RRC ID 53799
Author Kosono S, Asai K, Sadaie Y, Kudo T.
Title Altered gene expression in the transition phase by disruption of a Na+/H+ antiporter gene (shaA) in Bacillus subtilis.
Journal FEMS Microbiol Lett
Abstract The shaA gene (sodium-hydrogen antiporter gene A, identical to mrpA) is largely responsible for Na+ extrusion in Bacillus subtilis. The disruption of shaA combined with a low concentration of NaCl completely abolishes sporulation but allows normal growth. To investigate the role of shaA and shaA-mediated sodium ion homeostasis in sporulation, we performed a comprehensive study of expression profiles of eight alternative sigma factors, sigmaB and the seven extracytoplasmic function sigma factors (sigmaM, sigmaV, sigmaW, sigmaX, sigmaY, sigmaZ, and sigmaYlaC) in an attempt to determine the global change of gene expression that results from a disturbance of Na+ homeostasis caused by shaA disruption. Induction of sigmaB activity in the transition phase was impaired in the shaA mutant, and this effect was enhanced in the presence of 30 mM NaCl. Salt stress activation of sigmaB occurred normally in the shaA mutant. sigmaM-, sigmaW-, sigmaX-dependent transcription and sigZ transcription was also induced in the transition phase of the wild-type, which was modulated by shaA disruption. The induction of sigmaM-dependent transcription was enhanced in the shaA mutant, while that of sigmaX-dependent transcription and sigZ transcription was decreased. sigmaW-dependent transcription was increased throughout the growth phase of the shaA mutant, which was consistent with the result of proteome analysis. We conclude that shaA disruption resulted in the modulated induction of alternative sigma factor activities, which would be problematic for the cell upon entering the sporulation stage.
Volume 232(1)
Pages 93-9
Published 2004-3-12
DOI 10.1016/S0378-1097(04)00037-0
PII S0378109704000370
PMID 15019740
MeSH Artificial Gene Fusion Bacillus subtilis / genetics* Bacillus subtilis / growth & development Bacillus subtilis / metabolism* Bacterial Proteins / analysis Bacterial Proteins / biosynthesis* Bacterial Proteins / genetics Gene Expression Regulation, Bacterial* / physiology Genes, Bacterial Genes, Reporter Lac Operon / genetics Proteome / analysis Sigma Factor / biosynthesis* Sigma Factor / genetics Sodium Chloride / metabolism Sodium-Hydrogen Exchangers / genetics* Sodium-Hydrogen Exchangers / physiology* Spores, Bacterial / genetics Spores, Bacterial / growth & development beta-Galactosidase / genetics beta-Galactosidase / metabolism
IF 1.994
Times Cited 17
Resource
Prokaryotes B. subtilis MBS615 MBS616 MBS617