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Na(+) riboswitches regulate genes for diverse physiological processes in bacteria

Organisms presumably have mechanisms to monitor and physiologically adapt to changes in cellular Na(+) concentrations. Only a single bacterial protein has previously been demonstrated to selectively sense Na(+) and regulate gene expression. Here we report a riboswitch class, previously called the ‘D...

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Autores principales: White, Neil, Sadeeshkumar, Harini, Sun, Anna, Sudarsan, Narasimhan, Breaker, Ronald R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9337991/
https://www.ncbi.nlm.nih.gov/pubmed/35879547
http://dx.doi.org/10.1038/s41589-022-01086-4
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author White, Neil
Sadeeshkumar, Harini
Sun, Anna
Sudarsan, Narasimhan
Breaker, Ronald R.
author_facet White, Neil
Sadeeshkumar, Harini
Sun, Anna
Sudarsan, Narasimhan
Breaker, Ronald R.
author_sort White, Neil
collection PubMed
description Organisms presumably have mechanisms to monitor and physiologically adapt to changes in cellular Na(+) concentrations. Only a single bacterial protein has previously been demonstrated to selectively sense Na(+) and regulate gene expression. Here we report a riboswitch class, previously called the ‘DUF1646 motif’, whose members selectively sense Na(+) and regulate the expression of genes relevant to sodium biology. Many proteins encoded by Na(+)-riboswitch-regulated genes are annotated as metal ion transporters, whereas others are involved in mitigating osmotic stress or harnessing Na(+) gradients for ATP production. Na(+) riboswitches exhibit dissociation constants in the low mM range, and strongly reject all other alkali and alkaline earth ions. Likewise, only Na(+) triggers riboswitch-mediated transcription and gene expression changes. These findings reveal that some bacteria use Na(+) riboswitches to monitor, adjust and exploit Na(+) concentrations and gradients, and in some instances collaborate with c-di-AMP riboswitches to coordinate gene expression during osmotic stress. [Image: see text]
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spelling pubmed-93379912022-07-31 Na(+) riboswitches regulate genes for diverse physiological processes in bacteria White, Neil Sadeeshkumar, Harini Sun, Anna Sudarsan, Narasimhan Breaker, Ronald R. Nat Chem Biol Article Organisms presumably have mechanisms to monitor and physiologically adapt to changes in cellular Na(+) concentrations. Only a single bacterial protein has previously been demonstrated to selectively sense Na(+) and regulate gene expression. Here we report a riboswitch class, previously called the ‘DUF1646 motif’, whose members selectively sense Na(+) and regulate the expression of genes relevant to sodium biology. Many proteins encoded by Na(+)-riboswitch-regulated genes are annotated as metal ion transporters, whereas others are involved in mitigating osmotic stress or harnessing Na(+) gradients for ATP production. Na(+) riboswitches exhibit dissociation constants in the low mM range, and strongly reject all other alkali and alkaline earth ions. Likewise, only Na(+) triggers riboswitch-mediated transcription and gene expression changes. These findings reveal that some bacteria use Na(+) riboswitches to monitor, adjust and exploit Na(+) concentrations and gradients, and in some instances collaborate with c-di-AMP riboswitches to coordinate gene expression during osmotic stress. [Image: see text] Nature Publishing Group US 2022-07-25 2022 /pmc/articles/PMC9337991/ /pubmed/35879547 http://dx.doi.org/10.1038/s41589-022-01086-4 Text en © The Author(s) 2022 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
White, Neil
Sadeeshkumar, Harini
Sun, Anna
Sudarsan, Narasimhan
Breaker, Ronald R.
Na(+) riboswitches regulate genes for diverse physiological processes in bacteria
title Na(+) riboswitches regulate genes for diverse physiological processes in bacteria
title_full Na(+) riboswitches regulate genes for diverse physiological processes in bacteria
title_fullStr Na(+) riboswitches regulate genes for diverse physiological processes in bacteria
title_full_unstemmed Na(+) riboswitches regulate genes for diverse physiological processes in bacteria
title_short Na(+) riboswitches regulate genes for diverse physiological processes in bacteria
title_sort na(+) riboswitches regulate genes for diverse physiological processes in bacteria
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9337991/
https://www.ncbi.nlm.nih.gov/pubmed/35879547
http://dx.doi.org/10.1038/s41589-022-01086-4
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