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Control of transcription elongation and DNA repair by alarmone ppGpp
Second messenger (p)ppGpp (collectively guanosine tetraphosphate and guanosine pentaphosphate) mediates bacterial adaptation to nutritional stress by modulating transcription initiation. More recently, ppGpp has been implicated in coupling transcription and DNA repair; however, the mechanism of ppGp...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group US
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10191844/ https://www.ncbi.nlm.nih.gov/pubmed/36997761 http://dx.doi.org/10.1038/s41594-023-00948-2 |
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author | Weaver, Jacob W. Proshkin, Sergey Duan, Wenqian Epshtein, Vitaly Gowder, Manjunath Bharati, Binod K. Afanaseva, Elena Mironov, Alexander Serganov, Alexander Nudler, Evgeny |
author_facet | Weaver, Jacob W. Proshkin, Sergey Duan, Wenqian Epshtein, Vitaly Gowder, Manjunath Bharati, Binod K. Afanaseva, Elena Mironov, Alexander Serganov, Alexander Nudler, Evgeny |
author_sort | Weaver, Jacob W. |
collection | PubMed |
description | Second messenger (p)ppGpp (collectively guanosine tetraphosphate and guanosine pentaphosphate) mediates bacterial adaptation to nutritional stress by modulating transcription initiation. More recently, ppGpp has been implicated in coupling transcription and DNA repair; however, the mechanism of ppGpp engagement remained elusive. Here we present structural, biochemical and genetic evidence that ppGpp controls Escherichia coli RNA polymerase (RNAP) during elongation via a specific site that is nonfunctional during initiation. Structure-guided mutagenesis renders the elongation (but not initiation) complex unresponsive to ppGpp and increases bacterial sensitivity to genotoxic agents and ultraviolet radiation. Thus, ppGpp binds RNAP at sites with distinct functions in initiation and elongation, with the latter being important for promoting DNA repair. Our data provide insights on the molecular mechanism of ppGpp-mediated adaptation during stress, and further highlight the intricate relationships between genome stability, stress responses and transcription. |
format | Online Article Text |
id | pubmed-10191844 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group US |
record_format | MEDLINE/PubMed |
spelling | pubmed-101918442023-05-19 Control of transcription elongation and DNA repair by alarmone ppGpp Weaver, Jacob W. Proshkin, Sergey Duan, Wenqian Epshtein, Vitaly Gowder, Manjunath Bharati, Binod K. Afanaseva, Elena Mironov, Alexander Serganov, Alexander Nudler, Evgeny Nat Struct Mol Biol Article Second messenger (p)ppGpp (collectively guanosine tetraphosphate and guanosine pentaphosphate) mediates bacterial adaptation to nutritional stress by modulating transcription initiation. More recently, ppGpp has been implicated in coupling transcription and DNA repair; however, the mechanism of ppGpp engagement remained elusive. Here we present structural, biochemical and genetic evidence that ppGpp controls Escherichia coli RNA polymerase (RNAP) during elongation via a specific site that is nonfunctional during initiation. Structure-guided mutagenesis renders the elongation (but not initiation) complex unresponsive to ppGpp and increases bacterial sensitivity to genotoxic agents and ultraviolet radiation. Thus, ppGpp binds RNAP at sites with distinct functions in initiation and elongation, with the latter being important for promoting DNA repair. Our data provide insights on the molecular mechanism of ppGpp-mediated adaptation during stress, and further highlight the intricate relationships between genome stability, stress responses and transcription. Nature Publishing Group US 2023-03-30 2023 /pmc/articles/PMC10191844/ /pubmed/36997761 http://dx.doi.org/10.1038/s41594-023-00948-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Weaver, Jacob W. Proshkin, Sergey Duan, Wenqian Epshtein, Vitaly Gowder, Manjunath Bharati, Binod K. Afanaseva, Elena Mironov, Alexander Serganov, Alexander Nudler, Evgeny Control of transcription elongation and DNA repair by alarmone ppGpp |
title | Control of transcription elongation and DNA repair by alarmone ppGpp |
title_full | Control of transcription elongation and DNA repair by alarmone ppGpp |
title_fullStr | Control of transcription elongation and DNA repair by alarmone ppGpp |
title_full_unstemmed | Control of transcription elongation and DNA repair by alarmone ppGpp |
title_short | Control of transcription elongation and DNA repair by alarmone ppGpp |
title_sort | control of transcription elongation and dna repair by alarmone ppgpp |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10191844/ https://www.ncbi.nlm.nih.gov/pubmed/36997761 http://dx.doi.org/10.1038/s41594-023-00948-2 |
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