Cargando…

Transcriptional regulation of the operon encoding stress-responsive ECF sigma factor SigH and its anti-sigma factor RshA, and control of its regulatory network in Corynebacterium glutamicum

BACKGROUND: The expression of genes in Corynebacterium glutamicum, a Gram-positive non-pathogenic bacterium used mainly for the industrial production of amino acids, is regulated by seven different sigma factors of RNA polymerase, including the stress-responsive ECF-sigma factor SigH. The sigH gene...

Descripción completa

Detalles Bibliográficos
Autores principales: Busche, Tobias, Šilar, Radoslav, Pičmanová, Martina, Pátek, Miroslav, Kalinowski, Jörn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3489674/
https://www.ncbi.nlm.nih.gov/pubmed/22943411
http://dx.doi.org/10.1186/1471-2164-13-445
_version_ 1782248758635921408
author Busche, Tobias
Šilar, Radoslav
Pičmanová, Martina
Pátek, Miroslav
Kalinowski, Jörn
author_facet Busche, Tobias
Šilar, Radoslav
Pičmanová, Martina
Pátek, Miroslav
Kalinowski, Jörn
author_sort Busche, Tobias
collection PubMed
description BACKGROUND: The expression of genes in Corynebacterium glutamicum, a Gram-positive non-pathogenic bacterium used mainly for the industrial production of amino acids, is regulated by seven different sigma factors of RNA polymerase, including the stress-responsive ECF-sigma factor SigH. The sigH gene is located in a gene cluster together with the rshA gene, putatively encoding an anti-sigma factor. The aim of this study was to analyze the transcriptional regulation of the sigH and rshA gene cluster and the effects of RshA on the SigH regulon, in order to refine the model describing the role of SigH and RshA during stress response. RESULTS: Transcription analyses revealed that the sigH gene and rshA gene are cotranscribed from four sigH housekeeping promoters in C. glutamicum. In addition, a SigH-controlled rshA promoter was found to only drive the transcription of the rshA gene. To test the role of the putative anti-sigma factor gene rshA under normal growth conditions, a C. glutamicum rshA deletion strain was constructed and used for genome-wide transcription profiling with DNA microarrays. In total, 83 genes organized in 61 putative transcriptional units, including those previously detected using sigH mutant strains, exhibited increased transcript levels in the rshA deletion mutant compared to its parental strain. The genes encoding proteins related to disulphide stress response, heat stress proteins, components of the SOS-response to DNA damage and proteasome components were the most markedly upregulated gene groups. Altogether six SigH-dependent promoters upstream of the identified genes were determined by primer extension and a refined consensus promoter consisting of 45 original promoter sequences was constructed. CONCLUSIONS: The rshA gene codes for an anti-sigma factor controlling the function of the stress-responsive sigma factor SigH in C. glutamicum. Transcription of rshA from a SigH-dependent promoter may serve to quickly shutdown the SigH-dependent stress response after the cells have overcome the stress condition. Here we propose a model of the regulation of oxidative and heat stress response including redox homeostasis by SigH, RshA and the thioredoxin system.
format Online
Article
Text
id pubmed-3489674
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-34896742012-11-06 Transcriptional regulation of the operon encoding stress-responsive ECF sigma factor SigH and its anti-sigma factor RshA, and control of its regulatory network in Corynebacterium glutamicum Busche, Tobias Šilar, Radoslav Pičmanová, Martina Pátek, Miroslav Kalinowski, Jörn BMC Genomics Research Article BACKGROUND: The expression of genes in Corynebacterium glutamicum, a Gram-positive non-pathogenic bacterium used mainly for the industrial production of amino acids, is regulated by seven different sigma factors of RNA polymerase, including the stress-responsive ECF-sigma factor SigH. The sigH gene is located in a gene cluster together with the rshA gene, putatively encoding an anti-sigma factor. The aim of this study was to analyze the transcriptional regulation of the sigH and rshA gene cluster and the effects of RshA on the SigH regulon, in order to refine the model describing the role of SigH and RshA during stress