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-study of the variability and transmission of characteristics -study of genes, how they carry and pass information |
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all genetic information in a cell including chromosomes and plasmids |
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structure containing DNA that physically carry hereditary information |
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self replicating, gene containing circular piece of DNA |
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genetic constitution of the cell, organism, or individual |
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-observable characteristic -results from expression of genes and environmental factors |
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-circular molecule of DNA -looped and folded -attached to plasma membrane at one or more points -about 1 mm long -supercoiled (10% of cell volume) |
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-genetic info is used within a cell to produce proteins needed for the cell to function |
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transfer of genetic information between the same generation of cells |
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overview of DNA replication (1-5) |
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-one parental ds DNA is converted into 2 ds daughter DNA molecules -one stand acts as a template for the other -Gyrase/Topoisomerase relaxes supercoiling -Helicase unwinds the two parental strands like a zipper -replication fork is the point where replication occurs |
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overview of DNA replication (6-10) |
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-DNA polymerase synthesizes a new DNA strand 5' to 3' -the leading strand is oriented 5' to 3' in which a polymerase "reads" the DNA and adds nucleotides continuously -lagging strand is oriented 3' to 5' in which primase "reads" the DNA and adds RNA in short seperated fragements(Okazaki) -primers are removed -DNA ligase joins fragments together |
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bacterial DNA replication is... |
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at completion of bacterial DNA replication, both forks meet and are separated by |
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1 mistake in DNA rep every ____ due to proofreading of_______ |
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10^10 bases DNA polymerase |
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-synthesis of a complementary strand of RNA (mRNA) from DNA -RNA polymerase binds to a promotor on the DNA and initiates transcription -only one of the two DNA strands acts as a template -RNA is synthesize 5' to 3' -transcription stops once RNA polymerase reaches the terminator |
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-protein synthsis -decoding of nucleotides into amino acids -the sequence of codons (3 nucleotides) on an mRNA molecule determines the sequence of amino acids in the protein |
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in prokaryotes transcription/translation |
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-simultaneous -translation can begin before transcription is complete -occur in cytoplasm -start codon is available to ribsomes |
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eukaryotes transcription/translation |
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-transciption occurs in nucleus and must be completed before it is sent to cytoplasm -presence of noncoding DNA(introns) between expressed DNA regions (extrons) -introns removed and extrons spliced together |
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remove introns and splice extrons |
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regulation of bacterial gene expression |
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-most genes (60-80%) are always turned on /expressed constitutively(enzymes of glycolysis) -expression of other genes is regulated/only expressed when needed (catabolic enzymes/surface proteins) |
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-mechanisms that inhibits gene expression and decrease synthesis of enzymes usually in response to an excess of surplus |
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-regulatory proteins that block the ability of RNA polymerase to initiate transcription |
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-mechanisms responsible for turning on the expression of a gene |
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substances that induce the transcription of genes |
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-genes coding for 3 enzymes involved in lactose uptake and utilization are next to eachother -LacZ, LacY, LacA (structural genes) |
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region on DNA where RNA polymerase initiates transcription |
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-segment of DNA that a repressor or activator binds to |
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regulatory gene that codes for a repressor protein |
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change in the base sequence of DNA |
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-protein misfolded -enzyme less activated/inactivated |
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-occurs when mutated base is on the 3rd position of the mRNA codon -codes for same amino acid or has same properties (Asp-Glu) |
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point mutation/base substitution |
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- a single base is replaced with another base -transition-purine for purine or vv -transversion-purine for pyramidine or vv |
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base substitution results in a different amino acid |
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base substitution results in a STOP codon |
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spontaneous or induced by physical or chemical agents |
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-nitrous acid -UV light -radiation -nucleoside analogs |
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probability that a gene will mutate when a cell divides |
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spontaneous mutation rate |
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mutagens increase mutation rate |
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why bacteria used to study mutation |
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-divide rapidly -only one copy of each gene per cell |
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-selection that kills unmutated cells |
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-used to identify mutants that have lost ability to synthesize an amino acid -these mutant cells cannot grow in the absence of that amino acid (auxotroph) |
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replica plating technique |
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-using a velvet to transfer colonies to histidine and non histadine plates to identify auxotrophs |
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-exchange of genes between 2 DNA molecules |
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protein that catalyzes the joining of 2 stands or recom DNA |
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mechanisms of Recombination |
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-transformation -conjugation -transduction |
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-genes transferred from one bacterium to another as naked DNA -no contact necessary between donor and recipient -could happen naturally or be induced |
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mechanism of transformation |
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-DNA fragments bind to exterior of cell -fragmentation of DNA -one DNA is transferred up to cytoplasm, other is degraded |
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-transfer a portion of a donor bacterium chromosome to a recipient -requires direct contact -as the donor replicates its chromosome, the copy is injected into the recipient -only can occur between cells of opposite mating types |
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-donor that carries fertility factor (lack Bio- and Met-) -recipient that does not (lacks Thr- and Leu) |
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set of genes originally acquired from a plasmid and now integrated into the bacterial chromosome -established the origin of replication for the chromosome |
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-transfer of bacterial DNA through a virus (bacteriophage) |
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-fertility -resistance -col-plasmids -degradative -virulence |
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-contain genes that can build resistance against antibiotics or poisons |
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contain genes that code for bacteriocins (proteinacious toxins) |
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allow degradation of unusual substance (toluene) |
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turn bacterium into a pathogen |
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small segments of DNA that can be moved from one region of DNA to another (often within genes) |
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