Table of contents |
2 Eukaryotic transcription |
Bacterial transcription
A (simple) model for a bacterial gene to be transcribed looks like this :
upstream ~17 bp The gene to transcribe downstream 5'----------|-35|---------|-10|----------------------|T|------------3' 3'----------|-35|---------|-10|----------------------|T|------------5' | |---------------------> mRNAwhere the region between -35 and -10 base pairs is called promoter, and |T| stands for terminator. The DNA between promoter and terminator is copied to mRNA, which is then translated into protein.
Promoters can differ in strength, that is, how attractive they are for RNAP. The more similar they are to a consensus sequence, the stronger they are. The "ideal" promoter in E. coli looks like this:
5'----TTGACA---|17 bp|----TATAAT---|7bp|---|purines|----3'
Termination
The elongation stops if:
Eukaryotic transcription
Gene expression in eukaryotes is largely controlled by transcription via transcription factors. As eukaryotes are much more complex than prokaryotes, and have their genetic material stored in the nucleus, the transcription mechanisms are more complicated here. For example, eukaryotes have three RNA polymerases, in contrast to prokaryotes, which only have one.
Initiation
The core promoter of eukaryotic genes stretches from position -45 to 0. Additionally, there can be an upstream control element present at the -180 to -107 region, which can amplify the RNAP binding by a factor of up to 100. This UCE usually contains a TATA box, a highly conserved DNA sequence that reads
See also:
Elongation
Termination
A major difference between prokaryotic and eukaryotic transcription is that the latter have splicing of the primary transcript, modifying the mRNA created during transcription.