped organelles found in the ER during cellular stess. 10 to 15 μm long. Act as defense mechnisms when the cell is attacked. |
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Term
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Definition
Ribosomes in the cytoplasm. They create cytosolic, cytoskeletal, and peripheral proteins as well as proteins destined for the nucleus, peroxisomes, mitochondria or chloroplasts. Two thirds of proteins in mammals are produced this way. Proteins are released directly into the cytosol. Peroxisome, chloroplast, and mitochondria proteins are imported to their organelle post-translationally. |
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Term
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Definition
Messenger RNA. DNA is translated into pre-mRNA then into mRNA which is then strung through ribosomes to make proteins in the cytoplasm and ER. In prokaryotes it is the primary transcription. In eukaryotes, it is a modified RNA with the introns removed. |
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Term
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Definition
mRNA is strung through a ribosome in the cytoplasm, translating into a protein. Some proteins are produced co-translationally on the RER. |
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Term
Co-translational protein import |
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Definition
Produces proteins that are immediately deposited into the ER or ER membrane via a translocon. One third of proteins in mammals are produced this way. May produce secretory proteins or integral membrane proteins. Signal sequences are produced first in the cytosol and bind to SRP, which halts production and binds to a SRP receptor near a translocon. The SRP unbinds, allowing protein translation to continue, displacing the plug in the translocon. The signal sequence is removed and replaced by a carbohydrate. |
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Term
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Definition
Found on the RER membrane. A protein pore of 2 to 4 segments to wich ribosomes attach and polypeptides are strung. There is an SRP receptor by it to bind to incoming ribosomes. When not in use it has a plug blocking it. The naschent polypeptide pushes it away. Integral membrane proteins are pushed out to the side into the membrane. |
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Term
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Definition
A soluble protein produced co-translationally. It is strung through the translocon and deposited into the ER lumen for further processing. |
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Term
Signal Recognition Particle (SRP) |
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Definition
A G protein which binds to the singal sequence of a nascent protein as it emerges from the ribosome. This halts translation and then it binds to an SRP receptor near a translocon and unbinds so that protein production can continue co-translationally. |
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Term
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Definition
The term used to describe a molecule such as a polypeptide or mRNA when it is still being constructed and is only partially complete. |
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Term
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Definition
A protein found in the ER which allows newly formed soluble proteins to fold properly and/or transports them to where they need to be. BiP is one. |
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Term
Transmembrane Domain (TMD) |
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Definition
The hydrophobic domain of an integral membrane protein which is found in the membrane. One protein may have multiple. Often they are helical in shape. |
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Term
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Definition
A round sac of membrane containing contents to be transported somewhere. May be transporting integral proteins in its membrane. There are smooth and rough vesicles associated with the smooth and rough ER. When it gets to its destination it fuses with it, depositing contents and membrane. They move along the cytoskeleton, moved by motor proteins. |
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Term
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Definition
When a donor vesicle makes a rounded lump-shaped protrusion which gets rounder until a protein "snips" it off into a vesicle. Contents, membrane proteins, and membrane composition are all selective. During this process the vesicle is coated with soluble proteins that accumulate on the outer layer, forming a coated vesicle. |
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Term
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Definition
When a cell has a particular direction in which the secretory/endocytic pathways are moving. Secretory cells have this. Cells can sense gravity; this effects polarity. |
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Term
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Definition
A biosynthetic pathway which ends in the substance being exported to outside the cell by fusing vesicles with the plasma membrane. |
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Term
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Definition
A large, densely packed storage vesicle waiting for a hormone or nerve impulse signal before being fused with the plasma membrane, secreting its contents. It becomes dense after leaving the TGN. |
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Term
James Jamieson and George Palade |
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Definition
The scientists from Rockefeller University who used autoradiooography to study cells. They labelled amio acids with radioactive materials and put them into living pancreatic tissues in order to track the path of proteins being produced. |
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Term
Vesicular Stomatitis Virus (VSV) |
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Definition
A virus used to encorporate GFP genes into a cell. It turns the cell into a GFP factory, allowing us to look at protein synthesis. |
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Term
Albert Claude and Christian De Duve |
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Definition
The scientists who in the 1950s and 60s came up with cell homogenization and subcellular fractionation. They analyzed the molecular composition of various organelles. |
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Term
Subcellular fractionation |
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Definition
In cell homogenization this is the step after the organelles are broken up where they are sorted using a centrifuge. Once sorted, each organelle can be studied individually. Proteins may be extracted and analysed with mass spectrometry. |
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Term
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Definition
A tiny vesicle formed from the homogenization of the ER. Separated from the other organelles using subcellular fractionation. Ones from the RER and SER can be separated. |
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Term
George Palade, Philip Siekevitz, and colleagues |
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Definition
The scientists from Rockefeller University who stipped RER microsomes of their ribosomes and determined they were capable of forming proteins in vitro when given the correct ingredients. When attached to microsomes, the proteins are deposited inside the microsome lumen. |
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Term
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Definition
The act of remaking a biological structure from purified substances in vitro. We have made vesicles by incorporating bud-promoting protiens and cargo-recruiting proteins into a liposome. |
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Term
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Definition
An organism or cultured cell whose chromosomes contain abnormal genes caused by DNA replication errors. The cell then functions differently than it should. Used in mutant analysis. They can be "cured" by incorporating correct DNA sequences. |
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Term
Randy Schekman and colleagues |
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Definition
The scientists from the University of California who used mutant analysis to study secretions in yeast cells. Yeast can be cultured as a haploid, helping in mutant analysis. In diploid cells if one set of DNA is wrong, the other set may be used, causing no mutation. |
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Term
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Definition
A process where cells produce RNA that binds to mRNA, inhibiting protein translation. In this way, you can block the production of any protein. |
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Term
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Definition
A membrane folding protein found in the SER but not the RER. |
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Term
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Definition
A family of oxygen-transferring enzyme found in the SER which can detoxify many different compounds. They lack substrate specificity.
Black charr on cooked meat turns carcinogenic when oxidized.
It is found in many medications. Genetic differences in naturual detoxification is why some people react differently to medication than others.
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Term
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Definition
A cell which secretes proteins on a regular basis. Acinar cells, pancreatic cells, intestinal mucus secreting cells, hormone secreting endocrine cells, and liver cells. They have a distinct polarity and an enlarged RER near the basal surface. Secretory granules are kept near the apical surface. The apical surface faces a duct which carries the secreted substances away. |
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Term
Gunter Blobel, David Sabatini, and Bernhard Dobberstein |
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Definition
The scientists from Rockefeller University who in the 1970s discovered that the N-terminal portion of a protein (its signal sequence) is the first part to emerge from a ribosome. |
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Term
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Definition
The path that peroxisome, chloroplast, and mitochondria proteins take on their way to their organelles. Used more commonly in yeast than in mammals. |
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Term
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Definition
A protein that may be bound to GTP or GDP, high and low energy states. This effects its abilities to bind to other proteins. It acts as a "molecular switch" in many cell functions, such as in co-translational protien synthesis. |
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Term
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Definition
An integral membrane enzyme associated with translocons that removes the signal sequence of a nascent protein as it passes through a translocon. |
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Term
Oligosaccharyltransferase |
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Definition
An integral membrane enzyme associated with translocons which adds a carbohydrate to the N-terminus of a nascent polypeptide right after signal peptidase removes the signal sequence. |
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Term
Protein Disulfide Isomerase (PDI) |
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Definition
An enzyme which aids in protein folding by joinging together cystein groups to make disulfide bridges. |
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Term
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Definition
The enzyme that flips half of membrane lipids to the inner leaflet. The enzyme that makes membrane lipids can only put them on the outer layer. |
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Term
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Definition
A protein which transports membrane lipids from one membrane to the other via the cytosol. Membranes may also be transported by transport vesicle. |
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Term
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Definition
The carbohydrate group on a glycoprotein. The sugar sequence is very specific. It is attached to the protein on a specific amino acid sequence. It is produced separately from the protein on dolichol phosphates and added by oligosaccharyltransferase. It aids the protein in proper folding. They are produced by glycosultransferases. May be N-linked or O-linked. |
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Term
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Definition
Enzymes that build oligosaccharides. Their specific sequence in the ER lumen determines the oligosaccharide sequence. |
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Term
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Definition
The substance on which oligosaccharides are made by glycosultransferase before they are added to nascent proteins. |
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Term
Congenital Diseases of Glycosylation (CDGs) |
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Definition
Diseases caused by mutations in the glycosylation processes of glycoproteins. They may be effectively treated with a simple mannose supplement. |
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Term
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Definition
After a protein and folded it is screened for defects in the ER. If it is improperly formed it detected by its hydrophobic regions and is sent back to be refolded. This is repeated until it is in its native state. Too many tries results in the protein being destroyed. |
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Term
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Definition
The sequence and shape of a protein when it is properly formed and folded. |
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Term
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Definition
The process of destroying incorrectly formed or folded proteins in the cytosol. Oligosaccharides are removed and the protein is acted upon by proteasomes. |
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Term
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Definition
Machines that destroy incorrectly formed or folded proteins using ERAD. They are hollow and cylindrical with two regulatory particle caps. The hollow space is 13 Å wide. It has 4 rings, each made from 7 polypeptide subunits. The rings go α, β, β, α. The protein is strung through and degraded using ATP energy. |
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Term
ER-Associated Degradation (ERAD) |
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Definition
The process carried out by proteasomes where incorrectly formed or folded proteins are destroyed. Ensures there are no incorrect proteins in the cell. |
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Term
Unfolded Protein Response (UPR) |
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Definition
When incorrect proteins are produced at a rate which the proteasomes cannot handle, a series of signals result in the production of more chaperones, transport proteins, and protein destroying proteins. Key amino acids are phosphorylated to prevent any more incorrect proteins from forming.
It can lead to the death of the cell. When the cell recieves suicide signals, it may undergo this even if there are no incorrect proteins. |
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Term
Vesicular-Tubular Carrier (VTC) |
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Definition
The structure formed when recently budded vesicles fuse together to form tubules and vesicles. They move from the ER to the Golgi through the ERGIC. They fuse with the Golgi. |
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Term
ER Golgi Intermediate Compartment (ERGIC) |
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Definition
The space between the ER and the Golgi complex. Made out of VTCs which move along microtubules. The VTCs move from the ER to the Golgi. |
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Term
Exit site/Transitional element |
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Definition
A region on the RER lacking ribosomes where transport vesicles may form. |
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Term
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Definition
The person who discovered the Golgi complex in 1898. The Golgi complex's name comes from them. He won the Nobel price in 1906. |
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Term
Trans-Golgi Network (TGN) |
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Definition
The region of the Golgi complex furthest from the ER. The cisternae have broken up by this point. It is a series of tubules and vesicles. It sorts proteins and puts them into separate vesicles which go to different cellular destinations. |
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Term
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Definition
Golgi cisternae near the TGN. |
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Term
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Definition
Golgi cisternae between the cis and trans cisternae. |
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Term
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Definition
Golgi cisternae near to the CGN. |
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Term
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Definition
The region of the Golgi complex nearest to the ER. The cisternae are still forming. It is a series of interconnected tubules. It is a sorting station for distinguishing between proteins to be shipped back to the ER or to continue to the rest of the Golgi. |
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Term
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Definition
A group of many Golgi bodies. There may be hundreds of Golgi bodies in one cell. Different cells have different numbers. |
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Term
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Definition
"Forward" motion. Motion from the ER to the Golgi body to the plasma membrane. In the vesicular transport model this is the direction substances move in the Golgi body as they are synthesized. |
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Term
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Definition
"Backwards" motion. Motion from the plasma membrane to Golgi complex to ER. In the cisternal maturation model some vesicles move in this direction down the Golgi complex, maintaining each cisternae's resident proteins. |
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Term
N-linked oligosaccharides |
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Definition
Produced and attached to proteins entirely in the ER. |
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Term
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Definition
Produced and attached to proteins entirely in the Golgi complex. They can be much more complex than N-linked oligosccharides. Mannose residues are removed from oligosaccharides in the cis and medial cisternae and then a series of other sugars are added by glycosyltransferases. |
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Term
Cisternal maturation model |
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Definition
A model for how the Golgi complex moves. This model was accepted until the 1980s when it was challenged by the vesicular transport model. It is now accepted again.
Each cisternae matures into the next one, moving away from the ER. Resident proteins are brought back to the right cisternae by vesicles. Blocking vesicle flow from the ER causes it to desintigrate. The fact that some cisternae have certain proteins is due to retrograde motion. |
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Term
Vesicular transport model |
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Definition
A model for how the Golgi complex moves. It was proposed in the 1980s. Each cisternae stays still and constant, but its contents are continuously transported via vesicles to the next cisternae. |
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Term
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Definition
A series of 3 nucleic acids in mRNA that translate into amino acids. Each codon is read in protein translation to make a specific polypeptide. |
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Term
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Definition
RNA that carries amino acids. It has an anti-codon which recognizes its complementary codon on mRNA, dropping off the correct amino acid. In eukaryotes it is transcribed by RNA polymerase III. |
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Term
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Definition
A part of tRNA that recognizes its complementary codon on mRNA in a ribosome so that the tRNA drops off the correct amino acid every time. |
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Term
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Definition
A scholarly article that explains new discoveries. It has a materials and results section because it is based on actual experiments. |
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Term
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Definition
A scholarly article that makes references to primary articles. It reviews or brings together primary article. No new discoveries are made, but there may be new connections or points. |
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Term
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Definition
A integral membrane found on the plasma membrane. It has 12 helical transmembrane domains. Stored in vesicles until it is activated. It is glycosylated in the Goli. It is found in skeletal and adipose tissue. It is related to insulin. |
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Term
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Definition
The process of attaching an oligosaccharide to a protein. Can occur in the ER or Golgi. Specific amino acids on the protein signal whether and what carbohydrates to be attached. |
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Term
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Definition
The central part of a Golgi cisternae. |
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Term
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Definition
The enzyme which adds sugars to a developing oligosaccharide in the Golgi body. There is a different one in each lumen, so that the sugars are added in the right order. |
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Term
James Rothman and colleagues |
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Definition
The scientist from Stanford University who in 1983 showed using cell-free systems that Golgi cisternae form vesicles that fuse with other Golgi cisternae in vitro. |
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Term
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Definition
When a transport vesicle becomes part of a target membrane, depositing its contents and membrane in the target membrane. The vesicle tethers using Rabs, docks using SNAREs, and fuses. Even after docking, fusion cannot occur until the activating signal, such as Ca2+ ions. |
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Term
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Definition
A vesicle with soluble proteins accumulted on its outer surface. It may have just recently budded. The protein coat aids the vesicle in the budding process: it shapes the bud as well as selecting specific cargo. The coat has two layers: an outer cage and an inner layer of adaptors.
