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Canonical and non-canonical EcfG sigma factors control the general stress response in Rhizobium etli
A core component of the α-proteobacterial general stress response (GSR) is the extracytoplasmic function (ECF) sigma factor EcfG, exclusively present in this taxonomic class. Half of the completed α-proteobacterial genome sequences contain two or more copies of genes encoding σ(EcfG)-like sigma fact...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3892343/ https://www.ncbi.nlm.nih.gov/pubmed/24311555 http://dx.doi.org/10.1002/mbo3.137 |
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author | Jans, Ann Vercruysse, Maarten Gao, Shanjun Engelen, Kristof Lambrichts, Ivo Fauvart, Maarten Michiels, Jan |
author_facet | Jans, Ann Vercruysse, Maarten Gao, Shanjun Engelen, Kristof Lambrichts, Ivo Fauvart, Maarten Michiels, Jan |
author_sort | Jans, Ann |
collection | PubMed |
description | A core component of the α-proteobacterial general stress response (GSR) is the extracytoplasmic function (ECF) sigma factor EcfG, exclusively present in this taxonomic class. Half of the completed α-proteobacterial genome sequences contain two or more copies of genes encoding σ(EcfG)-like sigma factors, with the primary copy typically located adjacent to genes coding for a cognate anti-sigma factor (NepR) and two-component response regulator (PhyR). So far, the widespread occurrence of additional, non-canonical σ(EcfG) copies has not satisfactorily been explained. This study explores the hierarchical relation between Rhizobium etli σ(EcfG1) and σ(EcfG2), canonical and non-canonical σ(EcfG) proteins, respectively. Contrary to reports in other species, we find that σ(EcfG1) and σ(EcfG2) act in parallel, as nodes of a complex regulatory network, rather than in series, as elements of a linear regulatory cascade. We demonstrate that both sigma factors control unique yet also shared target genes, corroborating phenotypic evidence. σ(EcfG1) drives expression of rpoH2, explaining the increased heat sensitivity of an ecfG1 mutant, while katG is under control of σ(EcfG2), accounting for reduced oxidative stress resistance of an ecfG2 mutant. We also identify non-coding RNA genes as novel σ(EcfG) targets. We propose a modified model for GSR regulation in R. etli, in which σ(EcfG1) and σ(EcfG2) function largely independently. Based on a phylogenetic analysis and considering the prevalence of α-proteobacterial genomes with multiple σ(EcfG) copies, this model may also be applicable to numerous other species. |
format | Online Article Text |
id | pubmed-3892343 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-38923432014-01-21 Canonical and non-canonical EcfG sigma factors control the general stress response in Rhizobium etli Jans, Ann Vercruysse, Maarten Gao, Shanjun Engelen, Kristof Lambrichts, Ivo Fauvart, Maarten Michiels, Jan Microbiologyopen Original Research A core component of the α-proteobacterial general stress response (GSR) is the extracytoplasmic function (ECF) sigma factor EcfG, exclusively present in this taxonomic class. Half of the completed α-proteobacterial genome sequences contain two or more copies of genes encoding σ(EcfG)-like sigma factors, with the primary copy typically located adjacent to genes coding for a cognate anti-sigma factor (NepR) and two-component response regulator (PhyR). So far, the widespread occurrence of additional, non-canonical σ(EcfG) copies has not satisfactorily been explained. This study explores the hierarchical relation between Rhizobium etli σ(EcfG1) and σ(EcfG2), canonical and non-canonical σ(EcfG) proteins, respectively. Contrary to reports in other species, we find that σ(EcfG1) and σ(EcfG2) act in parallel, as nodes of a complex regulatory network, rather than in series, as elements of a linear regulatory cascade. We demonstrate that both sigma factors control unique yet also shared target genes, corroborating phenotypic evidence. σ(EcfG1) drives expression of rpoH2, explaining the increased heat sensitivity of an ecfG1 mutant, while katG is under control of σ(EcfG2), accounting for reduced oxidative stress resistance of an ecfG2 mutant. We also identify non-coding RNA genes as novel σ(EcfG) targets. We propose a modified model for GSR regulation in R. etli, in which σ(EcfG1) and σ(EcfG2) function largely independently. Based on a phylogenetic analysis and considering the prevalence of α-proteobacterial genomes with multiple σ(EcfG) copies, this model may also be applicable to numerous other species. Blackwell Publishing Ltd 2013-12 2013-10-28 /pmc/articles/PMC3892343/ /pubmed/24311555 http://dx.doi.org/10.1002/mbo3.137 Text en © 2013 Published by John Wiley & Sons Ltd http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation. |
spellingShingle | Original Research Jans, Ann Vercruysse, Maarten Gao, Shanjun Engelen, Kristof Lambrichts, Ivo Fauvart, Maarten Michiels, Jan Canonical and non-canonical EcfG sigma factors control the general stress response in Rhizobium etli |
title | Canonical and non-canonical EcfG sigma factors control the general stress response in Rhizobium etli |
title_full | Canonical and non-canonical EcfG sigma factors control the general stress response in Rhizobium etli |
title_fullStr | Canonical and non-canonical EcfG sigma factors control the general stress response in Rhizobium etli |
title_full_unstemmed | Canonical and non-canonical EcfG sigma factors control the general stress response in Rhizobium etli |
title_short | Canonical and non-canonical EcfG sigma factors control the general stress response in Rhizobium etli |
title_sort | canonical and non-canonical ecfg sigma factors control the general stress response in rhizobium etli |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3892343/ https://www.ncbi.nlm.nih.gov/pubmed/24311555 http://dx.doi.org/10.1002/mbo3.137 |
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