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The Csr system regulates genome-wide mRNA stability and transcription and thus gene expression in Escherichia coli
Bacterial adaptation requires large-scale regulation of gene expression. We have performed a genome-wide analysis of the Csr system, which regulates many important cellular functions. The Csr system is involved in post-transcriptional regulation, but a role in transcriptional regulation has also bee...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4844966/ https://www.ncbi.nlm.nih.gov/pubmed/27112822 http://dx.doi.org/10.1038/srep25057 |
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author | Esquerré, Thomas Bouvier, Marie Turlan, Catherine Carpousis, Agamemnon J. Girbal, Laurence Cocaign-Bousquet, Muriel |
author_facet | Esquerré, Thomas Bouvier, Marie Turlan, Catherine Carpousis, Agamemnon J. Girbal, Laurence Cocaign-Bousquet, Muriel |
author_sort | Esquerré, Thomas |
collection | PubMed |
description | Bacterial adaptation requires large-scale regulation of gene expression. We have performed a genome-wide analysis of the Csr system, which regulates many important cellular functions. The Csr system is involved in post-transcriptional regulation, but a role in transcriptional regulation has also been suggested. Two proteins, an RNA-binding protein CsrA and an atypical signaling protein CsrD, participate in the Csr system. Genome-wide transcript stabilities and levels were compared in wildtype E. coli (MG1655) and isogenic mutant strains deficient in CsrA or CsrD activity demonstrating for the first time that CsrA and CsrD are global negative and positive regulators of transcription, respectively. The role of CsrA in transcription regulation may be indirect due to the 4.6-fold increase in csrD mRNA concentration in the CsrA deficient strain. Transcriptional action of CsrA and CsrD on a few genes was validated by transcriptional fusions. In addition to an effect on transcription, CsrA stabilizes thousands of mRNAs. This is the first demonstration that CsrA is a global positive regulator of mRNA stability. For one hundred genes, we predict that direct control of mRNA stability by CsrA might contribute to metabolic adaptation by regulating expression of genes involved in carbon metabolism and transport independently of transcriptional regulation. |
format | Online Article Text |
id | pubmed-4844966 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48449662016-04-29 The Csr system regulates genome-wide mRNA stability and transcription and thus gene expression in Escherichia coli Esquerré, Thomas Bouvier, Marie Turlan, Catherine Carpousis, Agamemnon J. Girbal, Laurence Cocaign-Bousquet, Muriel Sci Rep Article Bacterial adaptation requires large-scale regulation of gene expression. We have performed a genome-wide analysis of the Csr system, which regulates many important cellular functions. The Csr system is involved in post-transcriptional regulation, but a role in transcriptional regulation has also been suggested. Two proteins, an RNA-binding protein CsrA and an atypical signaling protein CsrD, participate in the Csr system. Genome-wide transcript stabilities and levels were compared in wildtype E. coli (MG1655) and isogenic mutant strains deficient in CsrA or CsrD activity demonstrating for the first time that CsrA and CsrD are global negative and positive regulators of transcription, respectively. The role of CsrA in transcription regulation may be indirect due to the 4.6-fold increase in csrD mRNA concentration in the CsrA deficient strain. Transcriptional action of CsrA and CsrD on a few genes was validated by transcriptional fusions. In addition to an effect on transcription, CsrA stabilizes thousands of mRNAs. This is the first demonstration that CsrA is a global positive regulator of mRNA stability. For one hundred genes, we predict that direct control of mRNA stability by CsrA might contribute to metabolic adaptation by regulating expression of genes involved in carbon metabolism and transport independently of transcriptional regulation. Nature Publishing Group 2016-04-26 /pmc/articles/PMC4844966/ /pubmed/27112822 http://dx.doi.org/10.1038/srep25057 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Esquerré, Thomas Bouvier, Marie Turlan, Catherine Carpousis, Agamemnon J. Girbal, Laurence Cocaign-Bousquet, Muriel The Csr system regulates genome-wide mRNA stability and transcription and thus gene expression in Escherichia coli |
title | The Csr system regulates genome-wide mRNA stability and transcription and thus gene expression in Escherichia coli |
title_full | The Csr system regulates genome-wide mRNA stability and transcription and thus gene expression in Escherichia coli |
title_fullStr | The Csr system regulates genome-wide mRNA stability and transcription and thus gene expression in Escherichia coli |
title_full_unstemmed | The Csr system regulates genome-wide mRNA stability and transcription and thus gene expression in Escherichia coli |
title_short | The Csr system regulates genome-wide mRNA stability and transcription and thus gene expression in Escherichia coli |
title_sort | csr system regulates genome-wide mrna stability and transcription and thus gene expression in escherichia coli |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4844966/ https://www.ncbi.nlm.nih.gov/pubmed/27112822 http://dx.doi.org/10.1038/srep25057 |
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