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An aromatic residue switch in enhancer-dependent bacterial RNA polymerase controls transcription intermediate complex activity
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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3675486/ https://www.ncbi.nlm.nih.gov/pubmed/23609536 http://dx.doi.org/10.1093/nar/gkt271 |
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author | Wiesler, Simone C. Weinzierl, Robert O. J. Buck, Martin |
author_facet | Wiesler, Simone C. Weinzierl, Robert O. J. Buck, Martin |
author_sort | Wiesler, Simone C. |
collection | PubMed |
description | 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 σ-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 σ(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. |
format | Online Article Text |
id | pubmed-3675486 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-36754862013-06-07 An aromatic residue switch in enhancer-dependent bacterial RNA polymerase controls transcription intermediate complex activity Wiesler, Simone C. Weinzierl, Robert O. J. Buck, Martin Nucleic Acids Res Nucleic Acid Enzymes 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 σ-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 σ(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. Oxford University Press 2013-06 2013-04-22 /pmc/articles/PMC3675486/ /pubmed/23609536 http://dx.doi.org/10.1093/nar/gkt271 Text en © The Author(s) 2013. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Nucleic Acid Enzymes Wiesler, Simone C. Weinzierl, Robert O. J. Buck, Martin An aromatic residue switch in enhancer-dependent bacterial RNA polymerase controls transcription intermediate complex activity |
title | An aromatic residue switch in enhancer-dependent bacterial RNA polymerase controls transcription intermediate complex activity |
title_full | An aromatic residue switch in enhancer-dependent bacterial RNA polymerase controls transcription intermediate complex activity |
title_fullStr | An aromatic residue switch in enhancer-dependent bacterial RNA polymerase controls transcription intermediate complex activity |
title_full_unstemmed | An aromatic residue switch in enhancer-dependent bacterial RNA polymerase controls transcription intermediate complex activity |
title_short | An aromatic residue switch in enhancer-dependent bacterial RNA polymerase controls transcription intermediate complex activity |
title_sort | aromatic residue switch in enhancer-dependent bacterial rna polymerase controls transcription intermediate complex activity |
topic | Nucleic Acid Enzymes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3675486/ https://www.ncbi.nlm.nih.gov/pubmed/23609536 http://dx.doi.org/10.1093/nar/gkt271 |
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