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PMID: 18230178 Published · epublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Genome-wide transcriptome analysis reveals that a pleiotropic antibiotic regulator, AfsS, modulates nutritional stress response in Streptomyces coelicolor A3(2).

BMC genomics ·Vol. 9 ·2008-01-29 ·Pages 56

Lian W, Jayapal KP, Charaniya S, Mehra S, Glod F, Kyung YS, Sherman DH, Hu WS

Abstract

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. 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. 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.

MeSH Terms
Anthraquinones/metabolism Anti-Bacterial Agents/biosynthesis,metabolism Bacterial Proteins/genetics,metabolism Chromosomes, Bacterial Gene Expression Profiling Gene Expression Regulation, Bacterial Genes, Bacterial Genome, Bacterial/genetics Glutamate-Ammonia Ligase/genetics,metabolism Kinetics Mutation Nitrogen/metabolism Oligonucleotide Array Sequence Analysis Phosphates/deficiency Principal Component Analysis Reproducibility of Results Reverse Transcriptase Polymerase Chain Reaction Sigma Factor/chemistry,metabolism Signal Transduction/genetics Streptomyces coelicolor/enzymology,genetics,metabolism Sulfates/metabolism Thiosulfate Sulfurtransferase/genetics,metabolism Transcription, Genetic/genetics
Chemicals
Anthraquinones Anti-Bacterial Agents Bacterial Proteins Phosphates Sigma Factor Sulfates Thiosulfate Sulfurtransferase Glutamate-Ammonia Ligase actinorhodin Nitrogen
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Lian Wei
Department of Chemical Engineering and Materials Science, University of Minnesota, 421 Washington Ave. SE., Minneapolis, MN 55455, USA. wei.lian@abbott.com
Jayapal Karthik P
Charaniya Salim
Mehra Sarika
Glod Frank
Kyung Yun-Seung
Sherman David H
Hu Wei-Shou
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Article Info
Journal
BMC genomics
Abbr.
BMC Genomics
ISSN
1471-2164
Published
2008-01-29
Epub
2008-00-29
Pages
56
Language
English
Region
England
NLM ID
100965258
PMCID
PMC2267785
Subset
IM
Grants
NIGMS NIH HHS · R01 GM055850 · United States
NIGMS NIH HHS · GM55850 · United States
Databases
Analysis Services
Analysis Services

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