There are COPII, COPI, and Clathrin coats. |
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Term
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Definition
"Coat protein 2". They move materials from the ER in anterograde motion to the ERGIC and Golgi, and from cis to trans Golgi cisternae. The proteins in the coat recognize proteins labelled with "ER export" in their cytosolic tails. Docking proteins and cargo-binding proteins are recruited.
Sar1, Sec 13, Sec23, Sec24, and Sec 31 help in forming the budding shape. |
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Term
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Definition
"Coat protein 1". They move materials in retrograde motion from the Golgi and ERGIC to the ER and from trans to cis Golgi cisternae. They return lost resident proteins to their correct locations. They were discovered by using G proteins that don't convert into GDP form; the vesicles accumulated in the cytosol. Arf1 is in the budding process. |
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Term
Clathrin-coated vesicles (CCV) |
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Definition
They move materials from the TGN to endosoms, lysosomes, and plant vacuoles. They move materials from the plasma membrane to the endocytic pathway. They have an outer honeycomb-like lattice of clathrin. |
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Term
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Definition
"Secretion Associated Ras-related protein 1". A G protein in COPII coats. It is recruited to the donor membrane by GEF in GDP form, then switches to GTP, causing its N-terminal to insert in the outer leaflet, bending the bilayer a little bit. It recruits Sec13, 23, 24, and 31. When it switches back to GDP, the coat disassembles. GDP form has a higher affinity to membrane. |
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Term
Sec13, Sec23, Sec24, and Sec 31 |
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Definition
Proteins involved in the budding of COPII-coated vesicles. They are recruited by Sar1. They are banana shaped, curving the membrane. Sec24 binds with ER export signals. Sec 13 and 31 form the outer cage shape, assembling into a flexible polyhedron. It can be different sizes. |
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Term
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Definition
"ADP Ribosylation Factor 1". A G protein used in the budding of COPI-coated vesicles. It is recruited to the donor membrane in GDP form, when it switches to GTP, attaching to the outer leaflet, curving it. It binds to clathrin and adaptors. It switches to GDP after budding and the coat disassembles. |
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Term
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Definition
Proteins which are only found in certain membranous organelles. They are excluded from budding vesicles by their physical properties, but sometimes they are accidentally taken away by budding vesicles. When this happens they have retrieval signals and they are returned via COPI-coated vesicles. |
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Term
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Definition
Sequences on the C-terminus of residential proteins. It causes them to be returned to their correct compartment by COPI-coated vesicles should they escape somehow. Every compartment has a specific signal, e.g. KDEl and KKXX. |
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Term
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Definition
A retrieval signal for ER membrane proteins. K stands for lysine and X stands for any residue. If a resident ER membrane protein is found outside the ER, it is picked up and returned by COPI-coated vesicles. |
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Term
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Definition
A protein destined for the lysosomes. It is synthesized co-translationally in the ER. When in the Golgi mannose 6-phosphate signal is added to it. It is then recognized by MPRs, which transport it to the lysosomes in clathrin-coated vesicles. |
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Term
Mannose 6-phosphate signal |
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Definition
A phosphate and mannose signal attached to lysosomal proteins in the Golgi. It is recognized by MPRs. |
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Term
Mannose 6-phosphte receptor (MPRs) |
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Definition
Integral proteins in the TGN which recognize lysosomal proteins by their mannose 6-phosphate signals. They bind to GCAs. When the vesicle coat disassembles it returns to the TGN, leaving the lysosomal proteins in the vesicle. |
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Term
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Definition
"Golgi-localizing Gamma-adpatin ear homology domain Arf-bining protein". An adaptor protein in clathrin-coated vesicles which escorts lysosoal enzymes. It binds to Arf1, clathrin and an MPR. |
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Term
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Definition
A protein in clathrin coats. It has a triskelion shape with 3 heavy and 3 light chains. They interact to form a polyhedral lattice. The "hook" in the chain attaches to AP2 adaptors in th membrane. It curves the membrane. When the vesicle disassembles it returns to endosomes or the plant vacuole. |
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Term
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Definition
A G protein which allows veiscles to tether to their specific target membrane. There are over 60 Rabs. In the tethering process two road-shaped proteins (e.g. golgins) form a molecular bridge between the two membranes. |
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Term
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Definition
Tethering proteins in the Golgi body. |
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Term
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Definition
"Soluble Nsf Attachment protein Receptor". Proteins which dock vesicles to their target membrane. There are over 35 different SNAREs, each with specific compartments. They have a SNARE motif. They may be v-SNAREs or t-SNAREs. If you mix v and t-SNAREs in vitro, they fuse with each other but not themselves. After fusion the two SNAREs must be separated using ATP. |
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Term
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Definition
The cytosolic domain of a SNARE. This part interacts with the SNARE's counterpart SNARE (v. vs. t.). |
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Term
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Definition
A SNARE in the vesicle membrane. It's motif binds to the corresponding t-SNARE on its target membrane. There may be more than one SNARE in the complex. |
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Term
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Definition
A SNARE which is in the target membrane. Its SNARE motif binds to the corresponding v-SNARE. There may be more than one SNARE in the complex. |
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Term
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Definition
A bacterial toxin which targets the SNARE complexes of synaptic vesicles, destroying them. This causes paralysis. |
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Term
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Definition
The fusion of a secretory vesicle with the plama membrane, discharging the contents into the extracellular space and delivering membrane proteins to the plasma membrane. Neurotransmitters are emitted this way. SNAP-25, syntaxin, and synaptobrevin are used. |
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Term
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Definition
One of the 2 t-SNAREs used in exocytosis. |
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Term
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Definition
One of the 2 t-SNAREs used in exocytosis. |
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Term
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Definition
The v-SNARE used in exocytosis. |
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Term
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Definition
Guanine Excange Factor. The protein which recruits Sar1 to budding COPII-coated vesicles. |
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Term
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Definition
A three-spindle shape which can form a polyhedral lattice. Clathrin has this shape. |
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Term
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Definition
A molecule which physically links to other molecules together. |
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Term
Very Long Chain Fatty Acids (VLCFAs) |
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Definition
Fatty acids with 24 to 26 carbons. They are oxidized in the peroxisomes. |
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Term
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Definition
Phospholipids with the fatty acids linked to glycerol by ether linkages instead of esther linkages. They are found mostly in myelin sheaths. Abnormalities in them can cause neurological dysfunctions. |
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Term
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Definition
The enzyme which generates the light in fireflies. It is a peroxisomal enzyme. |
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Term
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Definition
H2O2. A highly reactive and toxic substance produced and destroyed in the peroxisomes. It is made by the enzumes urate oxidase, glycolate oxidase, and amino acid oxidase. It is broken up by the enzyme catalase. |
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Term
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Definition
An enzme in very high concentration in the peroxisomes. It breaks up hydrogen peroxide. |
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Term
Alanine/Glyoxylate aminotransferase |
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Definition
An enzme found in the mitochondria of some mammals (cats, dogs), but the peroxisomes of others (rabbits, humans). |
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Term
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Definition
A peroxisome in a plant seedling. The seedling must rely on fatty acids from the seed for energy at first. These organelles convert them to the carbohydrates, generating acetyl CoA which forms citrate which is turned to glucose. |
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Term
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Definition
The scientist from University of Stockholm who in 1962 did a study on a woman who had long-standing fatigue, muscle weakness, elevated metabolic rate, and elevated body temperature. He found that her mitochondria were under no respiratory control. They would make ATP even if there was no ADP. This produced heat rather than chemical work. |
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Term
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Definition
Mainly caused by mutations in mtDNA. They can only be inherited from the mother. Most are characterized by muscle or brain tissue degeneration; both of these tissues produce and require large amounts of ATP. Muscle cells may have abnormal accumulation of mitochondria near the plasma membrane. The mitochondria may be abnormal in size, shape, and structure. The symptoms may be as severe as death in infancy, seizures, blindness, deafness, and stroke-like episodes, or as mild as an intolerance to exercise or non-motile sperm. |
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Term
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Definition
DNA of mitochondria. Circular. Encodes for polypepdides in the IMM, 5% of mitochondria proteins. Mutations cause mitochondrial diseases. It is not protected by a nucleus as in DNA, nor does it have a DNA repair system. It is at risk of being attacked by ROSs. It has a mutation rate 10 times higher than DNA. This is a factor in aging: older people have more mtDNA mutations than younger people. |
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Term
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Definition
When cells contain a mixture of normal and mutant mtDNA. It may vary from organ to organ in the body. Family members inheriting the same disease may show vastly different symptoms and severity. |
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Term
Reactive Oxygen Species (ROS) |
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Definition
A mutagenic oxygen radicle in the electron transport chain. It may cause mutations in mtDNA. |
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Term
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Definition
A neurological disease common in the elderly. It is caused by mutations in mtDNA. Respiratory complex I is damaged. |
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Term
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Definition
A type of illegal synthetic heroin used in the 1980s by drug addicts. It caused the victims to have symptoms similar to Parkinson's Disease. It damaged complex I of the respiratory chain, killing substantia nigra nerve cells. |
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Term
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Definition
A pesticide used on rats. Exposure to it can cause damage to repiratory complex I, creating risk of getting Parkinson's Disease. |
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Term
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Definition
A gene used in experiments on mice. It causes high levels of mtDNA mutation. This causes the mice to age at a very fast rate. They experience hearing loss, graying hair, and osteoporosis. They live to only 1 year. There was no evidence of oxidative damage. Those who were homozygous for the gene aged faster, and those who were heterozygous lived to a normal life span. This proves that mtDNA mutations can cause premature aging, but they are not the cause of natural aging. |
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Term
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Definition
An inherited disease with neurologica, visual, and liver abnormalities. Severe cases can cause death in infancy. |
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Term
Sidney Goldfischer and colleagues |
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Definition
The scientists from Albert Einstein College of Medicine who found that patients with Zellweger Syndrome had only "ghost" peroxisomes in their liver and renal cells. |
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Term
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Definition
A peroxisome which is empty. A membranous sac with no contents. Present in the liver and renal cells of Zellweger Syndrome patients. There are 12 different genes that could be mutated to cause this. |
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Term
X-linked adrenoleukodystroph (X-ALD) |
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Definition
An inherited disease caused by the mutation of the peroxisomal enzyme ABCD1. Lorenzo's Oil was about a boy with this disease. Boys with this disease are unaffected until mid-childhood, when they get the symptoms of adrenal insufficincy and neurological dysfunction. VLCFAs accumulate in the brain, damaging myelin sheaths.
It can be treated with bone marrow transplant, providing normal cells to metabolize VLCFAs. Lovastatin can also be administered to lower VLCFA levels. Gene transplant may be used to cure it. |
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Term
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Definition
A 1993 movie about a boy who suffered from X-ALD. The parents of the boy treat him with a diet increased in certain fatty acids, slowing the process of the disease. Studies found that this diet may not actually be that helpful. |
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Term
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Definition
The peroxisomal membrane protein which is mutated in the disease X-ALD. It normally transports VLCFAs into the peroxisomes to be metabolied. Without it, VLCFAs accumulate in the brain, destroying myelin sheaths. |
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Term
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Definition
A statin which lowers VLCFA and LDL levels. It may be used to treat X-ALD or heart disease. |
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Term
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Definition
The membrane-bound digestive organelle in cells. They are absent in plants. They are diverse in size and structure. They have a role in organelle turnover.
They contain over 50 different hydrolytic enzymes, which are produced in the RER. They can hydrolyze virtually any bological macromolecule. The enzymes are acid hydrolases with low optimum pHs; the pH is around 4.6. This acidity is maintained by V-type H+-ATPase. The interior surface of the organelle's membrane is very glycosylated to protect itself from being digested. |
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Term
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Definition
An enzyme that has an optimal pH level for activity. |
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Term
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Definition
A protein pump in the membrane of the lysosome, endosome, or the tonoplast of the vacuole in plants which maintains the low pH in the organelle. |
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Term
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Definition
Liver cells which engulf aging red blood cells. They have highly irregularily shaped, sized, and coloured lysosomes. |
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Term
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Definition
The cells in mammals which scavenge the body and ingest dead or damaged cells, debris and potentially harmfull micro-organisms. Machrophges, neutrophils. They digest their findings in lysosomes; the low pH kills the micro-organisms. The engulfment of large materials is driven by contractile activities of actin microfilaments.
If an intruder is detected it notifies the immune system via proteins on the plasma membrane. |
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Term
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Definition
Regulated destruction of a cell's own organisms via autophagy. |
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Term
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Definition
"Self eating". The destruction of a cell's own organelles. The organelle is surrounded by a phagophore, producing an autophagosome, which then fuses with a lysosome to form an autolysosome, digesting the organelle and reusing its components. A healthy liver cell will recycle 1 to 1.5% of its proteins every hour. It is slective; only specific organelles are destroyed. It protects the cell from abnormal protein aggregates and invasive bacteria or parasites. It is especially important in brain and nerve cells.
It evolved as a response to nutrient deprivation; it is increased in cells under starvation conditions; energy required for life is taken from the cell itself. This is seen in mammal embryos prior to planting in the uterus wall. |
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Term
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Definition
A double membrane which surrounds worn out organelles and forms an autophagosome during autophagy. They are cup shaped empty vesicles at first, then they surround the organelle and fuse into a double membrane. They may originate from the ER or the mitochondria: it is unclear which. |
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Term
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Definition
A worn out organelle surrounded by a phagophore. It fuses with a lysosome to form an autolysosome. |
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Term
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Definition
An autophagosome which has fused with a lysosome. The inner layer of the autophagosome as well as organelle within it is then digested by the lysosomal enzymes. After digestion it becomes a residual body. |
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Term
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Definition
Genes required for autophagy. If they are missing or deleted it can cause development and physiology problems. |
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Term
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Definition
An autolysosome after digestion of the contents is complete. The contents may be eliminated by exocytosis or it could become a lipofuscin granule, depending on cell type. |
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Term
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Definition
Residual bodies that are not eliminated by exocytosis. Instead it stays in the cell. They accumulate over time. Older cells have more; they are a part of the aging process. |
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Term
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Definition
A plant metabolic by-product which is dumped for good into the vacuole. |
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Term
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Definition
The membrane that binds the vacuole of plant cells. It has active transport proteins that pump in ions. Water then fills the vacuole by osmosis, puffing it up and giving the cell mechanical support from turgor pressure.
