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Transcription

Transcription makes RNA from DNA. RNA is used directly or indirectly to make chemical machines.

The
starting point for the transcription must be found. The DNA must be transcribed into a chain of many types of RNA, and transcription must stop at the correct point. In eucaryotes, the RNA must be capped and tailed so that the RNA can be sent through the nucleus, and so that it can be read for translation. In eucaryotes, the introns must also be spliced out.

Transcription Initiation

In bacterial transcription, the
sigma factor protein binds to the RNA polymerase. This helps the polymerase bind and find the promoter consensus sequence. A promoter may be the starting point of many genes for bacteria, but only one in eucaryotes.

Eucaryotes require many general transcription factors to get started, and there is also a TATA box, that is encoded into the promoter, and found by a general transcription factor. There is also an activator protein that finds an enhancer site. This helps to regulate gene expresion. The mediator helps to bind the activator, and polymerase to help bind to the DNA. Eucaryotes also have a chromatin remodeling complex, and a histone acetylase protein to help separate the chromatin. There are also capping and tailing enzymes loaded onto the phosphorylated tail of the polymerase.

Transcription Elongation

In bacterial transcription, after ten or so nucleotides are complementarily bound, the sigma factor releases, and the polymerase moves more rapidly. The polymerase opens the DNA in an easily reversible state, so that the DNA can bind back together. A rudder like structure on the polymerase separates the DNA from the newly made RNA. There are also elongation proteins that help the polymerase stay bound to the DNA.

Transcription Termination

In bacteria and eucaryotes, there is a terminator sequence that allows the polymerase to dissassociate from the DNA. For many bacteria, the termination sequence has a string of A-T pairs, that self bind, and makes a hairpin.

Capping

In eucaryotes, a guanine cap is placed onto the 5' end of the RNA. This is performed shorty after initiation.

Tailing

In eucaryotes, a poly-A tail is placed onto the 3' end of the RNA. It reads a sequence from the DNA that indicates when to perform polyadenylation (put on the poly-A tail).

The cap and tail help identify this as an mRNA molecule so that it can be exported from the nucleus and used for translation.

Splicing

In eucaryotes, splicing must be performed to remove introns. Introns allow for rearranging genes in many ways and are only in eucaryotes. Splicing is performed during elongation. The branch point site is recognized by the branch point binding protein, and other proteins. The 5' splice site of the intron is cleaved and bound to the branch point. This forms the intron into a lariat, and then the lariat is cleaved at the 3' splice site, and the 5' and 3' splice sites are bound together.
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