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Genome-Wide Analysis of In Vivo Binding of the Master Regulator DasR in Streptomyces coelicolor Identifies Novel Non-Canonical Targets

Streptomycetes produce a wealth of natural products, including over half of all known antibiotics. It was previously demonstrated that N-acetylglucosamine and secondary metabolism are closely entwined in streptomycetes. Here we show that DNA recognition by the N-acetylglucosamine-responsive regulato...

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Autores principales: Świątek-Połatyńska, Magdalena A., Bucca, Giselda, Laing, Emma, Gubbens, Jacob, Titgemeyer, Fritz, Smith, Colin P., Rigali, Sébastien, van Wezel, Gilles P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4398421/
https://www.ncbi.nlm.nih.gov/pubmed/25875084
http://dx.doi.org/10.1371/journal.pone.0122479
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author Świątek-Połatyńska, Magdalena A.
Bucca, Giselda
Laing, Emma
Gubbens, Jacob
Titgemeyer, Fritz
Smith, Colin P.
Rigali, Sébastien
van Wezel, Gilles P.
author_facet Świątek-Połatyńska, Magdalena A.
Bucca, Giselda
Laing, Emma
Gubbens, Jacob
Titgemeyer, Fritz
Smith, Colin P.
Rigali, Sébastien
van Wezel, Gilles P.
author_sort Świątek-Połatyńska, Magdalena A.
collection PubMed
description Streptomycetes produce a wealth of natural products, including over half of all known antibiotics. It was previously demonstrated that N-acetylglucosamine and secondary metabolism are closely entwined in streptomycetes. Here we show that DNA recognition by the N-acetylglucosamine-responsive regulator DasR is growth-phase dependent, and that DasR can bind to sites in the S. coelicolor genome that have no obvious resemblance to previously identified DasR-responsive elements. Thus, the regulon of DasR extends well beyond what was previously predicted and includes a large number of genes with functions far removed from N-acetylglucosamine metabolism, such as genes for small RNAs and DNA transposases. Conversely, the DasR regulon during vegetative growth largely correlates to the presence of canonical DasR-responsive elements. The changes in DasR binding in vivo following N-acetylglucosamine induction were studied in detail and a possible molecular mechanism by which the influence of DasR is extended is discussed. Discussion of DasR binding was further informed by a parallel transcriptome analysis of the respective cultures. Evidence is provided that DasR binds directly to the promoters of all genes encoding pathway-specific regulators of antibiotic production in S. coelicolor, thereby providing an exquisitely simple link between nutritional control and secondary metabolism.
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spelling pubmed-43984212015-04-21 Genome-Wide Analysis of In Vivo Binding of the Master Regulator DasR in Streptomyces coelicolor Identifies Novel Non-Canonical Targets Świątek-Połatyńska, Magdalena A. Bucca, Giselda Laing, Emma Gubbens, Jacob Titgemeyer, Fritz Smith, Colin P. Rigali, Sébastien van Wezel, Gilles P. PLoS One Research Article Streptomycetes produce a wealth of natural products, including over half of all known antibiotics. It was previously demonstrated that N-acetylglucosamine and secondary metabolism are closely entwined in streptomycetes. Here we show that DNA recognition by the N-acetylglucosamine-responsive regulator DasR is growth-phase dependent, and that DasR can bind to sites in the S. coelicolor genome that have no obvious resemblance to previously identified DasR-responsive elements. Thus, the regulon of DasR extends well beyond what was previously predicted and includes a large number of genes with functions far removed from N-acetylglucosamine metabolism, such as genes for small RNAs and DNA transposases. Conversely, the DasR regulon during vegetative growth largely correlates to the presence of canonical DasR-responsive elements. The changes in DasR binding in vivo following N-acetylglucosamine induction were studied in detail and a possible molecular mechanism by which the influence of DasR is extended is discussed. Discussion of DasR binding was further informed by a parallel transcriptome analysis of the respective cultures. Evidence is provided that DasR binds directly to the promoters of all genes encoding pathway-specific regulators of antibiotic production in S. coelicolor, thereby providing an exquisitely simple link between nutritional control and secondary metabolism. Public Library of Science 2015-04-15 /pmc/articles/PMC4398421/ /pubmed/25875084 http://dx.doi.org/10.1371/journal.pone.0122479 Text en © 2015 Świątek-Połatyńska et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Świątek-Połatyńska, Magdalena A.
Bucca, Giselda
Laing, Emma
Gubbens, Jacob
Titgemeyer, Fritz
Smith, Colin P.
Rigali, Sébastien
van Wezel, Gilles P.
Genome-Wide Analysis of In Vivo Binding of the Master Regulator DasR in Streptomyces coelicolor Identifies Novel Non-Canonical Targets
title Genome-Wide Analysis of In Vivo Binding of the Master Regulator DasR in Streptomyces coelicolor Identifies Novel Non-Canonical Targets
title_full Genome-Wide Analysis of In Vivo Binding of the Master Regulator DasR in Streptomyces coelicolor Identifies Novel Non-Canonical Targets
title_fullStr Genome-Wide Analysis of In Vivo Binding of the Master Regulator DasR in Streptomyces coelicolor Identifies Novel Non-Canonical Targets
title_full_unstemmed Genome-Wide Analysis of In Vivo Binding of the Master Regulator DasR in Streptomyces coelicolor Identifies Novel Non-Canonical Targets
title_short Genome-Wide Analysis of In Vivo Binding of the Master Regulator DasR in Streptomyces coelicolor Identifies Novel Non-Canonical Targets
title_sort genome-wide analysis of in vivo binding of the master regulator dasr in streptomyces coelicolor identifies novel non-canonical targets
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4398421/
https://www.ncbi.nlm.nih.gov/pubmed/25875084
http://dx.doi.org/10.1371/journal.pone.0122479
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