It has a network of tubules on its outer side which act as fusion platforms. |
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Term
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Definition
When the plasma membrane receptors bind to specific ligands and then the membrane invaginates, forming a vesicle. There are two types: bulk-phase/pinocytosis, or receptor-mediated. |
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Term
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Definition
"Cell eating". When a cell internalizes fluid from the extracellular space, perhaps along with a large particle. Many single-celled organisms eat this way. Animals use it for protection. |
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Term
Bulk-phase endocytosis/Pinocytosis |
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Definition
A form of endocytosis. The uptake of non-specific fluids from the extracellular space along with a section of plasma membrane. There may be particles present in the fluid, which gain access to the cell. You can visualize this by putting a cell in a dyed fluid. |
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Term
Receptor-Mediated Endocytosis (RME) |
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Definition
A type of endocytosis. Specific ligands in the extracellular space are recognized and taken up by receptors, along with a section of the plasma membrane. This allows cells to take up materials that may be in low concentration (hormones, growth factors, enzymes). |
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Term
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Definition
A specific molecule in the extracellular space which is recognized and picked up by receptor proteins during RME. |
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Term
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Definition
The indent in the plasma membrane that is formed during clathrin-mediated RME. Its surface has 10 to 20 times the concentration of protein receptors than other regions of the plasma membrane. The cytoplasmic side appears bristly and dark. |
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Term
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Definition
The adaptors in clathrin-coated vesicles. It is recruited to the plasma membrane by PI(4,5)P2. The clathrin "hooks" bind to it at the vertices of the polygon that is forming. It can bind to a diverse array of accessory proteins. It is 4 polypeptide subunits, including the μ subunit and β subunit. |
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Term
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Definition
The lipid-anchored protein in high concentration on the cytosolic leaflet of the plasma membrane which recruits AP2 adaptors for clathrin-coated vesicle formation. It is rapidly created and destroyed by enzymes, thus regulating endocytosis. |
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Term
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Definition
The subunit of AP2 adaptor which attaches to the cytoplasmic tails of specific ligand receptors, determining what ligands will be recruited. |
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Term
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Definition
The AP2 adaptor subunit which attaches to clathrin. |
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Term
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Definition
Proteins involved with cargo recruitment, vesicle release, cytoskeletal interaction, coat uncoating, and vesicle docking during vesicle transport. E.g. dynamin. |
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Term
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Definition
An accessory protein in the formation of clathrin-coted vesicles. It is a G protein required for the release of the vesicle from its donor membrane. It forms a helical collar around the neck of the coated pit. When it is hydrolyzed to GDP form there is a twisting motion, pinching off the vesicle. |
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Term
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Definition
An accessory protein in clathrin-coated vesicles which dissociates the clathrin coat from the vesicle after it is fully formed. |
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Term
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Definition
A phospholipid. It has 7 different types based on where the phosphate group is added on the sugar ring: PI(3)P, PI(4)P, PI(5)P, PI(3,4)P2, PI(4,5)P2, PI(3,5)P2, and PI(3,4,5)P3. These are recognized by proteins, giving the membrane an identity, playing a role in endocytosis.
PI(3)P means early endosomes. PI(3,5)P2 means late endosomes. PI(4)P means the TGN and secretory granules/vesicles. |
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Term
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Definition
A receptor that uptakes materials that will be used by the cell, such as transferrin or LDL. When it reaches the early endosome, its ligand detaches due to the pH. It then concentrates in specific tubular combartments and is returned to the plasma membrane by budding vesicles. |
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Term
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Definition
Receptors wchich uptake ligands that carry messages and change activities in the cell. They bind to insuling, hormones, or growth factors such as EGF and trigger physiologic responses in the cell. The receptor is destroyed in receptor-down regulation.
When inside the endosome, it is bound into small vesicles inside its lumen by ESCRT complexes. |
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Term
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Definition
The detruction of a signaling receptor after it has carried its message. This reduces the cell's sensitivity to further stimulation by the ligand. The receptor is marked with ubiquitin for endocytosis and destruction. |
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Term
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Definition
The protein which binds to other proteins, such as used signal receptors, signaling for it to be destroyed. It attaches to incorrectly formed, folded, or associated proteins. They attach using the enzymes E1,E2, and E3. They form chains covalently linked to each other. It attaches to a lysine residue with the enzyme ubiquitin ligase. They then bind to the cap of a proteasome and string the protein through. |
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Term
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Definition
A network of vesicles and tubules to which imported materials are transported. They are the distribution centers in th endocytic pathway. The lumen is acidifie by an H+-ATPase. There are two types: early and late. |
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Term
Late endosome/Multivesicular Bodies (MVB) |
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Definition
Endosomes closer to the nucleus. They form from early endosomes. They have a lower pH than early endosomes, and contain Rab5. It has ligands from the early endosomes which it transports to the lysosomes. Signaling receptors bound to ubiquitin tags are put into in small vesicles inside the lumen of this organelle. |
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Term
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Definition
Where receptors and their ligands are first taken in the endocytic pathway.It matures into a late endosome. They have a higher pH than late endosomes and they have Rab7.
Housekeeping receptors then release their ligands due to the pH; they are then stored in specific tubules before being returned to theplasma membrane by budding vesicles. The ligands move on to the late endosome. |
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Term
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Definition
A protein complex which packages used signaling receptors into vesicles inside the lumen of the endosome. They sort ubiquinated receptors into a cluster, cause the cluster to invaginate into the late endosome, and sever the neck, releasing the vesicle. |
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Term
Low-Density Lipoprotein (LDL) |
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Definition
A particle with a central core of around 1500 cholesterol molecules esterfied into long-chain fatty acids. It is coated by a single phospholipid layer and a single protein apolipoprotein B-100. It delivers cholesterol from the liver to other cells via the bloodstream. |
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Term
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Definition
The protein attached to LDLs. It binds to LDL receptors, a housekeeping receptor that forms coated pits. The LDL enters the endocytic pathway and its protein is degraded and the cholesterol de-esterfied and made into membrane or steroid hormones. |
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Term
Niemann-Pick type C diasese |
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Definition
A disease where the protein which transfers cholesterol out of the lysosomes after an LDL is taken up is missing. Cholesterol builds up in lysosomes, causing nerve degeneration and early childhood death. |
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Term
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Definition
A disease where plaques form in the inner lining of arteries, reducing blood flow and forming blood clots which cause heart attack. Free radicles change LDLs, which then injure the endothelial cells, which inflame, forming a plaque of macrophage foam cells. The disease is caused by chronic inflammation. |
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Term
Myocardial infarction/Heart attack |
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Definition
Caused by blood clots in the arteries, which are caused by atherosclerosis. |
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Term
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Definition
The cells which form a plaque in atherosclerosis. Macrophages and white blood cells attempt to help the situation by ingesting the damaged LDLs. They become filled with cholesterol-rich fatty droplets. A fibrous cap forms over them, bulging into the artery, reducing blood flow. Rupture of the plaque causes blood clotting and heart attack. |
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Term
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Definition
A drug which lowers the LDL levels in the blood. They are used to treat high risk of heart attack. E.g lovastatin, lipitor. They block HMG CoA reductase. |
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Term
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Definition
A key enzyme in cholesterol synthesis. Statins block its activity, reducing LDL levels in the blood. |
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Term
High-Density Lipoproteins (HDL) |
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Definition
"The good cholesterol". Similar in structure to LDLs, but their protein is apolipoprotein A-I. They deliver excess cholesterol from the plasma membrane of cells to the liver for excretion, reducing risk of heart attack. The benefits of high HDl is not clear-cut. |
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Term
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Definition
The protein in HDL particles. |
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Term
Cholesteryl Ester Transfer Protein (CETP) |
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Definition
An enyme which transfers cholesterol from HDL to other lipoprotein particles, lowering HDL levels. Some families in Japan have a mutation for this enzyme and they live to be over 100 years old. |
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Term
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Definition
A CETP inhibitor which increases HDL levels, but if taken with a statin, causes patients to be much more likely to die. |
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Term
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Definition
A CETP inhibitor which increases HDL levels by over 100%. It remains to be seen if it can lead to long-term survival of heart attack risk patients. |
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Term
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Definition
An enzyme which destroys LDL receptors in the liver. Without it, you have reduced LDL levels and decreased heart disease. They are developing inhibitors for it. |
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Term
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Definition
The vesicle that forms after phagocytosis. It contains the uptaken particle(s) and fluid. It fuses with a lysosome, forming a phagolysosome. |
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Term
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Definition
A phagosome after it has fused with a lysosome. The food particle(s) within are digested. |
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Term
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Definition
A disease caused by myobacterium tuberculosis. The bacteria is engulfed by a phagocyte, it is taken into the cytoplasm via phagocytosis, but it inhibits being fused with a lysosome, and resists high pH. |
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Term
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Definition
Caused by Coxiella burnetii which is taken into the phagocyte by phagocytosis, but resists the high pH in the phagolysosome. |
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Term
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Definition
Caused by Listria monocytogenes, which is taken into the phagocyte by phagocytosis, but it destroyes the phagolysosomal membrane and escapes into the cytoplasm. |
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Term
Avram Hershko, Aaron Ciechanoer, Irwin Rose, and Alexander Varshavsky |
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Definition
The scientists who in the 1970s to 1980s discovered proteasomes and won the Nobel Prize in 2004. |
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Term
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Definition
The rings in proteasomes which are the proteolytic enzymes. Their active sites face the inside of the barrel. It has 3 subunits that are active. |
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Term
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Definition
The enzyme which attaches ubiquitin to a lysine residue on a condemnd protein. Different kinds of this enzyme recognize different proteins and their different destruction signals. |
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Term
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Definition
A drug which inhibits proteasome action, treating some forms of cancer. |
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Term
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Definition
A protein sequence which ensures the protein won't stay for long in the cell. |
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Term
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Definition
The pressure that a plant vacuole gives against the other parts of the cell, giving the cell mechanical support |
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Term
Apoptosis/Programmed Cell Death (PCD) |
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Definition
A series of events that kills a cell. The volume decreases, it lose adhesion to neighbor cells, the surface wrinkles, chromtin is broken up, increased phagocytosis. This eliminates damaged cells, used in embryo development. Capsases and proteases cleave essential proteins. It can be extrinsic or intrinsic pathways. |
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Term
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Definition
External factors such as ionizing radiation, elevated temperature, or toxins cause the cell death. |
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Term
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Definition
Internal factors such as hypoxia, Ca2+, or ROS cause apoptosis. Cytochrome C is released, the cell condenses into apoptic bodies which are taken up by macrophages. |
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Term
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Definition
Smaller condensed contents of a cell bound in membrane after the PCD. They are taken up by macrophages. This way none of the cytosol ends up in the extracellular environment. |
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Term
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Definition
A tubule which extends from a peroxisome when the cell senses stress. Extension is rapid and transient. It can be elicited by intense light and hydrogen peroxide. This is a normal phenomenon in plant cells. |
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Term
Outer Mitochondrial Membrane (OMM) |
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Definition
The outer membrane of the mitochondria. Contains the intermembrane space and IMM. |
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Term
Inner Mitochondrial Membrane (IMM) |
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Definition
The inner membrane of a mitochondria. Contians the matrix. Has a 3:1 protein/lipid ratio. It has cristae and is highly impermeabe. Rich in the phospholipid cardiolipin. Contains the machinery for aerobic respiration and ATP formation. |
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Term
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Definition
Folds in the IMM which increase surface area. |
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Term
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Definition
The space between the OMM and IMM of a mitochondria. The proteins here have a major role in apoptosis. |
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Term
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Definition
The lumen of the IMM in a mitochondria. It has a negative charge. It has a high protein concentration and a gel-like consistency. Mitochondrial ribosomes and mtDNA dwell here. |
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Term
Post-translational protein import |
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Definition
When a protein is imported after it is fully created by ribosomes in the cytosol. Includes import to nucleus, peroxisomes, mitochondria, and chloroplasts. Except for peroxisomes, the protein is unfolded when it enters. |
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Term
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Definition
A removable target sequence at the N-terminus of a protein which directs it to the matrix. It has a positive charge. |
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Term
Translocase of Outer Membrane (TOM) complex |
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Definition
A pore shaped complex in the OMM which recognizes and allows diffusion of proteins through or into the OMM. It has receptors and a protein lined channel. It occurs close to a TIM complex so that proteins can pass through both directly. |
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Term
Translocase of the Inner Membrane (TIM) complex |
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Definition
A pore shaped complex in the IMM which recognizes and allows diffusion of proteins through or into the IMM. It occurs close to a TOM complex so proteins can pass through both directly. Includes TIM22 and TIM23. |
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Term
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Definition
A TIM complex which imports integral proteins into the IMM. |
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Term
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Definition
A TIM complex which imports proteins into the matrix. It is driven by the fact that the matrix is negative and the presequence is positive. Import involves biased diffusion. Once inside the matrix, the presequence is removed and the protein is fully folded. |
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Term
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Definition
A reaction where electrons are lost. |
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Term
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Definition
A reaction where electrons are gained. |
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Term
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Definition
"Sugar splitting". The first stage in the catabolism of glucose. Occurs in the cytosol. 6 carbon glucose splits into two 3 carbon pyruvates and NADH. Occurs without using oxygen. A 10 step process. All steps are at equilibrium except steps 1, 3, and 10, which use hexokinase, phosphofructokinase, and pyruvate kinase, respectively. 2 ATP must be invested; the sugar is phosphorylated. |
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Term
Tricarboxylic acid (TCA)/Citric acid/Krebs cycle |
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Definition
The second step in the catabolism of glucose. Discovered by Hans Krebs. Occurs in the matrix of the mitochondria in eukaryotic cells and the cytosol of prokaryotes. Releases the majority of energy in glucose. Carbon is oxidized into carbon dioxide. Electrons are transfered onto electron carriers. All energy-providing molecules can be broken into metabolites of this cycle. Acetyl CoA enters the cycle and turns into OAA, then citrate. 2 carbons are removed from citrate, forming CO2 and OAA. One FADH2 and three NADH are produced each cycle. |
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Term
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Definition
Nicotinamide Adenine Dinucleotide Hydrogen. A high energy metabolite created from NAD+ in glycolysis and the TCA cycle. It transfers its high-energy electrons into the electron transport chain. NADH formed in glycolysis enters the mitochondria using either malate-asparate shuttle or glycerol phosphat shuttle. |
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Term
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Definition
A 3 carbon molecule formed by splitting glucose (a 6 carbon molecule) in half during glycolysis. It enters the mitochondria and is decarboxylated into a 2 carbon acetyl group which then attaches to coenzyme A, becoming acetyl CoA. |
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Term
