Imperial College London

DrRobertWeinzierl

Faculty of Natural SciencesDepartment of Life Sciences

Reader in Molecular Biology
 
 
 
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Contact

 

+44 (0)20 7594 5236r.weinzierl

 
 
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Location

 

510Sir Alexander Fleming BuildingSouth Kensington Campus

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Summary

 

Publications

Citation

BibTex format

@article{Wiesler:2013:nar/gkt271,
author = {Wiesler, SC and Weinzierl, RO and Buck, M},
doi = {nar/gkt271},
journal = {Nucleic Acids Res},
title = {An aromatic residue switch in enhancer-dependent bacterial RNA polymerase controls transcription intermediate complex activity},
url = {http://dx.doi.org/10.1093/nar/gkt271},
year = {2013}
}

RIS format (EndNote, RefMan)

TY  - JOUR
AB - 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 sigma54-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.
AU - Wiesler,SC
AU - Weinzierl,RO
AU - Buck,M
DO - nar/gkt271
PY - 2013///
SN - 1362-4962
TI - An aromatic residue switch in enhancer-dependent bacterial RNA polymerase controls transcription intermediate complex activity
T2 - Nucleic Acids Res
UR - http://dx.doi.org/10.1093/nar/gkt271
UR - http://www.ncbi.nlm.nih.gov/pubmed/23609536
ER -