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QstR-dependent regulation of natural competence and type VI secretion in Vibrio cholerae

During growth on chitinous surfaces in its natural aquatic environment Vibrio cholerae develops natural competence for transformation and kills neighboring non-immune bacteria using a type VI secretion system (T6SS). Activation of these two phenotypes requires the chitin-induced regulator TfoX, but...

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Autores principales: Jaskólska, Milena, Stutzmann, Sandrine, Stoudmann, Candice, Blokesch, Melanie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6237807/
https://www.ncbi.nlm.nih.gov/pubmed/30102403
http://dx.doi.org/10.1093/nar/gky717
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author Jaskólska, Milena
Stutzmann, Sandrine
Stoudmann, Candice
Blokesch, Melanie
author_facet Jaskólska, Milena
Stutzmann, Sandrine
Stoudmann, Candice
Blokesch, Melanie
author_sort Jaskólska, Milena
collection PubMed
description During growth on chitinous surfaces in its natural aquatic environment Vibrio cholerae develops natural competence for transformation and kills neighboring non-immune bacteria using a type VI secretion system (T6SS). Activation of these two phenotypes requires the chitin-induced regulator TfoX, but also integrates signals from quorum sensing via the intermediate regulator QstR, which belongs to the LuxR-type family of regulators. Here, we define the QstR regulon using RNA sequencing. Moreover, by mapping QstR binding sites using chromatin immunoprecipitation coupled with deep sequencing we demonstrate that QstR is a transcription factor that binds upstream of the up- and down-regulated genes. Like other LuxR-type family transcriptional regulators we show that QstR function is dependent on dimerization. However, in contrast to the well-studied LuxR-type biofilm regulator VpsT of V. cholerae, which requires the second messenger c-di-GMP, we show that QstR dimerization and function is c-di-GMP independent. Surprisingly, although ComEA, which is a periplasmic DNA-binding protein essential for transformation, is produced in a QstR-dependent manner, QstR-binding was not detected upstream of comEA suggesting the existence of a further regulatory pathway. Overall, these results provide detailed insights into the function of a key regulator of natural competence and type VI secretion in V. cholerae.
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spelling pubmed-62378072018-11-21 QstR-dependent regulation of natural competence and type VI secretion in Vibrio cholerae Jaskólska, Milena Stutzmann, Sandrine Stoudmann, Candice Blokesch, Melanie Nucleic Acids Res Gene regulation, Chromatin and Epigenetics During growth on chitinous surfaces in its natural aquatic environment Vibrio cholerae develops natural competence for transformation and kills neighboring non-immune bacteria using a type VI secretion system (T6SS). Activation of these two phenotypes requires the chitin-induced regulator TfoX, but also integrates signals from quorum sensing via the intermediate regulator QstR, which belongs to the LuxR-type family of regulators. Here, we define the QstR regulon using RNA sequencing. Moreover, by mapping QstR binding sites using chromatin immunoprecipitation coupled with deep sequencing we demonstrate that QstR is a transcription factor that binds upstream of the up- and down-regulated genes. Like other LuxR-type family transcriptional regulators we show that QstR function is dependent on dimerization. However, in contrast to the well-studied LuxR-type biofilm regulator VpsT of V. cholerae, which requires the second messenger c-di-GMP, we show that QstR dimerization and function is c-di-GMP independent. Surprisingly, although ComEA, which is a periplasmic DNA-binding protein essential for transformation, is produced in a QstR-dependent manner, QstR-binding was not detected upstream of comEA suggesting the existence of a further regulatory pathway. Overall, these results provide detailed insights into the function of a key regulator of natural competence and type VI secretion in V. cholerae. Oxford University Press 2018-11-16 2018-08-08 /pmc/articles/PMC6237807/ /pubmed/30102403 http://dx.doi.org/10.1093/nar/gky717 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Gene regulation, Chromatin and Epigenetics
Jaskólska, Milena
Stutzmann, Sandrine
Stoudmann, Candice
Blokesch, Melanie
QstR-dependent regulation of natural competence and type VI secretion in Vibrio cholerae
title QstR-dependent regulation of natural competence and type VI secretion in Vibrio cholerae
title_full QstR-dependent regulation of natural competence and type VI secretion in Vibrio cholerae
title_fullStr QstR-dependent regulation of natural competence and type VI secretion in Vibrio cholerae
title_full_unstemmed QstR-dependent regulation of natural competence and type VI secretion in Vibrio cholerae
title_short QstR-dependent regulation of natural competence and type VI secretion in Vibrio cholerae
title_sort qstr-dependent regulation of natural competence and type vi secretion in vibrio cholerae
topic Gene regulation, Chromatin and Epigenetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6237807/
https://www.ncbi.nlm.nih.gov/pubmed/30102403
http://dx.doi.org/10.1093/nar/gky717
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