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Definition
A complex organic molecule which attaches to the 2 carbon acetyl group that forms from pyruvate in the mitochondria. This reaction is facilitated by pyruvate dehydrogenase. It then beceomes acetyl CoA. It is derived from pantothenic acid. |
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Term
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Definition
Coenzyme A attached to an acetyl group. Created from pyruvate, making NADH. Can be from the fatty acid cycle, or amino acid breakdown. It then enters the TCA cycle. |
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Term
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Definition
A high-energy molecule formed from FADH+ in the TCA cycle. It transfers its high-energy electrons into the electron transport chain. |
|
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Term
Oxidative Phosphorylation |
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Definition
The production of ATP in the mitochondria. A proton gradient is formed by the electron transport chain, which then powers ATP synthase. |
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Term
Electron Transport Chain (ETC) |
|
Definition
A series of electron transporters in the IMM. Complexes I (NADH dehydrogenase), II (succinate dehydrogenase), III (cytochrome bc1), and IV (cytochrome c oxidase), as well as 2 other carriers. Electrons are added to it by FADH2 and NADH. Electrons are passed down, coupling energy releasing reactions with energy requiring reactions, creating a proton gradient in the intermembrane space, the electron losing a little energy every time. When all the energy is used up, it passes to oxygen, becoming water. |
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Term
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Definition
A complex which phosphorylates ADP into ATP using the proton gradient in the intermembrane space of the mitochondria. Potential energy in the proton gradient becomes the energy of the ATP. |
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Term
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Definition
The process of turning energy-containing molecules into ATP, using oxygen and forming carbon dioxide and water. Done with glycolysis, the TCA cycle, and oxidative phosphorylation. The opposite of photosynthesis. |
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Term
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Definition
The ability of a cell or cell structure to change shape, size, and structure. |
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Term
|
Definition
A reactive molecule. Dynamic and free-moving in the body. Can cause harm to the cell. The cause of many illnesses. |
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Term
|
Definition
A sugar or sugar polymer. Their energy is stored in the H-C-OH units. |
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Term
|
Definition
A molecule with fatty acids. The energy is stored in their H-C-H units. Stores more energy than carbohydrates. |
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Term
Arthur Harden and William Young |
|
Definition
British chemists who in 1905 studie the breakdown of glucose in yeast. Saw that CO2 bubbles stopped if there was no inorganic phosphates, even if there was adequate glucose. |
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Term
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Definition
When oxygen is absent, after glycolysis (which requires no oxygen) NADH oxidies pyruvate, making lactate. |
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Term
|
Definition
Formed from oxidized pyruvate in fermentation after glycolysis. |
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Term
Substrate-level phosphorylation |
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Definition
The process in glycolysis where the sugar is initially phosphorylated, releasing some energy. 2 ATP are required, one at a time they phosphorylate the glucose. After this it splits into two 3 carbon monophsophates, which each produce a NADH and ATP, turning into pyruvate. |
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Term
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Definition
Vitamin B2. Coenzyme A is derived from this vitamin. |
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Term
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Definition
The enzyme which facilitates the attachment of CoA to pyruvate minus one carbon, forming acetyl CoA |
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Term
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Definition
The British biochemist who in the 1930s discovered the TCA cycle. He wrote about it to Nature journal, but they rejected it, so he published it in a different journal. |
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Term
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Definition
A 4 carbon metabolite of the TCA cycle. It is formed by removing carbons from citrate. It is combined with acetyl CoA to make citrate. |
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Term
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Definition
A 6 carbon metabolite of the TCA cycle. It is formed by combining OAA with acetyl CoA. 2 of its carbons are removed and turned into carbon dioxide, turning it into OAA. |
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Term
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Definition
CO2. Formed in the TCA cycle when two carbons are removed from citrate. |
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Term
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Definition
Fatty acids are broken down into 2 carbon acetyl CoAs, which can enter the TCA cycle. |
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Term
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Definition
A shuttle which carries the electrons from NADH produced by glycolysis (in the cytosol) into the mitochondrion. Once inside, it reduces a NAD+. |
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Term
Glycerol phosphate shuttle |
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Definition
A shuttle which carries the electrons of NADH formed by glycolysis (in the cytosol) into the mitochondria. NADH reduces DHAP, which is shuttled into the mitochondrion where it reduces FAD. |
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Term
Dihydroxyacetone phosphate (DHAP) |
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Definition
A molecule which is reduced by NADH produced by glycolysis (in the cytosol). It is shuttled into the mitochondrion by a glycerol phosphate shuttle, where it reduces a FAD. |
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Term
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Definition
The scientist from the Univeristy of Edinburgh who in 1961 proposed the idea of chemiosmotic mechanism of ATP synthesis. |
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Term
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Definition
The mechanism by which the mitochondria produces ATP. The electron transport chain produces a proton gradient, which then powers ATP synthase, making ATP. Every 2 electrons produces about 3 ATP. |
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Term
Peroxisomal Targeting Signal (PTS) |
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Definition
A signaling sequence that causes proteins to be delivered to the peroxisome. PTS delivers to the matrix, mPTS delivers to the peroxisome membrane. Recognized by PTS receptors. |
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Term
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Definition
Receptors that bind to PTSs in the cytosol and shuttle them to the peroxisome. |
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Term
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Definition
A PTS receptor that creates a large pore in the peroxisome. |
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Term
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Definition
A chaperone in the mitochondria matrix which helps the protein to fold correctly, and removes its presequence. |
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Term
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Definition
When proteins can diffuse in, but can't diffuse out. Occurs in the mitochondria matrix. |
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Term
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Definition
A chaperone in the mitochondria matrix which may either aid in the diffusion of proteins into the matrix, or physically pull the proteins in, using ATP. It acts as a Brownian ratchet. |
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Term
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Definition
A mechanism which aids in biased diffusion. Brownian = random diffusion. Ratchet = only allowed in one direction. |
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Term
Translocon of Outer Chloroplast membrane (TOC) complex |
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Definition
The complex that imports proteins to or through the outer membrane of a chloroplast. |
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Term
Translocon of Inner Chloroplast membrane (TIC) complex. |
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Definition
The complex that imports proteins into or through the inner membrane of a chloroplast. |
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Term
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Definition
A sequence on thhe N terminus of proteins being imported to the chloroplast. It varies in length and sequence, directing it to the correct sub-compartment in the chloroplast. |
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Term
Stroma targeting domain (STD) |
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Definition
The portion of the targeting peptide which directs it to the stroma. Present in proteins being imported to the stroma or thylakoid. If it is destined for the thylakoid, the STD is removed, revealing TTD. |
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Term
Thylakoid transfer domain (TTD) |
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Definition
The portion of the transit peptide which directs the protein to the thylakoid. The protein then enters the thylakoid in a way similar to how a protein enters a cyanobacteria. Many thylakoid membrane proteins are imported cotranslationally by choroplast ribosomes. |
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Term
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Definition
An organim which is a heterotroph in the dark and an autotroph when there is light. |
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Term
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Definition
The coral provides CO2 to algae, which turn it into carbohydrates and fats using sunlight. The coral then feeds on these. It is composed of the dead skeletons of coral algae. If the water around the coral is bad, the algae die and the coral turns a bleached colour. |
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Term
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Definition
A sea slug that feeds on algae and retains the choroplasts, making it able to photosynthesize. |
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Term
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Definition
Flattened membrane sacs found in the stroma of a chloroplast. This is where the photosynthetic machinery is. They may form grana or be alone in the stroma. The membrane is very fluid. It contains chlorophyll which stores solar energy in ATP and NADPH. |
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Term
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Definition
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Term
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Definition
The space between the thylakoid and the inner membrane in a chloroplast. It contains proteins. Carbohydrate synthesis occurs here. |
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Term
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Definition
A pigment found in the thylakoid membrane. It contains magnesium. It is a light absorbing pigment. It absorbs violet-blue and red light, reflecting green. They group togeher, forming a photosynthetic unit. |
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Term
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Definition
A pigment found in thylakoids which absorbs green light, reflecting red, orange, yellow, et cetera. |
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Term
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Definition
A cluster of chlorophylls, with a reaction centre in the middle. Found in the membrane of the thylakoid. It harvests light of various wavelengths and transfers the energy to the reaction center. |
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Term
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Definition
An arm-like extension of a plastid. It may extend, branch, and create polygonal shapes. It extends between ER-lined channels. This interaction is responsible for the flow of metabolites, lipids, and vitamins. |
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Term
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Definition
A plastid which contains starch. |
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Term
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Definition
A plastid which is a colour other than green or white. |
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Term
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Definition
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Term
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Definition
A choloroplast without any chlorophyll. Occurs when the plant become etiolated in the dark. The plant goes pale. |
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Term
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Definition
A plastid which is used to sense gravity. |
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Term
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Definition
The scientist from Stanford University who in 1931 proposed that during photosynthesis the oxygen released was derived from water rather than carbon dioxide, as previously believed. He developed this theory by comparing the chemical equations of sulfur bacteria with the equation for photosynthesis.
CO2 + 2H2S --> (CH2O) + O2
CO2 + 2H2O --> (CH2O) + 2S |
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Term
Samuel Ruben and Martin Kamen |
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Definition
The scientists from the University of California who in 1941 proved van Niel's theory that photosynthesis derived the oxygen it released from water and not carbon dioxide. They did this by giving one plant isotope labelled water and one plant isotope labelled carbon dioxide. The plant with labelled water gave off labelled oxygen, and not the plant with labelled carbon dioxide. |
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Term
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Definition
The reactions in photosynthesis that require light to work. Energy is absorbed and stored in NADPH and ATP. |
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Term
Light-independent/Dark reactions |
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Definition
Reactions in photosynthesis that do not require light, and could work in the dark. Energy stored in NADPH and ATP is converted into sugars, using CO2. |
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Term
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Definition
The membrane surrounding the nucleus. It has nuclear lamina and nuclear pores. It is a double membrane. The outer membrane binds ribosomes, and it is continuous with the RER. The inner membrane contains integral proteins that connect to nuclear lamina. The two membranes are 10 to 50 nm apart. The intervening space is continuous with the ER. |
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Term
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Definition
A thin meshwork of filaments bound to the inner membrane of the nuclear envelope via integral membrane proteins. It gives support to the nuclear envelope and is an attachment site for chromatin. |
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Term
Hitchinson-Gilford Progeria Syndrome |
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Definition
A rare disease caused by mutations in the lamina gene LMNA. Causes premature aging in children. |
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Term
Nuclear Pore Complex (NPC) |
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Definition
A hole that goes through both layers of the nuclear envelope, fusing the two layers together. Each nucleus has 3 to 4 thousand pores. The pore is 9 nm in diameter. It imports proteins from the cytosol. These proteins are essential to nucleus functions. Small proteins can diffuse freely in and out. Larger proteins must have an NLS.
It is a protein complex with hundreds of polypeptides. It has oxtagonal symmetry. It has cytoplasmic filaments and a nuclear basket. |
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Term
Nuclear Localization Signal (NLS) |
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Definition
A signal sequence which directs a protein to the nucleus and allows it to pass through th NPC. It is positively charged and on the C-terminus. |
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Term
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Definition
RAs related Nuclear protein. A G protein. It interacts with importins, causing them to release their cargo when in the nucleus. |
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Term
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Definition
Importins and exportins. Bind to cargo when passing through the NPC. |
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Term
Nuclear Export Signal (NES) |
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Definition
A signal sequence that causes a protein or RNA to be exported from the nucleus. |
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Term
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Definition
A structure inside a nucleus. There may be more than one per nucleus. It is surrounded by DNA and is produces ribosomes and rRNA. Ribosomes are exported to the cytoplasm in separte pieces, 40S and 60S. It has a dense fibrillar component, a fibrillar center, and a granular component. |
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Term
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Definition
The region of the nucleolus which contains ribosome subunits in various stages of assembly. |
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Term
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Definition
The region of the nucleolus which contains DNA encoding for ribosomal RNA. |
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Term
Dense fibrillar component (dfc) |
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Definition
The region of the nucleolus which contains nascent pre-rRNA transcripts and proteins. |
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Term
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Definition
The man who discovered the nucleus. He didn't publish his findings because he feared prosecution. Also he didn't know what they did exactly. |
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Term
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Definition
Chromatin that is not dispersed in the nucleus. Not replicated easily. Not often transcribed or replicated. |
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Term
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Definition
Chromatin that is often being transcribed and translated. |
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Term
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Definition
A dynmic network of protein filaments that gives structural support and a transport system for organelles and vesicles. Provides contractility and motility and spacial organization. Formed from microtubules, intermeidate filments, and microfilaments. |
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Term
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Definition
The largest cytoskeletal elment; 25 nm in diameter. Made from α-tubulin and β-tubulin, which form protofilaments that form long hollow cylinder. It has a fast-growing "plus" end and a slow-growing "minus" end. It has structural polarity. It has dynamic instability; a half-life of just minutes. |
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Term
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Definition
A microtubule-associted motor protein that powers incracellular transport towards the minus end of a microtubule. Uses ATP to move material along the microtubule or generate sliding between microtubules. |
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Term
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Definition
A microtubule associated motor protein which powers intracellular transport towards the plus end of a microtubule. Uses ATP to move materials along the microtubule or generate a sliding force between microtubules. |
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Term
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Definition
When the plus end of a microtubule shrinks rapidly. |
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Term
MicroTubule-Organizing Centre (MTOC) |
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Definition
The central cite of microtubule assembly. During mitosis the mitotic spindle forms from it. The MTOC is split into two centrosomes. |
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Term
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Definition
The central major site of microtubule organization in animal cells. Made from two centrioles. |
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Term
Intermediate Filaments (IF) |
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Definition
The medium sized component of the cytoskeleton; 10 to 12 nm in diameter. Only found in multicellular animals. Provides mechanical strength and support. Very stable relative to microtubules or microfilaments. Formed from fibrous proteins containing an α-helical domain. There are keratins, neurofilaments, and lamins.
Polar proteins with N and C termini. Conglomerate in a staggered way for maximum strength. Attach to each other anti-parallel, so there is no polarity in the end structure.
