Cargando…
Evolutionary expansion of a regulatory network by counter-silencing
Horizontal gene transfer plays a major role in bacterial evolution. Successful acquisition of new genes requires their incorporation into existing regulatory networks. This study compares the regulation of conserved genes in the PhoPQ regulon of Salmonella enterica serovar Typhimurium with that of P...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4215172/ https://www.ncbi.nlm.nih.gov/pubmed/25348042 http://dx.doi.org/10.1038/ncomms6270 |
_version_ | 1782342054661062656 |
---|---|
author | Will, William R. Bale, Denise H. Reid, Philip J. Libby, Stephen J. Fang, Ferric C. |
author_facet | Will, William R. Bale, Denise H. Reid, Philip J. Libby, Stephen J. Fang, Ferric C. |
author_sort | Will, William R. |
collection | PubMed |
description | Horizontal gene transfer plays a major role in bacterial evolution. Successful acquisition of new genes requires their incorporation into existing regulatory networks. This study compares the regulation of conserved genes in the PhoPQ regulon of Salmonella enterica serovar Typhimurium with that of PhoPQ-regulated horizontally-acquired genes, which are silenced by the histone-like protein H-NS. We demonstrate that PhoP up-regulates conserved and horizontally-acquired genes by distinct mechanisms. Conserved genes are regulated by classical PhoP-mediated activation and are invariant in promoter architecture, whereas horizontally-acquired genes exhibit variable promoter architecture and are regulated by PhoP-mediated counter-silencing. Biochemical analyses show that a horizontally-acquired promoter adopts different structures in the silenced and counter-silenced states, implicating the remodeling of the H-NS nucleoprotein filament and the subsequent restoration of open complex formation as the central mechanism of counter-silencing. Our results indicate that counter-silencing is favored in the regulatory integration of newly-acquired genes because it is able to accommodate multiple promoter architectures. |
format | Online Article Text |
id | pubmed-4215172 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
record_format | MEDLINE/PubMed |
spelling | pubmed-42151722015-04-28 Evolutionary expansion of a regulatory network by counter-silencing Will, William R. Bale, Denise H. Reid, Philip J. Libby, Stephen J. Fang, Ferric C. Nat Commun Article Horizontal gene transfer plays a major role in bacterial evolution. Successful acquisition of new genes requires their incorporation into existing regulatory networks. This study compares the regulation of conserved genes in the PhoPQ regulon of Salmonella enterica serovar Typhimurium with that of PhoPQ-regulated horizontally-acquired genes, which are silenced by the histone-like protein H-NS. We demonstrate that PhoP up-regulates conserved and horizontally-acquired genes by distinct mechanisms. Conserved genes are regulated by classical PhoP-mediated activation and are invariant in promoter architecture, whereas horizontally-acquired genes exhibit variable promoter architecture and are regulated by PhoP-mediated counter-silencing. Biochemical analyses show that a horizontally-acquired promoter adopts different structures in the silenced and counter-silenced states, implicating the remodeling of the H-NS nucleoprotein filament and the subsequent restoration of open complex formation as the central mechanism of counter-silencing. Our results indicate that counter-silencing is favored in the regulatory integration of newly-acquired genes because it is able to accommodate multiple promoter architectures. 2014-10-28 /pmc/articles/PMC4215172/ /pubmed/25348042 http://dx.doi.org/10.1038/ncomms6270 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Will, William R. Bale, Denise H. Reid, Philip J. Libby, Stephen J. Fang, Ferric C. Evolutionary expansion of a regulatory network by counter-silencing |
title | Evolutionary expansion of a regulatory network by counter-silencing |
title_full | Evolutionary expansion of a regulatory network by counter-silencing |
title_fullStr | Evolutionary expansion of a regulatory network by counter-silencing |
title_full_unstemmed | Evolutionary expansion of a regulatory network by counter-silencing |
title_short | Evolutionary expansion of a regulatory network by counter-silencing |
title_sort | evolutionary expansion of a regulatory network by counter-silencing |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4215172/ https://www.ncbi.nlm.nih.gov/pubmed/25348042 http://dx.doi.org/10.1038/ncomms6270 |
work_keys_str_mv | AT willwilliamr evolutionaryexpansionofaregulatorynetworkbycountersilencing AT baledeniseh evolutionaryexpansionofaregulatorynetworkbycountersilencing AT reidphilipj evolutionaryexpansionofaregulatorynetworkbycountersilencing AT libbystephenj evolutionaryexpansionofaregulatorynetworkbycountersilencing AT fangferricc evolutionaryexpansionofaregulatorynetworkbycountersilencing |