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Xenogeneic silencing strategies in bacteria are dictated by RNA polymerase promiscuity
Horizontal gene transfer facilitates dissemination of favourable traits among bacteria. However, foreign DNA can also reduce host fitness: incoming sequences with a higher AT content than the host genome can misdirect transcription. Xenogeneic silencing proteins counteract this by modulating RNA pol...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8894471/ https://www.ncbi.nlm.nih.gov/pubmed/35241653 http://dx.doi.org/10.1038/s41467-022-28747-1 |
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author | Forrest, David Warman, Emily A. Erkelens, Amanda M. Dame, Remus T. Grainger, David C. |
author_facet | Forrest, David Warman, Emily A. Erkelens, Amanda M. Dame, Remus T. Grainger, David C. |
author_sort | Forrest, David |
collection | PubMed |
description | Horizontal gene transfer facilitates dissemination of favourable traits among bacteria. However, foreign DNA can also reduce host fitness: incoming sequences with a higher AT content than the host genome can misdirect transcription. Xenogeneic silencing proteins counteract this by modulating RNA polymerase binding. In this work, we compare xenogeneic silencing strategies of two distantly related model organisms: Escherichia coli and Bacillus subtilis. In E. coli, silencing is mediated by the H-NS protein that binds extensively across horizontally acquired genes. This prevents spurious non-coding transcription, mostly intragenic in origin. By contrast, binding of the B. subtilis Rok protein is more targeted and mostly silences expression of functional mRNAs. The difference reflects contrasting transcriptional promiscuity in E. coli and B. subtilis, largely attributable to housekeeping RNA polymerase σ factors. Thus, whilst RNA polymerase specificity is key to the xenogeneic silencing strategy of B. subtilis, transcriptional promiscuity must be overcome to silence horizontally acquired DNA in E. coli. |
format | Online Article Text |
id | pubmed-8894471 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-88944712022-03-17 Xenogeneic silencing strategies in bacteria are dictated by RNA polymerase promiscuity Forrest, David Warman, Emily A. Erkelens, Amanda M. Dame, Remus T. Grainger, David C. Nat Commun Article Horizontal gene transfer facilitates dissemination of favourable traits among bacteria. However, foreign DNA can also reduce host fitness: incoming sequences with a higher AT content than the host genome can misdirect transcription. Xenogeneic silencing proteins counteract this by modulating RNA polymerase binding. In this work, we compare xenogeneic silencing strategies of two distantly related model organisms: Escherichia coli and Bacillus subtilis. In E. coli, silencing is mediated by the H-NS protein that binds extensively across horizontally acquired genes. This prevents spurious non-coding transcription, mostly intragenic in origin. By contrast, binding of the B. subtilis Rok protein is more targeted and mostly silences expression of functional mRNAs. The difference reflects contrasting transcriptional promiscuity in E. coli and B. subtilis, largely attributable to housekeeping RNA polymerase σ factors. Thus, whilst RNA polymerase specificity is key to the xenogeneic silencing strategy of B. subtilis, transcriptional promiscuity must be overcome to silence horizontally acquired DNA in E. coli. Nature Publishing Group UK 2022-03-03 /pmc/articles/PMC8894471/ /pubmed/35241653 http://dx.doi.org/10.1038/s41467-022-28747-1 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 Forrest, David Warman, Emily A. Erkelens, Amanda M. Dame, Remus T. Grainger, David C. Xenogeneic silencing strategies in bacteria are dictated by RNA polymerase promiscuity |
title | Xenogeneic silencing strategies in bacteria are dictated by RNA polymerase promiscuity |
title_full | Xenogeneic silencing strategies in bacteria are dictated by RNA polymerase promiscuity |
title_fullStr | Xenogeneic silencing strategies in bacteria are dictated by RNA polymerase promiscuity |
title_full_unstemmed | Xenogeneic silencing strategies in bacteria are dictated by RNA polymerase promiscuity |
title_short | Xenogeneic silencing strategies in bacteria are dictated by RNA polymerase promiscuity |
title_sort | xenogeneic silencing strategies in bacteria are dictated by rna polymerase promiscuity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8894471/ https://www.ncbi.nlm.nih.gov/pubmed/35241653 http://dx.doi.org/10.1038/s41467-022-28747-1 |
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