Cargando…
Genome-wide transcriptome analysis reveals that a pleiotropic antibiotic regulator, AfsS, modulates nutritional stress response in Streptomyces coelicolor A3(2)
BACKGROUND: A small "sigma-like" protein, AfsS, pleiotropically regulates antibiotic biosynthesis in Streptomyces coelicolor. Overexpression of afsS in S. coelicolor and certain related species causes antibiotic stimulatory effects in the host organism. Although recent studies have uncover...
Autores principales: | , , , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2008
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2267785/ https://www.ncbi.nlm.nih.gov/pubmed/18230178 http://dx.doi.org/10.1186/1471-2164-9-56 |
_version_ | 1782151657668214784 |
---|---|
author | Lian, Wei Jayapal, Karthik P Charaniya, Salim Mehra, Sarika Glod, Frank Kyung, Yun-Seung Sherman, David H Hu, Wei-Shou |
author_facet | Lian, Wei Jayapal, Karthik P Charaniya, Salim Mehra, Sarika Glod, Frank Kyung, Yun-Seung Sherman, David H Hu, Wei-Shou |
author_sort | Lian, Wei |
collection | PubMed |
description | BACKGROUND: A small "sigma-like" protein, AfsS, pleiotropically regulates antibiotic biosynthesis in Streptomyces coelicolor. Overexpression of afsS in S. coelicolor and certain related species causes antibiotic stimulatory effects in the host organism. Although recent studies have uncovered some of the upstream events activating this gene, the mechanisms through which this signal is relayed downstream leading to the eventual induction of antibiotic pathways remain unclear. RESULTS: In this study, we employed whole-genome DNA microarrays and quantitative PCRs to examine the transcriptome of an afsS disruption mutant that is completely deficient in the production of actinorhodin, a major S. coelicolor antibiotic. The production of undecylprodigiosin, another prominent antibiotic, was, however, perturbed only marginally in the mutant. Principal component analysis of temporal gene expression profiles identified two major gene classes each exhibiting a distinct coordinate differential expression pattern. Surprisingly, nearly 70% of the >117 differentially expressed genes were conspicuously associated with nutrient starvation response, particularly those of phosphate, nitrogen and sulfate. Furthermore, expression profiles of some transcriptional regulators including at least two sigma factors were perturbed in the mutant. In almost every case, the effect of afsS disruption was not observed until the onset of stationary phase. CONCLUSION: Our data suggests a comprehensive role for S. coelicolor AfsS as a master regulator of both antibiotic synthesis and nutritional stress response, reminiscent of alternative sigma factors found in several bacteria. |
format | Text |
id | pubmed-2267785 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-22677852008-03-15 Genome-wide transcriptome analysis reveals that a pleiotropic antibiotic regulator, AfsS, modulates nutritional stress response in Streptomyces coelicolor A3(2) Lian, Wei Jayapal, Karthik P Charaniya, Salim Mehra, Sarika Glod, Frank Kyung, Yun-Seung Sherman, David H Hu, Wei-Shou BMC Genomics Research Article BACKGROUND: A small "sigma-like" protein, AfsS, pleiotropically regulates antibiotic biosynthesis in Streptomyces coelicolor. Overexpression of afsS in S. coelicolor and certain related species causes antibiotic stimulatory effects in the host organism. Although recent studies have uncovered some of the upstream events activating this gene, the mechanisms through which this signal is relayed downstream leading to the eventual induction of antibiotic pathways remain unclear. RESULTS: In this study, we employed whole-genome DNA microarrays and quantitative PCRs to examine the transcriptome of an afsS disruption mutant that is completely deficient in the production of actinorhodin, a major S. coelicolor antibiotic. The