response. RESULTS: Transcription analyses revealed that the sigH gene and rshA gene are cotranscribed from four sigH housekeeping promoters in C. glutamicum. In addition, a SigH-controlled rshA promoter was found to only drive the transcription of the rshA gene. To test the role of the putative anti-sigma factor gene rshA under normal growth conditions, a C. glutamicum rshA deletion strain was constructed and used for genome-wide transcription profiling with DNA microarrays. In total, 83 genes organized in 61 putative transcriptional units, including those previously detected using sigH mutant strains, exhibited increased transcript levels in the rshA deletion mutant compared to its parental strain. The genes encoding proteins related to disulphide stress response, heat stress proteins, components of the SOS-response to DNA damage and proteasome components were the most markedly upregulated gene groups. Altogether six SigH-dependent promoters upstream of the identified genes were determined by primer extension and a refined consensus promoter consisting of 45 original promoter sequences was constructed. CONCLUSIONS: The rshA gene codes for an anti-sigma factor controlling the function of the stress-responsive sigma factor SigH in C. glutamicum. Transcription of rshA from a SigH-dependent promoter may serve to quickly shutdown the SigH-dependent stress response after the cells have overcome the stress condition. Here we propose a model of the regulation of oxidative and heat stress response including redox homeostasis by SigH, RshA and the thioredoxin system. BioMed Central 2012-09-03 /pmc/articles/PMC3489674/ /pubmed/22943411 http://dx.doi.org/10.1186/1471-2164-13-445 Text en Copyright ©2012 Busche et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Busche, Tobias
Šilar, Radoslav
Pičmanová, Martina
Pátek, Miroslav
Kalinowski, Jörn
Transcriptional regulation of the operon encoding stress-responsive ECF sigma factor SigH and its anti-sigma factor RshA, and control of its regulatory network in Corynebacterium glutamicum
title Transcriptional regulation of the operon encoding stress-responsive ECF sigma factor SigH and its anti-sigma factor RshA, and control of its regulatory network in Corynebacterium glutamicum
title_full Transcriptional regulation of the operon encoding stress-responsive ECF sigma factor SigH and its anti-sigma factor RshA, and control of its regulatory network in Corynebacterium glutamicum
title_fullStr Transcriptional regulation of the operon encoding stress-responsive ECF sigma factor SigH and its anti-sigma factor RshA, and control of its regulatory network in Corynebacterium glutamicum
title_full_unstemmed Transcriptional regulation of the operon encoding stress-responsive ECF sigma factor SigH and its anti-sigma factor RshA, and control of its regulatory network in Corynebacterium glutamicum
title_short Transcriptional regulation of the operon encoding stress-responsive ECF sigma factor SigH and its anti-sigma factor RshA, and control of its regulatory network in Corynebacterium glutamicum
title_sort transcriptional regulation of the operon encoding stress-responsive ecf sigma factor sigh and its anti-sigma factor rsha, and control of its regulatory network in corynebacterium glutamicum
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3489674/
https://www.ncbi.nlm.nih.gov/pubmed/22943411
http://dx.doi.org/10.1186/1471-2164-13-445
work_keys_str_mv AT buschetobias transcriptionalregulationoftheoperonencodingstressresponsiveecfsigmafactorsighanditsantisigmafactorrshaandcontrolofitsregulatorynetworkincorynebacteriumglutamicum
AT silarradoslav transcriptionalregulationoftheoperonencodingstressresponsiveecfsigmafactorsighanditsantisigmafactorrshaandcontrolofitsregulatorynetworkincorynebacteriumglutamicum
AT picmanovamartina transcriptionalregulationoftheoperonencodingstressresponsiveecfsigmafactorsighanditsantisigmafactorrshaandcontrolofitsregulatorynetworkincorynebacteriumglutamicum
AT patekmiroslav transcriptionalregulationoftheoperonencodingstressresponsiveecfsigmafactorsighanditsantisigmafactorrshaandcontrolofitsregulatorynetworkincorynebacteriumglutamicum
AT kalinowskijorn transcriptionalregulationoftheoperonencodingstressresponsiveecfsigmafactorsighanditsantisigmafactorrshaandcontrolofitsregulatorynetworkincorynebacteriumglutamicum