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Mechanisms of σ(54)-Dependent Transcription Initiation and Regulation

Cellular RNA polymerase is a multi-subunit macromolecular assembly responsible for gene transcription, a highly regulated process conserved from bacteria to humans. In bacteria, sigma factors are employed to mediate gene-specific expression in response to a variety of environmental conditions. The m...

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Detalles Bibliográficos
Autores principales: Danson, Amy E., Jovanovic, Milija, Buck, Martin, Zhang, Xiaodong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7057263/
https://www.ncbi.nlm.nih.gov/pubmed/31029702
http://dx.doi.org/10.1016/j.jmb.2019.04.022
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author Danson, Amy E.
Jovanovic, Milija
Buck, Martin
Zhang, Xiaodong
author_facet Danson, Amy E.
Jovanovic, Milija
Buck, Martin
Zhang, Xiaodong
author_sort Danson, Amy E.
collection PubMed
description Cellular RNA polymerase is a multi-subunit macromolecular assembly responsible for gene transcription, a highly regulated process conserved from bacteria to humans. In bacteria, sigma factors are employed to mediate gene-specific expression in response to a variety of environmental conditions. The major variant σ factor, σ(54), has a specific role in stress responses. Unlike σ(70)-dependent transcription, which often can spontaneously proceed to initiation, σ(54)-dependent transcription requires an additional ATPase protein for activation. As a result, structures of a number of distinct functional states during the dynamic process of transcription initiation have been captured using the σ(54) system with both x-ray crystallography and cryo electron microscopy, furthering our understanding of σ(54)-dependent transcription initiation and DNA opening. Comparisons with σ(70) and eukaryotic polymerases reveal unique and common features during transcription initiation.
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spelling pubmed-70572632020-03-11 Mechanisms of σ(54)-Dependent Transcription Initiation and Regulation Danson, Amy E. Jovanovic, Milija Buck, Martin Zhang, Xiaodong J Mol Biol Article Cellular RNA polymerase is a multi-subunit macromolecular assembly responsible for gene transcription, a highly regulated process conserved from bacteria to humans. In bacteria, sigma factors are employed to mediate gene-specific expression in response to a variety of environmental conditions. The major variant σ factor, σ(54), has a specific role in stress responses. Unlike σ(70)-dependent transcription, which often can spontaneously proceed to initiation, σ(54)-dependent transcription requires an additional ATPase protein for activation. As a result, structures of a number of distinct functional states during the dynamic process of transcription initiation have been captured using the σ(54) system with both x-ray crystallography and cryo electron microscopy, furthering our understanding of σ(54)-dependent transcription initiation and DNA opening. Comparisons with σ(70) and eukaryotic polymerases reveal unique and common features during transcription initiation. Elsevier 2019-09-20 /pmc/articles/PMC7057263/ /pubmed/31029702 http://dx.doi.org/10.1016/j.jmb.2019.04.022 Text en © 2019 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Danson, Amy E.
Jovanovic, Milija
Buck, Martin
Zhang, Xiaodong
Mechanisms of σ(54)-Dependent Transcription Initiation and Regulation
title Mechanisms of σ(54)-Dependent Transcription Initiation and Regulation
title_full Mechanisms of σ(54)-Dependent Transcription Initiation and Regulation
title_fullStr Mechanisms of σ(54)-Dependent Transcription Initiation and Regulation
title_full_unstemmed Mechanisms of σ(54)-Dependent Transcription Initiation and Regulation
title_short Mechanisms of σ(54)-Dependent Transcription Initiation and Regulation
title_sort mechanisms of σ(54)-dependent transcription initiation and regulation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7057263/
https://www.ncbi.nlm.nih.gov/pubmed/31029702
http://dx.doi.org/10.1016/j.jmb.2019.04.022
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