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Term
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Definition
The smallest cytoskeleton element; 8 nm in diameter. Made from the protein actin. Provides maintenance of cell shape, cell movement, cytokinesis, and muscle contractions. |
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Term
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Definition
The protein that microtubules are made out of. It has two forms, filamentous (F) and globular (G). F-actin is polar and arranges itself anti-parallel. |
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Term
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Definition
Proteins that control F-actin filaments. Used to create microtubule monomers, sequester monomers, cap filaments, cross-link filaments, budle filaments, bind filaments to membrane, or depolymerize. |
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Term
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Definition
An F-actin associated motor protein. It is a large family of proteins. They move towards the plus end of the microfilament. There are conventional and unconventional myosins. The unconventional generate force in non-muscle cells. |
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Term
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Definition
The space outside of the cell. Contains secreted materials, materials that influence cell behaviour. |
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Term
Extra-Cellular Matrix (ECM) |
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Definition
An organized network of material produced and secreted by the cell. Mediates cell-to-cell interactions, provides mechanical protection, serves as a barrier, and binds regulatory factors. Include the cell wall of plants and fungi. |
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Term
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Definition
An ECM found in plants. Composed of cellulose, hemicellulose, pectin, and proteins. Provides support for the cell, protects it from damage and pathogens, and contains biochemical information for the cell. |
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Term
Microtubule Associated Proteins (MAPs) |
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Definition
Proteins such as motor proteins dynein and kinesin which are associated with the microtubules. |
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Term
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Definition
The monomer which DNA is made from. Each consists of a phosphate group, a five-carbon sugar (2-deoxyribose in DNA, ribose in RNA), and one of the four cyclic nitrogenous bases, a purine or a pyrimidine. They form phosphodiester bonds with each other. |
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Term
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Definition
The bond between two nucleotides |
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Term
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Definition
The end of a strand of DNA (there are 2 strands per DNA) that has a free phosphate group. It associates with the 3' end of the other strand. |
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Term
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Definition
The end of a strand of DNA (there are two strands per DNA) that has a free hydroxyl group. It associates with the 5' end of the other strand. |
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Term
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Definition
A pyrimidine. It pairs with adenine forming 2 hydrogen bonds (weaker than a C-G bond). It is found only in DNA. In RNA it is replaced by uracil. Its common form is keto. Its rare form is enol. |
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Term
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Definition
A purine. It pairs with thymine forming 2 hydrogen bonds (weaker than a C-G bond). Its common form is amino. Its rare form is imino. |
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Term
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Definition
A pyrimidine. It pairs with guanine forming 3 hydrogen bonds (stronger than an A-T bond). Its common form is amino. Its rare form is imino. |
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Term
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Definition
A purine. It pairs with cytosine forning 3 hydrogen bonds (stronger than an A-T bond). Its common form is keto. Its rare form is enol. |
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Term
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Definition
A nucleotide with a nitrogenous base that has a single sugar ring. Thymine and cytosine. |
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Term
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Definition
A nucleotide that has two sugar rings in its nitrogenous base. Adenine and guanine. |
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Term
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Definition
The most common form of DNA. Found in living organisms. DNA takes this form in aqueous solutions with low concentration salts. It is right-handed. It has a major and minor grove. Substrates are every 0.34 nm, with 10 base pairs per 360 degree turn. It is 1.9 nm thick. |
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Term
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Definition
In living cells DNA is tightly coiled. Coils can be positive or negative. In eukaryotes first the DNA wraps into nucleosomes, then it coils into a 30 nm fibre in one of three ways: solenoid, expanded, or contracted (not sure which one is true). The 30 nm fibre then folds into a mitotic chromosome using a scaffold. |
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Term
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Definition
Proteins and nucleic acids. In prokaryotes the DNA is circular. Humans have 23 chromosomes. Other species have different numbers. In mitotic phase they are supercoiled and they are visible with a light microscope, but during interphase they are impossible to distinguish from. |
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Term
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Definition
The first level of supercoiling in eukaryotic cells. A octamer of histone proteins with tails, two each of H2a, H2b, H3, and H4. DNA wraps around one almost twice, 146 nucleotides, producing a 11 nm diameter fibre. The histones have tails that protrude and are exposed to enzymes, which controls gene expression. Another histone, H1, clamps the DNA into place. This forms a structure like a string of beads. The linker region is 8 to 114 nucleotides long. |
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Term
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Definition
The region of DNA between two nucleosomes. It is susceptible to digestion by nucleotides. When this happens, discretely sized segment are produced. |
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Term
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Definition
Sometimes genes don't matter. The conditions that the organismis raised in determine the phenotypes of the organism. Not nature vs. nurture, nature and nurture. |
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Term
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Definition
The DNA found in chloroplasts. Circular. It is longer than mtDNA. |
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Term
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Definition
The histone that clamps shut a nucleosome, making it really hard for DNA to spontaneously unwrap. |
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Term
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Definition
One of the two models for how nucleosome strands curl into 30nm chromatin fibres. They pack into a curl with 6 nucleosomes per turn. This is observed under a light microscope. |
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Term
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Definition
One of the two models for how nucleosome strands curl into 30nm chromatin fibres. It packs into a zigzag formation of various densities. This is observed after cryopreservation of a sample (quick freezing). |
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Term
Heinz Fraenkel-Conrat and colleagues |
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Definition
In 1957 they did an experiment on tobacco mosaic virus. They separated the protein from the RNA and proved that it is RNA, not protein that carries genetic information. |
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Term
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Definition
The five-carbon sugar found in DNA. |
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Term
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Definition
The five-carbon sugar found in RNA. |
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Term
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Definition
A single nucleic acid strand. Some viruses use only RNA. In the place of thymine, it has uracil. Not as stable as DNA. In the past, it was called a naked molecule of DNA. This is because they don't have associated proteins or complex morphology. In reality, RNA are different in chemical structure than DNA. |
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Term
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Definition
A pyrimidine. It pairs with adenine forming 2 hydrogen bonds (weaker than a C-G bond). It is found only in RNA. In DNA it is replaced by thymine. |
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Term
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Definition
A macromolecule that consists of nucleotide subunits. DNA and RNA. It has genotypic (replicatioin), phenotypic (gene expression), and evolutionary (mutation) functions. |
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Term
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Definition
Keep the backbones of DNA curled into a helix when in an aqueous solution. |
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Term
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Definition
Describes the way that the 5' end is paired with the 3' end of each strand and vice versa in a DNA molecule. |
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Term
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Definition
Describes how both the strands in DNA have the exactly correct nucleic base sequence so that they can join each other to form DNA. This is what makes DNA such a great molecule for storing and transmitting genetic information. |
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Term
James Watson and Francis Crick |
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Definition
Deduced the structure of DNA in 1953 using the findings of Erwin Chargaff and colleagues, Maurice Wilkins, and Rosalind Franklin. They, along with Wilkins, won the Nobel Prize in 1962. |
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Term
Erwin Chargaff and colleagues |
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Definition
Found that the concentration of purines is always equal to the concentration of pyrimidines in DNA so that A = T and C = G. |
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Term
Maurice Wilkins and Rosalind Franklin |
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Definition
Used the X-ray diffraction patterns of DNA to provide crucial evidence that Watson and Crick used to deduce the structure of DNA. Wilkins won the Nobel Prize in 1962, but Franklin died before that. |
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Term
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Definition
The form DNA takes in a high concentration salt solution. It is right-handed with 11 nucleotides per 360 degree turn. It is 2.3 nm in diameter. Occurs almost never in vivo. |
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Term
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Definition
A form of DNA that is left-handed with 12 nucleotides per 360 degree turn. It is 1.8 nm in diameter. It is C-G rich. Its function in living things is unclear. |
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Term
Positive supercoil/overwound DNA |
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Definition
Right-handed supercoiling. Some archaebacteria have positively supercoiled DNA. |
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Term
Negative supercoil/underwound DNA |
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Definition
Left-handed supercoiling. Almost all organisms have negative supercoiling. |
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Term
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Definition
Having only one set of genes. Not to be confused with haploid. Prokaryotes are monoploid. |
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Term
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Definition
Having one set of chromosomes. Not to be confused with monoploid. Gametes are haploid. |
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Term
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Definition
A virus that uses RNA. The smallest ones have 3 genes. |
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Term
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Definition
A virus that uses DNA. The smallest have 9 to 11 genes and the largest around 150 genes. |
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Term
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Definition
The state of a circular DNA (such as in prokaryotes) when it is supercoiled. If you cleave the DNA at certain sites or destroy its associated RNA and protein connectors, the loops relax, causing "nicks", unfolded regions. |
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Term
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Definition
Having two complete sets of genes, one from each parent. Most eukaryotes are diploid. They form from the fertilization of two haploid gametes together. |
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Term
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Definition
Having more than 2 copie of genes. Some plants are polyploid. |
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Term
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Definition
Proteins associated with DNA. A component of chromatin. The 5 major types are H1, H2a, H2b, H3, and H4. Present in almost all cells. |
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Term
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Definition
The protein found in the place of histones in sperm cells. |
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Term
Nonhistone chromosomal proteins |
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Definition
Proteins associated with DNA. A component of chromatin. Play a role in gene expression. Scaffold proteins. |
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Term
Multineme/Multistrand model |
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Definition
A model of how DNA forms chromosomes that says it runs back and forth parallel over the length of the chromosome. |
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Term
Unineme/Single-strand model |
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Definition
A model of how DNA folds into chromosome that says it curls up tightly and runs the chromosome length one time. |
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Term
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Definition
Fibres 30 nm in diameter resulting from nucleosome fibres folding up. There are two models of how they fold: solenoid and zig-zag. |
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Term
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Definition
A structure of nonhistone chromosomal proteins that is revealed in a mitotic chromosome if you remove the histones. It is a skeleton roughly in the shape of the chromosome, with the DNA in a puddle all around it. |
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Term
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Definition
The segment of the mitotic chromosome where the mitotic spindle attaches to it. Structure varies from species to species. In humans it is a sequence of 5000 to 15000 copies of the 171 nucleotide alpha satellite sequence. In yeasts, it is only 110 base pairs long. During prometaphase kinetochores attach to its outer surface, and then attach to microtubules. |
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Term
Alpha/Alphoid satellite sequence |
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Definition
A DNA sequence where the centromere is on a mitotic chromosome. |
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Term
Huntington Willard and colleagues |
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Definition
Showed that the minimum number of nucleotides needed for a the alpha satellite sequence to make a centromere is 450000. |
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Term
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Definition
Telo = end, meros = part. The end of a eukaryotic DNA strand. They prevent the DNA from degrading, fusing with other DNA, and facilitate replication without loss of materials. The sequence that repeats before a telomere in vertebrates is TTAGGG. The number of repetitions varies greatly between species. As an individual ages, the number goes down. Between 500 and 3000. They end with a G rich single strand on the 3' end that loops over into a T-loop, aided by shelterin. |
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Term
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Definition
Coined the term "telomere" in 1938. Showed that without natural ends, the chromosome cannot produce progeny. |
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Term
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Definition
Demonstrated tht the new ends of broken chromosomes are sticky an tend to fuse to each other, but natural ends are stable and non-sticky. |
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Term
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Definition
The structure formed in a telomere by the single 3' end, aided by shelterin. |
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Term
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Definition
A 6 protein complex that aids in the formation of T-loops in telomeres. |
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Term
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Definition
Keeps telomere sequences from getting shorter. Cancer cells and embryos have this. |
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Term
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Definition
Conducted an experiment with mice where they are introduced to smooth and rough bacteria. Only the smooth type is lethal, but rough type can kill a mouse if smooth DNA (dead organisms, or purified DNA), is present along with living rough cells. |
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Term
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Definition
(1822-1884) The scientist and monk who in 1865 showed that genes (he called them "Merkmlen") transmit genetic information. Used garden peas for his studies. |
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Term
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Definition
The material that is passed from parent to offspirng, carrying information. It was long thought to maybe be proteins, but turned out to actually be nucleic acids. It has 3 functions:
1. Genotypic function (replicte, accurately pass on information)
2. Phenotypic function (gene expression, control development of organism)
3. Evolutionary function (mutations, produce variation so that evolution can continue) |
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Term
Richard Sia and Martin Dawson |
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Definition
In 1931 they did Frederick Griffith's experiment in vitro and found that mice play no role in the transformation process of rough bacteria into smooth bacteria. |
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Term
Oswald Avery, Colin MacLeod, and Maclyn McCarty |
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Definition
The group of scientists who demonstrated that the transforming principle in Frederick Griffith's experiment was DNA. They did this by using protease, RNase, and DNase on different groups. Only the group treated with DNA failed to transform into smooth bacteria. However, it is difficult to prove the purity of DNA, so DNA was not quite proven to be the genetic material. |
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Term
Alfred Hershey and Martha Chase |
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Definition
Won the Nobel Prize in 1969. Did an experiment that showed that genetic material in bacteriophage T2 is DNA. Used isotopes and a blender to show that it is DNA that is injected into the host, and protein remains outside. |
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Term
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Definition
Where pure virus DNA was added to E. coli, and normal bacteriophages were produced. Proves that DNA is the genetic material. |
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Term
Heinz Fraenkel-Conrat and colleagues |
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Definition
In 1957 they did an experiment on tobacco mosaic virus. They swapped the protein and DNA of two strains, and found that it is the DNA that affects the type of bacteriophage produced. |
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Term
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Definition
When a cell divides into two cells, eventually creating a clone. A mother cell becomes two daughter cells. |
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Term
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Definition
A cluster of cells that are genetically identical to each other. |
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Term
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Definition
The relatively large cell that splits into two, becoming two daughter cells. |
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Term
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Definition
The two cells that form from the mother cell in cell division. |
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Term
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Definition
A clone of cells large enough to be seen by the naked eye. |
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Term
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Definition
The lifecycle of cells. It goes G1, S, G2, M, then it repeats. May be as short as half an hour to as long as many months. If proteins that control this process are disrupted, cell division can become uncontrolled, could lead to cancer. |
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Term
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Definition
Synthesis phase. DNA synthesis occurs, replicating all the DNA. Takes about 9 hours, depending on the cell. At the end of this phase there is a check-point to make sure all the DNA has been replicated correctly. |
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Term
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Definition
M phase. Greek for "thread". The cell contents are distributed equally between two daughter cells. During this phase chromosomes resemble tiny threads. |
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Term
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Definition
The final phase of mitosis. The physical splitting process in mitosis. In plants a cell wall is formed between the two cells. In animal cells, the plasma membrane is pulled inwards until fission occurs. |
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Term
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Definition
Gap phase 1. The cell grows in size. Cellular metabolism. At the end there is a check point where the cell "decides" whether or not to divide based on its surroundings, physical condition, and cell type. If yes, it enters S phase. If no, it becomes quiescent and enters G0 phase. |
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Term
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Definition
The period between mitotic events. G1, S, and G2. During this phase the chromosomes are mixed up with each other and are indistinguishable. The centrosome is duplicated. |
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Term
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Definition
Duplicated chromosomes carrying identical genes. Formed during S phase. |
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Term
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Definition
Microtubules formed from the MTOC. They split up and correctly distribute daughter cells. |
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Term
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Definition
The first phase in mitosis. The spindle formation starts and the chromosomes are condensed. Endomembrane organelles and the nuclear envelope are fragmented into vesicles which attach to kinetochores. The nucleoli disappear. |
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Term
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Definition
Two components of the centrosome algined at right angles to each other. Surrounded by a matrix that initiates the formation of the mitotic spindle during prophase. |
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Term
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Definition
Proteins associated with the centrosomes. Its outer region binds to the microtubule with corona fibres and its inner region binds to the centromere during prometaphase. |
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Term
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Definition
The second phase in mitosis. Kinetochores attach to microtubules. The chromosomes are aligned into the metaphase plate position. |
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Term
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Definition
The plane along which chromosomes are lined up during metaphase. It is halfway between the two spindle poles. |
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Term
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Definition
The third phase in mitosis. The sister chromatids detach from each other and are pulled to separate poles. Microtubules shorten, pulling the chromatids (now called chromosomes). |
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Term
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Definition
The fourth phase in mitosis. The chromosomes decondense. The fractured organelles begin to re-establish themselves. The nuclear envelope reforms from the vesicles. |
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Term
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Definition
Gap phase 2. The cell prepares for mitosis. |
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Term
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Definition
A phase after G1 that occurs in cells that decided not to reproduce at the checkpoint after G1. They may later on enter G1. |
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Term
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Definition
A word describing cells that are in an extended G0 period. They will virtually never enter G1 phase. |
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Term
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Definition
Protein involved in the condensing of chromosomes during mitosis. Creates small loops of cromatin fibre. |
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Term
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Definition
A protein involved in the condensation of chromosomes in mitosis. Attaches two parallel chromatin fibres. |
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Term
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Definition
A phase of mitosis between prophase and metaphase. Chromosomal microtubules attach to kinetochores, which are on the outer surface of the centromeres. |
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Term
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Definition
When bacteria take up DNA from their neighbors or surroundings through a plasmid. Only prokaryotes can do it. This was observed in Frederick Griffith's experiments. |
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Term
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Definition
Homo sapiens. Have 23 chromosomes. Cannot be used as model organisms since that would be unethical. However human cells can be cultured and studied.
