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In transcription, what structural changes indicate the transition from initiation to elongation

In transcription, what structural changes indicate the transition from initiation to elongation
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In transcription, the structural changes indicate the transition from initiation to elongation are as follows:

Transcription is the first step in gene expression and is the major target of reulation.

-Can be divided into three distinct phases i.e. Initiation,elongation and termination.

structural changes indicate the transition from initiation to elongation in bacteria =

- In eubacterial species,transcription of all genes is mediated by a core RNAP complex,typically a 5-subunit (\alpha2\beta \beta'\omega ) enzyme.

-However,in order to recognize promoter DNA sequences ,this core enzyme must associate with a sigma factor to form RNAP holoenzyme.

-Initiation occurs at a site that is fixed distance from the \sigma recognition sequences.

-Eubacterial species typically contain multiple \sigma factors that form distinct classes of RNAP holoenzymes that recognise different promoters sequences and reguate distinct classes of genes.

-steps in transcription initiation are

1.preinitiation closed complex formation at the promoter by RNAP holoenzyme,containing \sigma factor.

2.DNA is unwound around the transcription start site to form an open complex.

3.Abortive synthesis of 2-15 nt RNAs requiring DNA "scrunching".

4.Promoter escape istypically associated with loss of \sigma factor.

structural changes indicate the transition from initiation to elongation in eukaryotes =

-Eukaryotic cells contain 3 nuclear RNA polymerases,with RNA polymerase II (polII) responsible for transcribing all mRNAs and numerous non-coding RNAs.

-Pol II ,a 12 subunit enzyme with many similarities to bacterial RNAP,does not recognize promoter DNA by itself,but rather a part of the basal pol II machinary that includes general transcription factors i.e.TFIIA,B,C,D.E.F,H.

-These factors do not associate with elongating Pol II,and hence rapidly dissociate from Pol II during the transition between initiation and elongation.

- number of factors e.g.FACT,Spt 4,Paf 1 and TREX complexes,Spt6,travel with elongating Pol II throughout the coding region.

- Eukaryotic Pol II must contend with nucleosomes that inhibit both initiation and elongation.

- Open complex formation requires the helicase activity of TFIIH,and promoter escapes does not coincide with abortive initiation.

-Escape from promoter-proximal pauses is associated with phosphorylation at serine 2 of the C-terminal domain of the largest Pol II subunit by TEFb.

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