Affiliation:
1. Department of Microbiology, Dartmouth Medical School, Hanover, New Hampshire 03755
Abstract
ABSTRACT
The expression of protein A (
spa
) is repressed by global regulatory loci
sarA
and
agr
. Although SarA may directly bind to the
spa
promoter to downregulate
spa
expression, the mechanism by which
agr
represses
spa
expression is not clearly understood. In searching for SarA homologs in the partially released genome, we found a SarA homolog, encoding a 250-amino-acid protein designated SarS, upstream of the
spa
gene. The expression of
sarS
was almost undetectable in parental strain RN6390 but was highly expressed in
agr
and
sarA
mutants, strains normally expressing high level of protein A. Interestingly, protein A expression was decreased in a
sarS
mutant as detected in an immunoblot but returned to near-parental levels in a complemented
sarS
mutant. Transcriptional fusion studies with a 158- and a 491-bp
spa
promoter fragment linked to the
xylE
reporter gene disclosed that the transcription of the
spa
promoter was also downregulated in the
sarS
mutant compared with the parental strain. Interestingly, the enhancement in
spa
expression in an
agr
mutant returned to a near-parental level in the
agr sarS
double mutant but not in the
sarA sarS
double mutant. Correlating with this divergent finding is the observation that enhanced
sarS
expression in an
agr
mutant was repressed by the
sarA
locus supplied in
trans
but not in a
sarA
mutant expressing RNAIII from a plasmid. Gel shift studies also revealed the specific binding of SarS to the 158-bp
spa
promoter. Taken together, these data indicated that the
agr
locus probably mediates
spa
repression by suppressing the transcription of
sarS
, an activator of
spa
expression. However, the pathway by which the
sarA
locus downregulates
spa
expression is
sarS
independent.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Immunology,Microbiology,Parasitology
Cited by
98 articles.
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