Affiliation:
1. Institute of Oceanic Research and Development, Tokai University, Shizuoka, Japan
2. Department of Bioscience, Tokyo University of Agriculture, Tokyo, Japan
Abstract
ABSTRACT
Bacillus subtilis
DegU is a response regulator of the DegS-DegU two-component regulatory system. Phosphorylated DegU (DegU-P) controls many genes and biological processes, such as exoprotease and γ-polyglutamic acid production, in addition to the
degU
gene, by binding to target gene promoters. Nonphosphorylated DegU and low levels of DegU-P are required for swarming motility and genetic competence. The DNA-binding repressors SinR and SlrR are part of a double-negative feedback loop and comprise the epigenetic switch governing biofilm formation. In this study, we found that SinR repressed
degU
. Furthermore, SlrR, which interacts with SinR through protein-protein interaction, seems to have an active role in
degU
expression in
in vivo lacZ
analysis. An
in vitro
transcription assay supported this observation. An electrophoretic mobility shift assay (EMSA) showed that SinR bound to the
degU
promoter and that SlrR formed a complex with SinR on the
degU
promoter. In EMSA, DegU-P excluded the SinR/SlrR complex but not SinR from the
degU
promoter in the presence of RNA polymerase. These findings suggest that DegU-P interacts with SlrR. In support of this hypothesis, disruption of the
slrR
gene resulted in decreased
degU
expression. This newly identified regulatory mechanism for
degU
is considered to be sequential transcription factor replacement.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
21 articles.
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