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-polymer of nucleoties joined by phosphodiester bonds -ribose sugar -free OH group on 2' - Carbon atom of ribose sugar -pyrimidine thymine replaced by uracil in RNA -Usually single stranded |
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carries coding instruction for polypeptide chains from DNA to ribosome (It is translated into a polypeptide) |
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used in the building of ribosomes : machinery for synthesizing proteins by translating mRNA |
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RNA molecues that carry amino acids to the growing polypeptide |
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small nuclear RNA (smRNA) |
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transcription of genes for mRNA, rRNA, an tRNA -large precursor mols ("primary transcripts") -must be processed in nucleus -functional mols for export to cytosol |
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small nucleolar RNA (smoRNA) |
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invilved in chemical modifications of ribisomal RNA's (rRNAs) & other RNA's |
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microRNA (miRNA) and small interfering RNA (siRNA) |
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tiny RNA mols that appear to regulate the expression of mRNA mols by RNA interference |
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inactivates one of the two X chromosomes in female vertebrates |
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3 Major components of Transcripton |
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1. dna template 2. substrate to build new RNA mol. 3. transcription apparatus (proteins necessary to catalyze synthesis of RNA) |
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- ss DNA of double helix - only one nucleotide strand of the 2 making up the DNA helix used for transcription = TRANSCRIPTION STRAND - RNA strand complementary and antiparalel to DNA template strand synthesized |
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A few nomenclature conventions: |
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- nontemplate strand - template strand - DNA - transcription - RNA Transcript - translation |
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~ identical to coding (non-template, sense) strand, except U's instead of T's
See slide 13 of lecture 14. |
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The RNA transcript has the same sequence as the... |
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RNA is synthesized in a _' to _' direction only.
The Template strand is read in the : |
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5' to 3'
3' to 5' direction |
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Which strand of DNA can be used as template strand for transcription? |
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The building blocks of transcription: |
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Ribonucleoside triphosphates (rNTP's) - the subunits!
- nucleotides added 1 at a time to 3'-OH group of RNA mol, in 5' to 3' direction. - 2 phosphates cleaved off rNTP & other 1 forms phosphodiester bond, no primer necessary. |
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Carries out the different types of transcriptions: |
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RNA polymerases are assisted by several other proteins: |
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transcriptions factors (TF), which join and leave RNA polymerases at different stages of transcription. Each provides a special function. |
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- usually only possesses single RNA polymerase |
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Pre-mRNA, some snRNAs, snoRNAs, some miRNAs |
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tRNAs, small rRNAs, some snRNAs, some miRNAs |
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stretch of DNA that encodes an RNA mol and sequences necessary for its transcription |
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DNA sequence that guide RNA Polymerase to the transcription start site |
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sequence of DNA copied to RNA mol |
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DNA sequence that specify termination of RNA synthesis, i.e. transcription & release of RNA Polymerase from DNA |
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- at 5' end of gene - binding of RNA polymerase to promoter - unwinding of DNA |
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- addition of nucleotides to 3' end (3'-OH) of growing chain - governed by rules of complementary base pairing - energy from NTP's |
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- at 3' end of gene - separation of RNA from DNA template - end-processing enzymes (for mRNA) |
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1. promoter recognition 2. formation of transcription bubble 3. addition of 1st nucloetides 4. escape of transcription apparatus from promoter |
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consists of the most commonly occuring bases at each position in a group of related sequences |
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Example of consensus sequence - a prokaryotic promoter (ON SLIDE 30 of lecture 14) |
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Transcription Factors (TF) |
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Proteins that are essential co-factors for Eukaryotic RNA polymerases.
RNA polymerase II cannot bind to "promoter" without aid of TFs --> involved in gene regulation |
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Generic; required by every gene for basal level gene expression (no transcription initiation without these). |
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Transcription Activation Factors TAFs (gene-specific) |
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regulate efficiency of expression (greatly enhance initiation of transcription). |
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25 to 35 bases upstream of initiation site; affects transcription rate and location of start site. In most pol II transcribed genes. |
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Francis Crick (1958): Refers only to protein coding sequence of gene and mRNA (exceptions to the rule in eukaryotes) |
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non-coding region; total intron length can exceed exon length and sizes vary. Introns are considered non critical. |
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The entire DNA sequence required to transcribe and encode a single RNA molecule. |
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A.) Cutting and trimming to generate end products: rRNA, tRNA, and mRNA. B.) Covalent Modification: Addition of cap and polyA tail to mRNA, addition of methyl group to 2'-OH of ribose in mRNA and rRNA, and extensive chemical changes of bases in tRNA. C.) Splicing; pre-rRNA, pre-mRNA, pre-tRNA by different mechanisms. |
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addition of 7-methylguanosine to the 5'end shortly after transcription begins. Protects 5'-end of mRNA. |
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addition of 100-250 adenine nucleotides to 3' end and downstream of AAUAAA; process = polyadenylation. |
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Intron removal by spliceosome |
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All introns have 5'-GU and AG-3' recognition sequence (GU-AG rule), small nuclear ribonucleoproteins (snRNPs) of spliceosome provide catalysis, and introns excised as lariat destroyed. |
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The elimination of particular regions from from the primary transcript in nucleus which results in a functional RNA (mRNA, tRNA, or rRNA). |
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Precise and strictly regulated biochemical process guided by specific sequences within the primary transcript and other RNA molecules within the "spliceosome" ribonucleoprotein (RNP) enzyme. |
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Found in bacteria only and is a 5' untranslated region before the start codon of mRNA. |
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a protein-RNA complex (spliceosome), responsible for pre-mRNA splicing. |
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Self splicing of catalytic RNA sequences (ribozymes). |
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