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A defense-offense multi-layered regulatory switch in a pathogenic bacterium
Cells adapt to environmental changes by efficiently adjusting gene expression programs. Staphylococcus aureus, an opportunistic pathogenic bacterium, switches between defensive and offensive modes in response to quorum sensing signal. We identified and studied the structural characteristics and dyna...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4330369/ https://www.ncbi.nlm.nih.gov/pubmed/25628364 http://dx.doi.org/10.1093/nar/gkv001 |
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author | Nitzan, Mor Fechter, Pierre Peer, Asaf Altuvia, Yael Bronesky, Delphine Vandenesch, François Romby, Pascale Biham, Ofer Margalit, Hanah |
author_facet | Nitzan, Mor Fechter, Pierre Peer, Asaf Altuvia, Yael Bronesky, Delphine Vandenesch, François Romby, Pascale Biham, Ofer Margalit, Hanah |
author_sort | Nitzan, Mor |
collection | PubMed |
description | Cells adapt to environmental changes by efficiently adjusting gene expression programs. Staphylococcus aureus, an opportunistic pathogenic bacterium, switches between defensive and offensive modes in response to quorum sensing signal. We identified and studied the structural characteristics and dynamic properties of the core regulatory circuit governing this switch by deterministic and stochastic computational methods, as well as experimentally. This module, termed here Double Selector Switch (DSS), comprises the RNA regulator RNAIII and the transcription factor Rot, defining a double-layered switch involving both transcriptional and post-transcriptional regulations. It coordinates the inverse expression of two sets of target genes, immuno-modulators and exotoxins, expressed during the defensive and offensive modes, respectively. Our computational and experimental analyses show that the DSS guarantees fine-tuned coordination of the inverse expression of its two gene sets, tight regulation, and filtering of noisy signals. We also identified variants of this circuit in other bacterial systems, suggesting it is used as a molecular switch in various cellular contexts and offering its use as a template for an effective switching device in synthetic biology studies. |
format | Online Article Text |
id | pubmed-4330369 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-43303692015-03-18 A defense-offense multi-layered regulatory switch in a pathogenic bacterium Nitzan, Mor Fechter, Pierre Peer, Asaf Altuvia, Yael Bronesky, Delphine Vandenesch, François Romby, Pascale Biham, Ofer Margalit, Hanah Nucleic Acids Res Computational Biology Cells adapt to environmental changes by efficiently adjusting gene expression programs. Staphylococcus aureus, an opportunistic pathogenic bacterium, switches between defensive and offensive modes in response to quorum sensing signal. We identified and studied the structural characteristics and dynamic properties of the core regulatory circuit governing this switch by deterministic and stochastic computational methods, as well as experimentally. This module, termed here Double Selector Switch (DSS), comprises the RNA regulator RNAIII and the transcription factor Rot, defining a double-layered switch involving both transcriptional and post-transcriptional regulations. It coordinates the inverse expression of two sets of target genes, immuno-modulators and exotoxins, expressed during the defensive and offensive modes, respectively. Our computational and experimental analyses show that the DSS guarantees fine-tuned coordination of the inverse expression of its two gene sets, tight regulation, and filtering of noisy signals. We also identified variants of this circuit in other bacterial systems, suggesting it is used as a molecular switch in various cellular contexts and offering its use as a template for an effective switching device in synthetic biology studies. Oxford University Press 2015-02-18 2015-01-27 /pmc/articles/PMC4330369/ /pubmed/25628364 http://dx.doi.org/10.1093/nar/gkv001 Text en © The Author(s) 2015. 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 | Computational Biology Nitzan, Mor Fechter, Pierre Peer, Asaf Altuvia, Yael Bronesky, Delphine Vandenesch, François Romby, Pascale Biham, Ofer Margalit, Hanah A defense-offense multi-layered regulatory switch in a pathogenic bacterium |
title | A defense-offense multi-layered regulatory switch in a pathogenic bacterium |
title_full | A defense-offense multi-layered regulatory switch in a pathogenic bacterium |
title_fullStr | A defense-offense multi-layered regulatory switch in a pathogenic bacterium |
title_full_unstemmed | A defense-offense multi-layered regulatory switch in a pathogenic bacterium |
title_short | A defense-offense multi-layered regulatory switch in a pathogenic bacterium |
title_sort | defense-offense multi-layered regulatory switch in a pathogenic bacterium |
topic | Computational Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4330369/ https://www.ncbi.nlm.nih.gov/pubmed/25628364 http://dx.doi.org/10.1093/nar/gkv001 |
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