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The conserved mosaic prophage protein paratox inhibits the natural competence regulator ComR in Streptococcus
Horizontal gene transfer is an important means of bacterial evolution. This includes natural genetic transformation, where bacterial cells become “competent” and DNA is acquired from the extracellular environment. Natural competence in many species of Streptococcus, is regulated by quorum sensing vi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6224593/ https://www.ncbi.nlm.nih.gov/pubmed/30409983 http://dx.doi.org/10.1038/s41598-018-34816-7 |
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author | Mashburn-Warren, Lauren Goodman, Steven D. Federle, Michael J. Prehna, Gerd |
author_facet | Mashburn-Warren, Lauren Goodman, Steven D. Federle, Michael J. Prehna, Gerd |
author_sort | Mashburn-Warren, Lauren |
collection | PubMed |
description | Horizontal gene transfer is an important means of bacterial evolution. This includes natural genetic transformation, where bacterial cells become “competent” and DNA is acquired from the extracellular environment. Natural competence in many species of Streptococcus, is regulated by quorum sensing via the ComRS receptor-signal pair. The ComR-XIP (mature ComS peptide) complex induces expression of the alternative sigma factor SigX, which targets RNA polymerase to CIN-box promoters to activate genes involved in DNA uptake and recombination. In addition, the widely distributed Streptococcus prophage gene paratox (prx) also contains a CIN-box, and here we demonstrate it to be transcriptionally activated by XIP. In vitro experiments demonstrate that Prx binds ComR directly and prevents the ComR-XIP complex from interacting with DNA. Mutations of prx in vivo caused increased expression of the late competence gene ssb when induced with XIP as compared to wild-type, and Prx orthologues are able to inhibit ComR activation by XIP in a reporter strain which lacks an endogenous prx. Additionally, an X-ray crystal structure of Prx reveals a unique fold that implies a novel molecular mechanism to inhibit ComR. Overall, our results suggest Prx functions to inhibit the acquisition of new DNA by Streptococcus. |
format | Online Article Text |
id | pubmed-6224593 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-62245932018-11-13 The conserved mosaic prophage protein paratox inhibits the natural competence regulator ComR in Streptococcus Mashburn-Warren, Lauren Goodman, Steven D. Federle, Michael J. Prehna, Gerd Sci Rep Article Horizontal gene transfer is an important means of bacterial evolution. This includes natural genetic transformation, where bacterial cells become “competent” and DNA is acquired from the extracellular environment. Natural competence in many species of Streptococcus, is regulated by quorum sensing via the ComRS receptor-signal pair. The ComR-XIP (mature ComS peptide) complex induces expression of the alternative sigma factor SigX, which targets RNA polymerase to CIN-box promoters to activate genes involved in DNA uptake and recombination. In addition, the widely distributed Streptococcus prophage gene paratox (prx) also contains a CIN-box, and here we demonstrate it to be transcriptionally activated by XIP. In vitro experiments demonstrate that Prx binds ComR directly and prevents the ComR-XIP complex from interacting with DNA. Mutations of prx in vivo caused increased expression of the late competence gene ssb when induced with XIP as compared to wild-type, and Prx orthologues are able to inhibit ComR activation by XIP in a reporter strain which lacks an endogenous prx. Additionally, an X-ray crystal structure of Prx reveals a unique fold that implies a novel molecular mechanism to inhibit ComR. Overall, our results suggest Prx functions to inhibit the acquisition of new DNA by Streptococcus. Nature Publishing Group UK 2018-11-08 /pmc/articles/PMC6224593/ /pubmed/30409983 http://dx.doi.org/10.1038/s41598-018-34816-7 Text en © The Author(s) 2018 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/. |
spellingShingle | Article Mashburn-Warren, Lauren Goodman, Steven D. Federle, Michael J. Prehna, Gerd The conserved mosaic prophage protein paratox inhibits the natural competence regulator ComR in Streptococcus |
title | The conserved mosaic prophage protein paratox inhibits the natural competence regulator ComR in Streptococcus |
title_full | The conserved mosaic prophage protein paratox inhibits the natural competence regulator ComR in Streptococcus |
title_fullStr | The conserved mosaic prophage protein paratox inhibits the natural competence regulator ComR in Streptococcus |
title_full_unstemmed | The conserved mosaic prophage protein paratox inhibits the natural competence regulator ComR in Streptococcus |
title_short | The conserved mosaic prophage protein paratox inhibits the natural competence regulator ComR in Streptococcus |
title_sort | conserved mosaic prophage protein paratox inhibits the natural competence regulator comr in streptococcus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6224593/ https://www.ncbi.nlm.nih.gov/pubmed/30409983 http://dx.doi.org/10.1038/s41598-018-34816-7 |
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