4.8 Article

An aromatic residue switch in enhancer-dependent bacterial RNA polymerase controls transcription intermediate complex activity

期刊

NUCLEIC ACIDS RESEARCH
卷 41, 期 11, 页码 5874-5886

出版社

OXFORD UNIV PRESS
DOI: 10.1093/nar/gkt271

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资金

  1. Biotechnology and Biological Sciences Research Council [BB/H012249/1]
  2. Medical Research Council [G1100057]
  3. Imperial College London
  4. Biotechnology and Biological Sciences Research Council [BB/G001278/1, BB/H012249/1] Funding Source: researchfish
  5. Medical Research Council [G1100057] Funding Source: researchfish
  6. BBSRC [BB/H012249/1, BB/G001278/1] Funding Source: UKRI
  7. MRC [G1100057] Funding Source: UKRI

向作者/读者索取更多资源

The formation of the open promoter complex (RPo) in which the melted DNA containing the transcription start site is located at the RNA polymerase (RNAP) catalytic centre is an obligatory step in the transcription of DNA into RNA catalyzed by RNAP. In the RPo, an extensive network of interactions is established between DNA, RNAP and the Sigma-factor and the formation of functional RPo occurs via a series of transcriptional intermediates (collectively 'RPi'). A single tryptophan is ideally positioned to directly engage with the flipped out base of the non-template strand at the +1 site. Evidence suggests that this tryptophan (i) is involved in either forward translocation or DNA scrunching and (ii) in Sigma(54)-regulated promoters limits the transcription activity of at least one intermediate complex (RPi) before the formation of a fully functional RPo. Limiting RPi activity may be important in preventing the premature synthesis of abortive transcripts, suggesting its involvement in a general mechanism driving the RPi to RPo transition for transcription initiation.

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