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...

Descripción completa

Detalles Bibliográficos
Autores principales: Will, William R., Bale, Denise H., Reid, Philip J., Libby, Stephen J., Fang, Ferric C.
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