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A conserved RNA seed‐pairing domain directs small RNA‐mediated stress resistance in enterobacteria
Small regulatory RNAs (sRNAs) are crucial components of many stress response systems. The envelope stress response (ESR) of Gram‐negative bacteria is a paradigm for sRNA‐mediated stress management and involves, among other factors, the alternative sigma factor E (σ(E)) and one or more sRNAs. In this...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6694218/ https://www.ncbi.nlm.nih.gov/pubmed/31313835 http://dx.doi.org/10.15252/embj.2019101650 |
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author | Peschek, Nikolai Hoyos, Mona Herzog, Roman Förstner, Konrad U Papenfort, Kai |
author_facet | Peschek, Nikolai Hoyos, Mona Herzog, Roman Förstner, Konrad U Papenfort, Kai |
author_sort | Peschek, Nikolai |
collection | PubMed |
description | Small regulatory RNAs (sRNAs) are crucial components of many stress response systems. The envelope stress response (ESR) of Gram‐negative bacteria is a paradigm for sRNA‐mediated stress management and involves, among other factors, the alternative sigma factor E (σ(E)) and one or more sRNAs. In this study, we identified the MicV sRNA as a new member of the σ(E) regulon in Vibrio cholerae. We show that MicV acts redundantly with another sRNA, VrrA, and that both sRNAs share a conserved seed‐pairing domain allowing them to regulate multiple target mRNAs. V. cholerae lacking σ(E) displayed increased sensitivity toward antimicrobials, and over‐expression of either of the sRNAs suppressed this phenotype. Laboratory selection experiments using a library of synthetic sRNA regulators revealed that the seed‐pairing domain of σ(E)‐dependent sRNAs is strongly enriched among sRNAs identified under membrane‐damaging conditions and that repression of OmpA is crucial for sRNA‐mediated stress relief. Together, our work shows that MicV and VrrA act as global regulators in the ESR of V. cholerae and provides evidence that bacterial sRNAs can be functionally annotated by their seed‐pairing sequences. |
format | Online Article Text |
id | pubmed-6694218 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-66942182019-08-19 A conserved RNA seed‐pairing domain directs small RNA‐mediated stress resistance in enterobacteria Peschek, Nikolai Hoyos, Mona Herzog, Roman Förstner, Konrad U Papenfort, Kai EMBO J Articles Small regulatory RNAs (sRNAs) are crucial components of many stress response systems. The envelope stress response (ESR) of Gram‐negative bacteria is a paradigm for sRNA‐mediated stress management and involves, among other factors, the alternative sigma factor E (σ(E)) and one or more sRNAs. In this study, we identified the MicV sRNA as a new member of the σ(E) regulon in Vibrio cholerae. We show that MicV acts redundantly with another sRNA, VrrA, and that both sRNAs share a conserved seed‐pairing domain allowing them to regulate multiple target mRNAs. V. cholerae lacking σ(E) displayed increased sensitivity toward antimicrobials, and over‐expression of either of the sRNAs suppressed this phenotype. Laboratory selection experiments using a library of synthetic sRNA regulators revealed that the seed‐pairing domain of σ(E)‐dependent sRNAs is strongly enriched among sRNAs identified under membrane‐damaging conditions and that repression of OmpA is crucial for sRNA‐mediated stress relief. Together, our work shows that MicV and VrrA act as global regulators in the ESR of V. cholerae and provides evidence that bacterial sRNAs can be functionally annotated by their seed‐pairing sequences. John Wiley and Sons Inc. 2019-07-17 2019-08-15 /pmc/articles/PMC6694218/ /pubmed/31313835 http://dx.doi.org/10.15252/embj.2019101650 Text en © 2019 The Authors. Published under the terms of the CC BY NC ND 4.0 license This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Articles Peschek, Nikolai Hoyos, Mona Herzog, Roman Förstner, Konrad U Papenfort, Kai A conserved RNA seed‐pairing domain directs small RNA‐mediated stress resistance in enterobacteria |
title | A conserved RNA seed‐pairing domain directs small RNA‐mediated stress resistance in enterobacteria |
title_full | A conserved RNA seed‐pairing domain directs small RNA‐mediated stress resistance in enterobacteria |
title_fullStr | A conserved RNA seed‐pairing domain directs small RNA‐mediated stress resistance in enterobacteria |
title_full_unstemmed | A conserved RNA seed‐pairing domain directs small RNA‐mediated stress resistance in enterobacteria |
title_short | A conserved RNA seed‐pairing domain directs small RNA‐mediated stress resistance in enterobacteria |
title_sort | conserved rna seed‐pairing domain directs small rna‐mediated stress resistance in enterobacteria |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6694218/ https://www.ncbi.nlm.nih.gov/pubmed/31313835 http://dx.doi.org/10.15252/embj.2019101650 |
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