It is hard to study human genetics because humans make few progeny, and you cannot test-cross them. Instead you must analyse family histories. |
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Term
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Definition
Fibres that attach a kinetochore to the microtubule. |
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Term
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Definition
Greek for "diminuition". Diploid cells duplicate chromosomes then split twice, becoming haploid. There is meiosis I and II. Produces gametes or cells that then divide to become gametes. Crucial in sexual reproduction.
It is similar to mitosis, but twice. Prophase I is split into 5 stages. The chromatids are spliced randomly. There are countless different possible combinations of genes that can be produced. |
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Term
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Definition
Chromosomes that carry the same genes in diploid cells. The two may have different alleles. One is inherited from the mother and one from the father. They associate with each other during meiosis. |
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Term
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Definition
Chromosomes that carry different genes. |
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Term
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Definition
The first prophase in meiosis. It is split into 5 parts: leptonema, zygonema, pachynema, diplonema, and diakenesis. |
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Term
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Definition
The first stage in prophase I. "Thin threads". Duplicated chromosomes condesnse. |
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Term
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Definition
The second stage in prophase I. "Paired threads". Homologous chromosomes come together in synapsis. |
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Term
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Definition
The joining together of two homologous chromosomes during zygonema. The synaptonemal complex is involved. |
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Term
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Definition
A protein complex involved in the synapsis of homologous chromosomes during zygonema. It is 3 parallel rods, two lateral elements and one central element. Lateral elements are connected to the central element by rungs.
Sometimes this structure is absent in meiosis. |
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Term
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Definition
The two rods in the synaptonemal complex that associate with each chromosome. They are attached to the central element by rung-like structures. |
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Term
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Definition
The rod structure in synaptonemal complex that is in between the two lateral elements. It is connected to them by rung-like structures. |
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Term
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Definition
The third stage of prophase I. "Thick threads". Paired chromosomes can now be seen by a light microscope. Crossing-over occurs. |
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Term
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Definition
A pair of chromatids. 2 chromatids total. |
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Term
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Definition
A pair of chromosomes. 4 chromatids each. |
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Term
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Definition
The process of breaking tetrad of chromosomes at the chiasmata, then fixing it, swapping random pieces between the two. It involves only two of the four chromatids. |
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Term
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Definition
The fourth stage of prophase I. "Two threads". The paired chromosomes separate, but remain attached at their chiasmata. This stage can last a very long time. In human females, up to 40 years. |
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Term
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Definition
"Cross". The points on a tetrad of chromosomes where it is broken during crossing-over. During diplonema the chromosomes are attached at these points. |
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Term
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Definition
The fifth stage of prophase I. "Movement through". The chromosomes condense further, then the nuclear membrane fragments and the spindle apparatus attaches to kinetochores on chromosomes. |
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Term
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Definition
Metaphase in the first division of meiosis. The paired chromosomes orientate along the metaphase plate. At the end of the phase, the chiasmata undergo terminalization. |
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Term
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Definition
The chiasmata of chromosomes slip away during metaphase I. |
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Term
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Definition
The anaphase of the first division in meiosis. The paired chromosomes separate in chromosome disjunction.
In heterozygotes are two equall likely options for this:
1. AA and BB on one side, aa and bb on the other. Produces 2 AB and 2 ab gametes.
2. AA and bb on one side, aa and BB on the other. Produces 2 Ab and 2 aB gametes. |
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Term
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Definition
The separation of chromosomes mediated by spindle apparatus in anaphase I and II. |
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Term
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Definition
The telphase of the first division in meiosis. The spindle apparatus disassesmbles, the daughter cells are separated by a membrane, the chromosomes decondense, and a nucleus forms around each daughter cell.
Sometimes this stage is skipped. |
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Term
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Definition
The prophase of the second division in meiosis. Chromosomes attach to a new spindle apparatus. |
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Term
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Definition
The metaphase of the second division in meiosis. Chromosomes arrange along the metaphase plate. |
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Term
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Definition
The anaphase of the second division in meiosis. Chromosome disjunction. Sister chromatids move to opposite poles. |
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Term
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Definition
The telphase of the second division in meiosis. The separated chromatids (now called chromosomes) gather at te poles. Nuclei form around them. |
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Term
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Definition
The haploid spore produced by Baker's yeast in its ascus. |
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Term
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Definition
A sac on Baker's yeast where the ascospores are made. |
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Term
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Definition
The diploid stage in the lifecycle. This is usually the dominant stage. The mature plant. It produces haploid gametophyte spores. |
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Term
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Definition
A plant organ atop of the stamen where microspore mother cells undergo meiosis to form microspores. |
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Term
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Definition
The male organs of a plant. The anther is found at the top of it. Microspores are made. |
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Term
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Definition
The cells found in plant anthers that undergo meiosis to form microspores. |
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Term
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Definition
The male gametes in plants. Formed from microspore mother cells in the anther. They undergo mitosis to form pollen grains. |
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Term
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Definition
The male gametophyte of plants. Two sperm cells inside a vegetative cell. |
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Term
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Definition
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Term
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Definition
The plant organ at the bottom of the pistil where the megaspore mother cells undergo meiosis to form four megaspores.
OR
The female gonad in animals. Oogenesis occurs here. |
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Term
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Definition
The visible female plant organ. Pollen lands on it for feritlization. |
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Term
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Definition
Cells found in the plant ovary that undergo meiosis to form four megaspores. |
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Term
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Definition
The female gametes of plants. Formed from the megaspore mother cells. Four are formed, but only one survives. It undergoes mitosis to form the eight haploid cells of the embryo sac. |
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Term
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Definition
The female gametophyte in plants. Eight cells formed from the surviving megaspore. There is one egg, two synergids, two polar nuclei, and three antipodal cells. |
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Term
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Definition
In plants, one of the haploid cells formed by the surviving megaspore. It resides near the bottom of the embryo sac. It is fertilized by one of the sperm to form the diploid zygote in fertilization.
OR
In animals, the female gamete formed by oogenesis from the oogonia in the ovaries. Four cells are formed by the oogonia, but only one becomes the egg. |
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Term
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Definition
Two of the eight cells formed by the surviving megaspore. They reside near the bottom of the embryo sac. |
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Term
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Definition
Three of the eight cells formed by the surviving megaspore. They reside near the top of the embryo sac and degrade away. |
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Term
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Definition
Two of the cells formed by the surviving megaspore. Actually they don't separate from each other by cytokinesis, so they are more like one cell with two nuclei. Together they are diploid. It is fertilized by a sperm, forming a triploid endosperm. |
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Term
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Definition
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Term
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Definition
In plants, there are two in one pollen grain. One fertilizes the egg, forming a diploid zygote. The other fertilizes the polar nuclei, forming a triploid endosperm.
OR
In animals, they are the male gametes. Formed by spermatogenesis from spermatogonia in the testes. They have flagella and swim. |
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Term
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Definition
The diploid cell formed by the egg when it is fertilized by a sperm. It will grow into the sporophyte in plants.
In mammals all of the cytoplasmic contents, including mitochondria, are inherited from the mother (the egg). |
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Term
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Definition
The triploid structure formed by the polar nuclei when they are fertilized by a sperm. It helps the plant during early development. |
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Term
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Definition
The formation of gametes. Occurs in the gonads. Oogenesis for females, spermatogenesis for males. |
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Term
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Definition
The organs where gametogenesis occurs. Ovaries for females, testes for males. |
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Term
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Definition
The formation of eggs occuring in the animal ovaries. Oogonia undergo meiosis, forming four cells. Only one cell becomes the egg. |
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Term
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Definition
The cells found in the ovaries that undergo meiosis to form four cells, one of which becomes the egg. |
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Term
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Definition
The production of sperm that occurs in the male gonads, the testes. Spermatogonia undergo meiosis, producing sperm. The four cells produced don't fully detach. They form a spermatid. |
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Term
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Definition
The male gonads. Spermatogenesis occurs here. |
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Term
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Definition
The cells in the testes that undergo meiosis to form sperm. |
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Term
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Definition
The chromosomes that determine the sex of the organisms. In humans it is the 23 pair. XX is female. XY is male. One X is inherited from the mother, and either an X or a Y is inherited from the father.
There are only 2 genes needed on the Y chromosome to work properly. They made a perfectly viable male mouse with only 2 Y chromosome genes. |
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Term
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Definition
Also called reduction division. The first division in meiosis. Prophase is split into 5 stages. Produces two diploid daughter cells tht are genetically different. |
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Term
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Definition
The second division in meiosis. The two genetically different diploid cells produced in meiosis I both divide, creating genetically different haploid cells.
In mammal oogenesis, this stage is triggered by ovulation, and the process doesn't fully finish until fertilization occurs. |
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Term
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Definition
A spermatogonia that has fully duplicated its DNA and is ready to undergo meiosis. |
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Term
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Definition
The two cells produced by meiosis I in spermatogenesis. They don't fully separate and are connected by a cytoplasmic bridge. It undergoes meiosis II to form a spermatid. |
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Term
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Definition
The four haploid cells produced by spermatogenesis. They never fully separate, and are connected by ctoplasmic bridges while the sperm cells develop. |
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Term
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Definition
An oogonium that has fully replicated all of its DNA and is ready to undergo meiosis. |
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Term
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Definition
A diploid oogonium that has undergone meiosis I. |
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Term
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Definition
Cells produced by oogensis. They are the 3 cells that don't make it and don't become an egg in oogenesis. |
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Term
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Definition
The haploid life stage. With a few exceptions (like moss), this stage is the non-dominant stage. There are male gametophytes (pollen) and female gametophytes (embryo sac). When opposite gametophytes meet they create a genetically unique, new sporophyte.
In moss the gametophyte stage is the furry moss. |
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Term
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Definition
Non-sex chromosomes. In humans pairs 1 through to 22. |
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Term
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Definition
Pisum sativum. A model organism that Mendel used in his studies. They have both male and female organs on their flowers. The petals close tightly, preventing pollen from entering or leaving, supporting self-fertilization. They are highly inbred for this reason. |
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Term
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Definition
When a plant self-fertilizes for many generations, causing its genotype to be homozygous. Garden peas show this. |
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Term
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Definition
Mendel did this with peas by removing the anthers of the "mother" and applying pollen from the "father" onto the pistil. It doesn't matter which is the father or mother (by genotype), the progeny will have the same ratios of genotypes. |
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Term
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Definition
The allele that is not expressed in a heterozygous individual. It is only expressed if homozygous. Symbolized by the lower case letter of that gene. In a pedigree, each colour individual does not have colour parents. More likely to show up when there is inbreeding. |
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Term
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Definition
The allele that is expressed in a heterozygous individual. Symbolized by the upper case letter of the gene. In a pedigree each colour individual has at least one colour parent. |
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Term
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Definition
A cross looking at only one trait. |
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Term
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Definition
Word was coined by Wilhelm Johannsen. The inherited fators in reproduction. Have dominant or recessive alleles. Symbolized by two letters; upper case if dominant, lower case if recessive. The allele inherited from the mother is written first.
Defined as a transcribed region of DNA. |
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Term
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Definition
In 1909 coined the term "gene". |
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Term
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Definition
Forms of a gene. Can be dominant or recesive. |
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Term
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Definition
Having two of the same allele for a gene. Produces one kind of gamete. |
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Term
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Definition
Having two different alleles for a gene. Only the dominant allele is expressed. The recessive allele is "hidden". Produces equal amounts of the two gametes. |
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Term
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Definition
The genes of an individual, regardless of what alleles are expressed. Examples: AA, Aa, aA, aa. |
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Term
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Definition
The physical appearance of an individual regardless of genes. The dominant allele is expressed. |
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Term
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Definition
The parental strain. In Mendel's experiments these were highly inbred, homozygous peas. |
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Term
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Definition
The progeny of the parental generation. F1 is heterozygous, and F2 (the self-fertilizing progeny of F1), contain a wide variety of genotypes. |
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Term
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Definition
Do not mix. Mendel found that alleles are segregate. They do not mix with each other during the reproduction process, as previously thought. |
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Term
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Definition
In a heterozygote, the dominant allele is expressed, concealing the presence of the recessive allele. |
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Term
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Definition
In a heterozygote, the two alleles are segregate from one another and do not mix or combine at any point. |
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Term
Principle of Independent Assortment |
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Definition
The alleles of different genes assort indepentently of each other during reproduction. Only applies if the genes are on separate chromosomes. If on the same chromosome, the further apart the two genes are, the more likely they will assort independently. |
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Term
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Definition
A cross looking at two genes. Mendel used this experiment to base the Principle of Independent Assortment. The two genes assort independently of each other, forming a larger variety of different possible genotypes than in a monohybrid cross. |
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Term
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Definition
A method of calculating genotype/phenotype frequencies from a cross. Used when there are one or two genes. Invented by R. C. Punnett.
A table is made showing the possible combinations of gametes. |
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Term
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Definition
A method for calculating the frequencies of genotypes/phenotypes of a cross. Used when there are two or more genes being looked at. The possible combinations of each gene are run through in a forked line. The frequencies of each phenotype are then multiplied together for each path to find the frequency of phenotype combinations. |
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Term
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Definition
A method used to calculate the frequencies of genotypes. Uses logic and math. Use probability rules. Used when there are many genes being taken into account. |
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Term
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Definition
A fixed position on a chromosome. Plural = loci. |
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Term
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Definition
The shorter arm on a chromosome. |
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Term
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Definition
The longer arm on a chromosome. |
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Term
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Definition
A rule of probability.
