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Transcription has some proofreading mechanisms, but they are fewer and less effective than the controls for DNA; therefore, transcription has a lower copying fidelity than DNA Replication . Like DNA Replication , transcription proceeds in the 5' → 3' direction (ie the old polymer is read in the 3' → 5' direction and the new, complementary fragments are generated in the 5' → 3' direction). Transcription is divided into 3 stages: ''initiation'', ''elongation'' and ''termination''. PROKARYOTIC TRANSCRIPTION
Initiation The following steps occur, in order, for transcription initiation:
Promoters can differ in "strength"; that is, how actively they promote transcription of their adjacent DNA sequence. Promoter strength is in many (but not all) cases, a matter of how tightly RNA polymerase and its associated accessory proteins bind to their respective DNA sequences. The more similar the sequences are to a Consensus Sequence , the stronger the binding is. Most transcripts originate using adenosine-5'-triphosphate ( ATP ) and, to a lesser extent, guanosine-5'-triphosphate ( GTP ) ( Purine nucleoside triphosphates) at the +1 site. Uridine-5'-triphosphate ( UTP ) and cytidine-5'-triphosphate (CTP) ( Pyrimidine nucleoside triphosphates) are disfavoured at the initiation site. Termination Two termination mechanisms are well known:
Other termination mechanisms include where RNAP comes across a region with repetitious thymidine residues in the DNA template. or where a GC-rich inverted repeat followed by 4 A residues. the inverted repeat forms a stable stem loop structure in the Rna, which causes the RNA to dissociate from the DNA template. |
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