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A positive feedback loop mediated by Sigma X enhances expression of the streptococcal regulator ComR
Natural transformation is used by bacteria to take up DNA from their surroundings and incorporate it into their genomes. Streptococci do so during a transient period of competence, triggered by pheromones that they produce, secrete and sense under conditions influenced by the environment. In Strepto...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5519730/ https://www.ncbi.nlm.nih.gov/pubmed/28729683 http://dx.doi.org/10.1038/s41598-017-04768-5 |
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author | Khan, Rabia Junges, Roger Åmdal, Heidi A. Chen, Tsute Morrison, Donald A. Petersen, Fernanda C. |
author_facet | Khan, Rabia Junges, Roger Åmdal, Heidi A. Chen, Tsute Morrison, Donald A. Petersen, Fernanda C. |
author_sort | Khan, Rabia |
collection | PubMed |
description | Natural transformation is used by bacteria to take up DNA from their surroundings and incorporate it into their genomes. Streptococci do so during a transient period of competence, triggered by pheromones that they produce, secrete and sense under conditions influenced by the environment. In Streptococcus mutans, Streptococcus suis, and species of the bovis, salivarius and pyogenic groups of streptococci, the pheromone XIP is sensed by the intra-cellular regulator ComR, that in turn activates the transcription of comS, encoding the XIP precursor, and of sigX, encoding the only known alternative sigma factor in streptococci. Although induction of comR during competence has been known for more than fifteen years, the mechanism regulating its expression remains unidentified. By a combination of directional RNA-sequencing, optimal competence conditions, stepwise deletions and marker-less genome editing, we found that SigX is the missing link in overproduction of ComR. In the absence of comR induction, both sigX expression and transformation were significantly reduced. Placing comR and comS transcripts under the control of different regulators so as to form two interlocked positive feedback circuits may enable S. mutans to fine-tune the kinetics and magnitude of the competence response according to their need. |
format | Online Article Text |
id | pubmed-5519730 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55197302017-07-26 A positive feedback loop mediated by Sigma X enhances expression of the streptococcal regulator ComR Khan, Rabia Junges, Roger Åmdal, Heidi A. Chen, Tsute Morrison, Donald A. Petersen, Fernanda C. Sci Rep Article Natural transformation is used by bacteria to take up DNA from their surroundings and incorporate it into their genomes. Streptococci do so during a transient period of competence, triggered by pheromones that they produce, secrete and sense under conditions influenced by the environment. In Streptococcus mutans, Streptococcus suis, and species of the bovis, salivarius and pyogenic groups of streptococci, the pheromone XIP is sensed by the intra-cellular regulator ComR, that in turn activates the transcription of comS, encoding the XIP precursor, and of sigX, encoding the only known alternative sigma factor in streptococci. Although induction of comR during competence has been known for more than fifteen years, the mechanism regulating its expression remains unidentified. By a combination of directional RNA-sequencing, optimal competence conditions, stepwise deletions and marker-less genome editing, we found that SigX is the missing link in overproduction of ComR. In the absence of comR induction, both sigX expression and transformation were significantly reduced. Placing comR and comS transcripts under the control of different regulators so as to form two interlocked positive feedback circuits may enable S. mutans to fine-tune the kinetics and magnitude of the competence response according to their need. Nature Publishing Group UK 2017-07-20 /pmc/articles/PMC5519730/ /pubmed/28729683 http://dx.doi.org/10.1038/s41598-017-04768-5 Text en © The Author(s) 2017 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 Khan, Rabia Junges, Roger Åmdal, Heidi A. Chen, Tsute Morrison, Donald A. Petersen, Fernanda C. A positive feedback loop mediated by Sigma X enhances expression of the streptococcal regulator ComR |
title | A positive feedback loop mediated by Sigma X enhances expression of the streptococcal regulator ComR |
title_full | A positive feedback loop mediated by Sigma X enhances expression of the streptococcal regulator ComR |
title_fullStr | A positive feedback loop mediated by Sigma X enhances expression of the streptococcal regulator ComR |
title_full_unstemmed | A positive feedback loop mediated by Sigma X enhances expression of the streptococcal regulator ComR |
title_short | A positive feedback loop mediated by Sigma X enhances expression of the streptococcal regulator ComR |
title_sort | positive feedback loop mediated by sigma x enhances expression of the streptococcal regulator comr |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5519730/ https://www.ncbi.nlm.nih.gov/pubmed/28729683 http://dx.doi.org/10.1038/s41598-017-04768-5 |
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