The probability that two or more events will occur together is equal to the product of the probabilites of the events. |
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Term
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Definition
A rule of probability. If two events are independent, the probbaility that at least one of them will occur is the sum of their individual probabilities. To get the probability of only one occuring, subtract from this the product of the probabilities. |
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Term
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Definition
A cross with a homozygous recessive individual. Used to determine if the individual is homozygous or heterozygous. |
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Term
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Definition
A diagram showing the relationships among family members with phenotypes.
Diamond = sex unspecified
Circle = female
Square = male
Colour = has trait
Blank = does not have trait
Crossed out = deceased
Number = number of children of the sex.
Roman numerals = generation number
Arabic numerals = individual within a generation |
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Term
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Definition
When there are only two possible phenotypic possibilities. |
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Term
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Definition
A person who interviews parents, relatives, and researches family history. Uses genetic observations to predict outcomes of children for family planning purposes. Often use by people who have heritable diseases in their families. |
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Term
Nonpolypod colorectal cancer |
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Definition
A hereditary diseaes. A dominant trait. Appears around age 40, so it is hard to tell if an individual carries it, especially at an age when they are planning a family. |
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Term
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Definition
A recessive trait where there is no melanin in the skin, eyes, or hair. |
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Term
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Definition
The code used by computers. It uses only 1s and 0s. |
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Term
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Definition
The process of transfering the informaion from DNA to RNA. This can sometimes go backwards (RNA to DNA) in virus tumor cells.
RNA is synthesized 5' first. Ribonucleotides are added to the 3' end. The reaction is catalyzed by RNA polymerase. Has 3 steps: Initiation, Elongation, and Termination. |
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Term
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Definition
The process of transfering information in RNA into protein. Protein can never turn back into RNA. It has 3 stages: Initiation, Elongation, and Termination. |
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Term
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Definition
The code by which RNA is converted to protein during translation. Properties:
1. Codons are 3 nucleotides. Each codon specifies one amino acid.
2. Each nucleotide belongs to one codon.
3. There is no punctuaton in coding regions.
4. Except for methionine and tryptophan, all amino acids have degeneracy.
5. Codon sequence for same or similar (by properties) amino acids are similar.
6. There are start and stop codons.
7. Genetic code is universal. There are only minor exceptions (mitochondria, protozoa). |
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Term
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Definition
The primary RNA product of DNA transcription. In prokaryotes this is used as mRNA. In eukaryotes the primary transcription is pre-mRNA. |
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Term
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Definition
The primary transcription in eukaryotes. It has its introns removed before being used as mRNA. |
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Term
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Definition
Sequences in mRNA that are expressed turing translation. They are not removed during pre-mRNA modification. |
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Term
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Definition
A pre-mRNA sequence that is not expressed during translation. It is removed beforehand by slicing reactions on spliceosomes. |
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Term
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Definition
Reactions that remove the introns from pre-mRNA. Occurs on a spliceosome. |
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Term
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Definition
Where splicing reactions occur. It is made from snRNA. |
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Term
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Definition
RNA found in ribosomes. It has structural and catalytic functions. I eukaryotes it is transcribed by RNA polymerase I, except for 5S rRNA, which is transcribed by RNA polymerase III. |
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Term
Small Nuclear RNA (snRNA) |
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Definition
The structural component of spliceosomes. In eukaryotes it is transcribed by RNA polymerase III. |
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Term
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Definition
Short nucleotides that block the expression of complementary mRNA by causing degradation or by repressing translation. |
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Term
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Definition
The strand of DNA that is complementary to the RNA being synthesized during transcription. |
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Term
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Definition
The strand of DNA which is identical to the RNA strand being synthesized during transcription. |
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Term
|
Definition
A strand of RNA that makes "sense" when translated into proteins. These are the sequences used as mRNA. |
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Term
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Definition
A strand of RNA complementary to a sense strand. They are transcribed by RNA polymerase V. |
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Term
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Definition
The machinery in prokaryotes that catalyzes RNA synthesis during transcription. It binds to DNA sequences called promoters. It creates the transcription bubble. In prokaryotes the complete RNA polymerase is called a holoenzyme.
Eukaryotes have 5 different RNA polymerases. Eukaryotic RNA polymerase are much larger and require transcription factors. |
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Term
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Definition
A DNA sequence to which RNA polymerase binds to. It is nearby to the transcription site, usually upstream. They only work in one DNA orientation. They are more complex in eukaryotes than in prokaryotes. |
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Term
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Definition
The locally unwound segment of DNA during transcription. It is unwound and then rewound by RNA polymerase. In E. coli it is 18 nucleotides is size. |
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Term
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Definition
A segment of DNA that is transcribed into RNA. Can be one or more genes. |
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Term
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Definition
Regions near to the 5' on RNA. |
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Term
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Definition
Regions near the 3' end on RNA. |
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Term
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Definition
The complete RNA polymerase in prokaryotes. It has one alpha (α) subunit, one sigma (σ) subunit, and two beta (β) subunits, β and β'. |
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Term
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Definition
A component of a holoenzyme that is used to make the tetrameric core. |
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Term
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Definition
The segment of the holoenzyme that includes the alpha subunit and both beta subunits. Lacks the sigma factor. It completes the entire transcription elongation step without the sigma factor. |
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Term
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Definition
A component of the tetrameric core in a holoenzyme that contains the ribonucleoside triphosphate binding site. |
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Term
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Definition
A component of the tetramric core in a holoenzyme that contains the template DNA binding site. |
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Term
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Definition
The subunit in a holoenzyme that binds to promoters or transcription initiation sites on the DNA. After about 8 to 9 nucleotides are bound together, it falls off. A few short nucleotide segments may be released prior to this. |
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Term
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Definition
Sequences upstream from the transcript initation site. Have negative prefixes. |
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Term
|
Definition
DNA sequences downstream from the transcription initiation site. Have positive prefixes. |
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Term
|
Definition
A sequence that is conserved from species to species, such as -35 or -10 sequences. |
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Term
-35 sequence/Recognition sequence. |
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Definition
A consensus sequence located at -35. It's nontemplate sequence is TTGACA. It is recognized by the sigma factor and binds to it. |
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Term
|
Definition
A consensus sequence located at -10. Its nontemplate sequence is TATAAT. It facilitates the localized unwinding of DNA, since it is rich in wekaer A-T bonds, it is easier to unwind. |
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Term
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Definition
Begins when the sigma factor is released. RNA elongation occurs inside the transcription bubble. |
|
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Term
Transcription termination |
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Definition
Occurs when RNA polymerase encounters a termination signal. |
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Term
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Definition
A DNA sequence that terminates transcription. It can be rho-dependent or rho-idependent. |
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Term
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Definition
A termination signal that only works if rho protein is present. There is a rut upstream from it where rho attaches to the RNA. A hairpin forms in the RNA. When rho reaches the hairpin, rho detaches the RNA from the DNA. |
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Term
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Definition
A 50 to 90 nucleotide long sequence that binds to rho protein during rho-dependent termination. |
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Term
Rho-independent terminator |
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Definition
A terimation signal that works with or without rho. It is a sequence high in A-T downstream from the hairpin. RNA polymerase slows down due to the hairpin, then it falls off due to A-T's weak bonds. |
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Term
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Definition
When a single mRNA contains multiple genes. Prokaryotes often have mutligenic mRNA. |
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Term
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Definition
When a single mRNA has only one gene. Eukaryotes often have monogenic mRNA. |
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Term
7-methyl guanosine (7-MG) caps |
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Definition
Caps added to the 5' end of pre-mRNAs. They are added during transcription when the nascent RNA is around 30 nucleotides long. CBPs attach to the cap. The cap protects the RNA from degradation by nucleases. |
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Term
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Definition
Tails added to the 3' end of pre-mRNA as soon as it emerges. It is a tract of As 20 to 200 nucleotides long. It is added by Poly (A) polymerase in polyadenlyation. |
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Term
Heterogeneous nuclear RNA (hnRNA) |
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Definition
mRNA in eukaryotes that has yet to be modified (7-MG caps, Poly (A) tails, introns spliced out). It is transcribed by RNA polymerase II. |
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Term
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Definition
Present in most eukaryotes. Found in the nucleolus. Produces rRNA except for 5S rRNA. |
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Term
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Definition
Found in most prokaryotes. It transcribes hnRNA (which then becomes mRNA). It recognizes TATA boxes. |
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Term
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Definition
Found in most eukaryotes. It transcribes 5S rRNA, tRNA, and snRNA. |
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Term
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Definition
The chemical modification of histone tail proteins. Turns off transcription genes. RNA polymerases IV and V are involved in it. Nucleosomes are unwound. ATP is consumed. Nucleosomes can slide along DNA, change spacing, or become temporarily displaced. |
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Term
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Definition
Found in plants and some fungi. Involved in chromatin remodeling. It synthesizes siRNA. |
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Term
Small Interfering RNA (siRNA) |
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Definition
RNA that regulates gene expression. Interacts with proteins during chromatin remodeling. It is transcribed by RNA polymerase IV. |
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Term
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Definition
Found in plants and some fungi. It is involved in chromatin remodeling. It synthesizes antisense strands of genes that are regulated by siRNAs. |
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Term
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Definition
Necessary for transcription intitiation in eukaryotes. They bind to the promoters and form initiation complexes that the correct RNA polymerase can bind to. There are basal transcription factors, enhancers, and silencers. |
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Term
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Definition
A conserved promoter RNA sequence near the transcription site that is recognized by RNA polymerase II. The sequence is 5'-TATAAAA-3'. |
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Term
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Definition
A conserved promoter RNA sequence at -80 that is recognized by RNA polymerase II. The sequence is 5'-GGCAATCT-3'. |
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Term
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Definition
A conserved promoter RNA sequence that influences the efficiency of promotors. The sequence is 5'-GGGCGG-3'. |
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Term
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Definition
A conserved promoter RNA sequence that influences the efficiency of promotors. The sequence is 5'-ATTTGCAT-3'. |
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Term
Basal transcription factor |
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Definition
A transcription factor that interacts with promotors, causing initiation. Influenced by special transcription factors. |
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Term
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Definition
Transcription Factor for RNA polymerase II D. The first basal transcription factor. It has a TBP and TBP associated proteins. |
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Term
TATA-binding protein (TBP) |
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Definition
Protein that binds to the TATA box. It is found in TFIID. |
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Term
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Definition
Transcrition Factor for RNA polymerase II A. The second basal transcription factor. |
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Term
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Definition
Transcrition Factor for RNA polymerase II B. The third basal transcription factor. |
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Term
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Definition
Transcrition Factor for RNA polymerase II F. It binds to RNA polymerase II, then it becomes the fourth basal transcription factor. It has two subunits, one of which is DNA unwinding. |
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Term
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Definition
Transcrition Factor for RNA polymerase II E. The fifth basal transcription factor. It binds to downstream DNA. |
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Term
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Definition
Transcrition Factor for RNA polymerase II H. The sixth basal transcription factor. It travels wiht the RNA polymerase II during transcription, unwinding the transcription bubble. |
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Term
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Definition
Transcrition Factor for RNA polymerase II J. The seventh basal transcription factor. |
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Term
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Definition
FAcilitates Chromatin Transcription
A protein complex that allows RNA polymerase to pass over nucleosomes. It removes the H2A/H2B histones, leaving hexasomes. After RNA polymerase is done, it restores them. |
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Term
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Definition
Adds Poly(A) tails to RNA in polyadenlyation. |
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Term
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Definition
The process of adding Poly(A) tails to RNA. Done by Poly (A) polymerase. |
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Term
aminoacyl-tRNA synthetase |
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Definition
An enzyme that attaches amino acids to their correct tRNAs, making aminoacyl-tRNA. |
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Term
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Definition
Initiation Factor 1. It attaches the IF-2/methionyl-trNAfMet and mRNA/30S/IF-3 complexes together with GTP in prokaryote translation intitiation. It falls off when the 50S attaches. |
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Term
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Definition
Inititaion Factor 2. It attaches to methionyl-tRNAfMet in prokaryote translation initiation. |
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Term
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Definition
Initiation Factor 3. It attaches to mRNA and 30S in prokaryote translation initiation. It controls 30S's ability to start the initiation process. |
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Term
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Definition
The aminoacyl-tRNA that recognizes the initiation codon in prokaryotes. The f stands for its formyl group. It interacts with IF-2. It recognizes the AUG initiation codon. |
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Term
Translation Initiation (prokaryote) |
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Definition
1. IF-2 and methionyl-tRNAfMet join together.
2. mRNA, 30S, and IF-3 join together. mRNA and 30S are joined by the Shine-Dalgarno sequence.
3. The two components come together with IF-1 and GTP.
4. 50S is added, forming a complete 70S. The GTP is hydrolysized and IF-1 and IF-3 fall off. |
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Term
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Definition
AGGAGG. 30S and the mRNA are base-paired with this sequence on the mRNA during prokaryote translation initiation. |
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Term
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Definition
The aminoacyl-tRNA that recognizes the intitiation codon in eukaryotes. It is not formylated. |
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Term
Translation Initiation (eukaryote) |
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Definition
Initiation complex scans the mRNA starting at the 5' end for the initiation sequence, rather than attaching at the Shine-Dalgarno sequence. For optimal translation, there is the Kozak's rules.
When the initiation sequence is found, initiation factors detach and the 60S unit attaches, forming the 80S ribosome. |
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Term
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Definition
The RNA sequence most optimal for translation initiation in eukaryotes. 5'-GCC(A/G)CCAUGG-3'. Named after Marilyn Kozak. |
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Term
Cap-binding protein (CBP) |
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Definition
A protein that binds to the 7-MG cap on mRNAs in eukaryotes. |
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Term
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Definition
1. Aminoacyl-tRNA binds to the A site. Turns EF-Tu-GTP into EF-Tu-GDP.
2. The polypeptide chain is transfered from P site to A site by forming a polypeptide bon. Causes the P site amino acid to detach from its tRNA. Catalysed by peptidyl transferase.
3. Ribosome moves 3 nucleotides down the mRNA. tRNA in the A site moves to P site, et cetera. Uncharged tRNA in the E site falls off. Requires EF-G and the hydrolysis of GTP.