production of undecylprodigiosin, another prominent antibiotic, was, however, perturbed only marginally in the mutant. Principal component analysis of temporal gene expression profiles identified two major gene classes each exhibiting a distinct coordinate differential expression pattern. Surprisingly, nearly 70% of the >117 differentially expressed genes were conspicuously associated with nutrient starvation response, particularly those of phosphate, nitrogen and sulfate. Furthermore, expression profiles of some transcriptional regulators including at least two sigma factors were perturbed in the mutant. In almost every case, the effect of afsS disruption was not observed until the onset of stationary phase. CONCLUSION: Our data suggests a comprehensive role for S. coelicolor AfsS as a master regulator of both antibiotic synthesis and nutritional stress response, reminiscent of alternative sigma factors found in several bacteria. BioMed Central 2008-01-29 /pmc/articles/PMC2267785/ /pubmed/18230178 http://dx.doi.org/10.1186/1471-2164-9-56 Text en Copyright © 2008 Lian 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 Lian, Wei Jayapal, Karthik P Charaniya, Salim Mehra, Sarika Glod, Frank Kyung, Yun-Seung Sherman, David H Hu, Wei-Shou Genome-wide transcriptome analysis reveals that a pleiotropic antibiotic regulator, AfsS, modulates nutritional stress response in Streptomyces coelicolor A3(2) |
title | Genome-wide transcriptome analysis reveals that a pleiotropic antibiotic regulator, AfsS, modulates nutritional stress response in Streptomyces coelicolor A3(2) |
title_full | Genome-wide transcriptome analysis reveals that a pleiotropic antibiotic regulator, AfsS, modulates nutritional stress response in Streptomyces coelicolor A3(2) |
title_fullStr | Genome-wide transcriptome analysis reveals that a pleiotropic antibiotic regulator, AfsS, modulates nutritional stress response in Streptomyces coelicolor A3(2) |
title_full_unstemmed | Genome-wide transcriptome analysis reveals that a pleiotropic antibiotic regulator, AfsS, modulates nutritional stress response in Streptomyces coelicolor A3(2) |
title_short | Genome-wide transcriptome analysis reveals that a pleiotropic antibiotic regulator, AfsS, modulates nutritional stress response in Streptomyces coelicolor A3(2) |
title_sort | genome-wide transcriptome analysis reveals that a pleiotropic antibiotic regulator, afss, modulates nutritional stress response in streptomyces coelicolor a3(2) |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2267785/ https://www.ncbi.nlm.nih.gov/pubmed/18230178 http://dx.doi.org/10.1186/1471-2164-9-56 |
work_keys_str_mv | AT lianwei genomewidetranscriptomeanalysisrevealsthatapleiotropicantibioticregulatorafssmodulatesnutritionalstressresponseinstreptomycescoelicolora32 AT jayapalkarthikp genomewidetranscriptomeanalysisrevealsthatapleiotropicantibioticregulatorafssmodulatesnutritionalstressresponseinstreptomycescoelicolora32 AT charaniyasalim genomewidetranscriptomeanalysisrevealsthatapleiotropicantibioticregulatorafssmodulatesnutritionalstressresponseinstreptomycescoelicolora32 AT mehrasarika genomewidetranscriptomeanalysisrevealsthatapleiotropicantibioticregulatorafssmodulatesnutritionalstressresponseinstreptomycescoelicolora32 AT glodfrank genomewidetranscriptomeanalysisrevealsthatapleiotropicantibioticregulatorafssmodulatesnutritionalstressresponseinstreptomycescoelicolora32 AT kyungyunseung genomewidetranscriptomeanalysisrevealsthatapleiotropicantibioticregulatorafssmodulatesnutritionalstressresponseinstreptomycescoelicolora32 AT shermandavidh genomewidetranscriptomeanalysisrevealsthatapleiotropicantibioticregulatorafssmodulatesnutritionalstressresponseinstreptomycescoelicolora32 AT huweishou genomewidetranscriptomeanalysisrevealsthatapleiotropicantibioticregulatorafssmodulatesnutritionalstressresponseinstreptomycescoelicolora32 |