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J. Bacteriol. doi:10.1128/JB.01520-06
Copyright (c) 2006, American Society for Microbiology and/or the Listed Authors/Institutions. All Rights Reserved.

Dual negative control of spx transcription initiation from the P₃ promoter by repressors PerR and YodB in Bacillus subtilis

Environmental & Biomolecular Systems, OGI School of Science & Engineering, Oregon Health & Science University, Beaverton, Oregon; Graduate School of Information Science, Nara Institute of Science and Technology, 8916-5 Takayama, Ikoma, Nara 630-0192, Japan

	Abstract

The spx gene encodes an RNA polymerase (RNAP)-binding protein that exerts negative and positive transcriptional control in response to oxidative stress in Bacillus subtilis. It resides in the yjbC-spx operon and is transcribed from at least five promoters located in the yjbC regulatory region or in the yjbC-spx intergenic region. Induction of spx transcription in response to treatment with the thiol-specific oxidant, diamide, is the result of transcription initiation at the P₃ promoter located upstream of the spx coding sequence. Previous studies conducted elsewhere, and analyses of transcription factor mutants using transformation array technology have uncovered two transcriptional repressors, PerR and YodB, that target the cis-acting negative control elements of the P₃ promoter. Expression of an spx-bgaB fusion carrying the P₃ promoter is elevated in a yodB or perR mutant, and an additive increase in expression is observed in a yodB perR double mutant. Primer extension analysis of spx RNA shows the same additive increase in P₃ transcript levels in yodB perR mutant cells. Purified YodB and PerR repress spx transcription in vitro when wild type spx P₃ promoter DNA was used as template. Point mutations at positions within the P₃ promoter relieved YodB-dependent repression, while a point mutation at position +24 reduced PerR repression. DNase I footprinting analysis showed that YodB protects a region that includes the P₃ -10 and -35 regions, while PerR binds to a region downstream of the P₃ transcriptional startsite. Binding of both repressors is impaired by treatment of footprinting reactions with diamide or hydrogen peroxide. The study has uncovered a mechanism of dual negative control that relates to the oxidative stress response of Gram-positive bacteria.

This article has been cited by other articles:

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