4. Repeat! |
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Term
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Definition
The "downstream" of the thre sites on a ribosome. |
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Term
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Definition
The middle of the three sites on a ribosome. |
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Term
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Definition
The "upstream" of the three sites on a ribosome. |
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Term
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Definition
Elongation Factor Tu with GTP. It is used to attach an aminoacyl-tRNA (all excet methionyl-tRNA) to the A site of a ribosome. GTP is hydrolyzed, making it EF-Tu-GDP. It converts back to EF-Tu-GTp using EF-Ts. |
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Term
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Definition
Elongation Factor Ts.
It turns EF-Tu-GDP into EF-Tu-GTP. |
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Term
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Definition
An enzyme built into the 50S of a ribosome. It catalyzes the formation of a peptide bond between the amino acids in sites P and A. |
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Term
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Definition
Elongation Factor G. Necessary for the 3rd step of elongation when the ribosome moves 3 nucleotides down the mRNA. |
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Term
Oscar Miller, Barbara Hamkalo, and colleagues. |
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Definition
Visualized the elongation of fibrion silk fibre using electron microscopy. This protein doesn't fold as it is translated. |
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Term
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Definition
AUG or GUG. It is recognized by methionyl-tRNAfMet in prokaryotes and methionyl-tRNAiMet in eukaryotes. GUG is recognized by a valine tRNA. In prokaryotes it must be followed by the Shine-Delgarno sequence in order to initiate. |
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Term
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Definition
UAA, UAG, or UGA. Recognized by an RF. |
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Term
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Definition
It recognizes a termination codon. It attaches a water molecule to the polypeptide rather than an amino acid, causing it to fall off and the ribosome to break up. |
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Term
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Definition
Release Factor 1. Found in prokaryotes. It recognizes UAA and UAG termination codons. |
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Term
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Definition
Release Factor 2. A release factor in prokaryotes. It recognizes UAA and UGA termination codons. |
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Term
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Definition
The release factor in eukaryotes. It recognizes all three termination codons. |
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Term
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Definition
When one amino acid has more than one codon that can code for it. Evolved so that even if there is a mutation, it will probably not be lethal, and in most cases will have no effect at all. Even if the wrong amino acid is translated, the wrong amino acid is likely to have similar properties, and not have any great effect on protein function. |
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Term
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Definition
When the third base in a codon may be either two of the pyrimidines or either two of the purines, and it wouldn't effect the amino acid that is translated. |
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Term
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Definition
When the third base of a codon may be any base without changin the amino acid that is translated. |
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Term
Friancis Crick and colleagues |
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Definition
In 1961 they came up with solid evidence for there being 3 nucleotides to a codon. They used proflavin, a mutagenic agent that caused additions or deletions in DNA. The mutations could be reversed by suppressor mutations. If there are three of the same type of mutation, there is no change to phenotype. |
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Term
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Definition
Mutations that are able to restore addition/deletion mutations that alter the reading frame of translation. It is the opposite of the first mutation. |
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Term
Marshall Nirenberg, Severo Ochoa, H. Ghobind Khorana, Philip Leder, and colleagues. |
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Definition
Deciphered the genetic code. In 1968 Nirenberg and Khorana won the Nobel Prize. |
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Term
Central dogma of molecular biology |
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Definition
DNA is transcribed into RNA and RNA is translated into protein. |
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Term
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Definition
Severs RNA at its 3' end. |
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Term
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Definition
A spontaneous mistake in DNA that is heritable. Can refer to the change in genetic material or the process by which the change occurs. It is the source of all genetic variability. It drives evolution. Too much muation can disrupt transfer of genes. Mechanisms have evolved to regulate mutation levels.
Not to be confused with the recomibination of existing genes. |
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Term
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Definition
An organism with a mutation. Shows a phenotype that is less than 1% of the population. |
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Term
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Definition
A mutation at a specific site in a gene: substitution, inertion, or deletion. |
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Term
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Definition
The common forms of thymine and guanine. |
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Term
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Definition
The rare forms of thymine and guanine. |
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Term
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Definition
The common forms of cytosine and adenine. |
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Term
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Definition
The rare forms of cytosine and adenine. |
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Term
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Definition
The replacement of a purine with a purine or the replacement of a pyrimidine with a pyrimidine. There are 4 possible transitions. |
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Term
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Definition
The replacement of a purine with a pyrimidine or the replacement of a pyrimidine with a purine. There are 8 possible transversions. |
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Term
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Definition
A mutation that alters the reaing frame of the gene. Almost always result in synthesis of non-functional proteins. Occurs due to inaccuracy of DNA replication, or exposure to mutagenic agents. |
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Term
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Definition
In 1927 proved that X rays induce mutations in fruit flies. Won the Nobel Prize in 1946. Looked at the ClB X chromosome. |
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Term
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Definition
Using mutations to study the function of genes. |
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Term
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Definition
The first chemical to be shown to be mutagenic. |
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Term
Charlott Auerbach and colleagues |
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Definition
Discovered the mutagenic effects of mustard gas. They were unable to do experiments with it because the gas was classified in WWII. |
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Term
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Definition
A mutagenic agent that is incorporated into DNA in the place of bases during replication. Their structure is similar to bases but with an increase frequency of mispairing. Includes 5-bromouracil. |
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Term
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Definition
A thymine base analog. It has a bromine group at the 5 position rather than a methyl group. It has increased frequency of tautomeric shifts. In keto form it pairs with A. In enol form it pairs with G. |
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Term
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Definition
A mutagenic agent. Acts on replicating or non-replicating DNA. Cytosine turns to uracil. Adenine turns to hypoxanthine. Guanine turns to xanthine.
This mutagen can effect the base-pairs twice, cancelling itself out. |
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Term
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Definition
What adenine turns into when exposed to nitrous acid. It pairs with cytosine, resulting in mutation. |
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Term
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Definition
What guanine turns into when exposed to nitrous acid. It pairs with cytosine, so there is no mutation. |
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Term
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Definition
A mutagenic agent that donates an alkyl. It is mutagenic to replicating and non-replicating DNA. Induce transitions, transversions, frameshift mutations, and chromosome aberrations. |
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Term
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Definition
A mutagenic agent that induces only G:C -> A:T transition. Cytosine turns into hydroxylamine, which pairs with T.
This is often used to classify transition mutations. |
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Term
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Definition
High-energy radiationi such as X ray, gamma ray, and cosmic rays. It collides with atoms, creaing free radicals or ions. It is measured in r. |
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Term
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Definition
The units used to to measure doses of ionizing radiation. It has a positive correlation with mutation. Chromic doses have less mutations than acute doses. Intermittent doses have less mutations. |
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Term
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Definition
Low-energy radiation. Penetrates only the surface layer of large organisms. Can be lethal to single-celled organisms. Includes UV rays. |
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Term
Ultraviolet (UV) Radiation |
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Definition
A non-ionizing radiation. I is readily absorbed by DNA, causing base hydrates or dimers that mess up DNA structure and cause mutations. |
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Term
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Definition
A gene that can move from one site to another. This often renders the gene non-functional. |
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Term
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Definition
Is a repeated sequence from 1 to 6 nucleotidess long. |
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Term
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Definition
A simple tandem repeat that is 3 nucleotides long. It is responsible for many diseases in humans including Fragile X syndrome. It has anticipation. The longer the repetition, the more severe the symptoms. |
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Term
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Definition
A disease caused by a trinucleotide repeat. CGG is repeated in the X chromosome. A normal person has 6 to 50 repeats. Fragile X may have up to 1000 repeats. |
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Term
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Definition
When in a trinucleotide repeat each generation of carriers has a longer repetition segment, and such has more severe symptoms and earlier onset. |
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Term
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Definition
Rare chemical fluctuations in DNA base pairs. Enol and imino forms of the base pairs. It can cause errors in DNA replication, due to mispairing. |
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Term
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Definition
Causes a hairpin to form in the DNA. |
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Term
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Definition
A single base mutation that causes no change in protein expression. |
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Term
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Definition
A single base mutation that causes a start or stop codon. This can be bad if it is near the start of the RNA. |
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Term
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Definition
A single base mutation that causes an amino acid of similar properties to be expressed. May not alter the function of the protein. |
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Term
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Definition
A single base mutation that caues a amino acid of diffferent properties to be expressed. Alters the function of the protein. |
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Term
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Definition
CTP repeat in the untranslated region of mRNA, encoding for kinase enzyme. Or a CCTG repeat in an intron on a zinc finger gene. Not on a coding region, but makes the mRNA too large for export into the cytoplasm. |
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Term
Incomplete / Partial Dominance |
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Definition
When a heterozygote has a different phenotype from either homozygote. |
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Term
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Definition
When a heterozygote has a phenotype that is a mix of the two alleles. Example: snapdragons heterozygote for red and white alleles show pink flowers. |
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Term
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Definition
When a heterozygote shows both traits simultaneously. Example: blood type AB shows both A and B blood type at the same time. |
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Term
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Definition
When there are more than two alleles for a gene. Denoted by a superscript. The allelic series can be worked out experimentally. Example: rabbit coats. |
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Term
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Definition
The most common allele in a wild population. Denoted by "+". |
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Term
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Definition
A mutant allele that is recessive. You can use a complementation test to determine what gene the new allele is on.
They include loss-of-function mutations. |
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Term
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Definition
A test to determine what allele a mutation is on. Breed mutant with known recessive mutants of various genes, and observe the phenotypes: the parent of the offspring showing mutant phenotypes is mutant on the correct gene. This only works for recessive mutations, never dominant mutations. |
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Term
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Definition
An allele that fails to do a function, such as the albino allele, which fails to produce pigment. |
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Term
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Definition
An allele that does a function partially, such as the chinchilla allele in rabbits; only makes enough pigment for the tips of hair. |
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Term
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Definition
A mutation that causes a visible, observable trait. Usually they are recessive. |
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Term
Loss-of-function mutation |
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Definition
A mutation that causes a protein to be under-functional, non-functional, or absent. Includes null and hypomorphic alleles.
If the mutation is recessive, a heterozygote will show wild-type phenotype, since the other chromosome is present, providing the missing protien.
If the mutation is dominant, gene shows haploinsufficiency. |
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Term
Temperature-sensitive mutation |
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Definition
A mutation that shows its phenotype based on temperature. Example: himalayan mutation in cats and rabbits. Pigment only present in relatively cold extremeties. |
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Term
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Definition
A mutation that is dominant. Includes dominant-negative mutations, and gain-of-function mutations. |
|
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Term
Dominant-negative mutation |
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Definition
A dominant mutation that inhibits protein production, creating a mutant phenotype that is present in a heterozygote. Includes MITP. |
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Term
Gain-of-function mutation |
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Definition
A dominant mutation that enhances an existing protein, creates a new protein, or produces the protein in a different place or time. Example: antennapedia. |
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Term
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Definition
An allele found at appreciable frequencies at least above 1%, but is not the wild-type. |
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Term
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Definition
When a the amount of protein present effects phenotype, and a heterozygous shows mutant phenotype because of this. Causes a dominant loss-of-funciton allele. |
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Term
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Definition
When there are multiple alleles, it is necessary to work out what alleles are most dominant, and which are most recessive. Experimentally you work out an order of dominance hierarchy. |
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Term
MIcrophthalmia protein (MITP) |
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Definition
A dominant-negative mutation where two wild-type proteins are translated together, and thus are stuck together at the end. Causes both proteins to be fully or partially non-functional. |
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Term
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Definition
A gain-of-function mutation in fruit flies causing legs to grow in the place of antennae. |
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Term
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Definition
"Paralysis" in Japanese. A mutation in fruit flies that is activated at elevated temperatures. The flies become paralyzed. |
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Term
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Definition
A mutation in humans effecting the metabolism of phenylalanine. Infants with PKU must be put on a low-phenylalanine diet or toxins will build up in their brains, impairing brain development and ability.
PKU has pleiotropy. People with PKU have light brown or blonde hair, and their urine contans rare compounds. |
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Term
|
Definition
A allel in humans that is expressed differently in males and females. In males it is dominant and will show in heterozygotes. In females it is recessive and will show only in homozygotes, and when it does, the phenotype is lessened to hair thinning rather than balding. The allele interacts with testosterone. |
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Term
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Definition
When an individual should show a phenotype according to their genotype, but for some reason they do not. This can cause incorrect genotyping by genetic counselors. |
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Term
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Definition
A mutation in humans where there are extra fingers and/or toes. A dominant gain-of-funcion mutation, however there is sometimes incomplete penetrance. |
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Term
|
Definition
When a trait doesn't show uniformly among individuals with the same genotype. Other factors, like environment or other genes cause a range of phenotypes. Sometimes the phenotype is completely absent like in incomplete penetrance. |
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Term
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Definition
A mutation in fruit flies that has variable expressivity. The phenotype can vary from normal, to smaller deformed eyes, to complete absence of eyes (and anything in between). |
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Term
|
Definition
"Stand above" in Greek. When there are two genes for a trait, but an allele of one of them has an overriding effect on the phenotype. |
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Term
|
Definition
"To make many turns" in Greek. When one gene affects several aspects of the phenotype. |
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Term
|
Definition
Alleles that only express their phenotypes when there is a specific environmental condition, such as temperature, diet, gender, or other genes. |
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Term
|
Definition
When different combinations of alleles in two genes produce different phenotypes. Example: chicken comb shape. |
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Term
|
Definition
When two genes have the same function. If one is lost due to mutation, the other one can pick up its task, producing no change in phenotype. Only if both are lost is there a mutant phenotype. |
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Term
|
Definition
A mutation in humans causing the absence of an enzyme. It is only active if the individual eats fava beans or takes anti-malaria drugs. |
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Term
Special / Regulatory transcription factor |
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Definition
Transcription factors that bind to enhancers and interact with basal transcription factors and RNA polymerase. |
|
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Term
|
Definition
A DNA sequence in the vicinity of the genes they effect. May be upstream, downstream, or in an intron. Doesn't mater what their orientation in the DNA is. Special transcription factors bind to them. They have effect on gene expression due to mediator complexes. |
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Term
Pamela Geyer and Victor Corces |
|
Definition
Showed that the yellow gene in fruit flies is regulated by several enhancers, some of which are on introns. They activate transcription in different body parts of the fly. |
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Term
|
Definition
A complex that bends DNA in such a way that proteins bound to enhancers are next to proteins bound to promoters. This is how enhancers have control over gene expression. |
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Term
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Definition
The nucleus from Dorset sheep mammary cell was transfered into a sheep's egg cell. The egg was then placed in the womb of a Scottish blackface sheep. The lamb developed normally into a Dorset sheep the exact clone of the mammary cell donor sheep (Scottish blackface surrogate used to prove it was not a normal pregnancy). This is proof against gene loss theory of differentiation: the mammary cell had all the information necessary to produce a complete sheep. |
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Term
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Definition
An enhancer sequence in mice that is a million base pairs away from the gene it effects. It enhances limbs in mice. |
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