Affiliation:
1. Wadsworth Center, New York State Department of Health, Center for Medical Sciences, Albany, New York
2. Department of Biophysics, The Johns Hopkins University, Baltimore, Maryland
Abstract
ABSTRACT
DsrA RNA is a small (87-nucleotide) regulatory RNA of
Escherichia coli
that acts by RNA-RNA interactions to control translation and turnover of specific mRNAs. Two targets of DsrA regulation are RpoS, the stationary-phase and stress response sigma factor (σ
s
), and H-NS, a histone-like nucleoid protein and global transcription repressor. Genes regulated globally by RpoS and H-NS include stress response proteins and virulence factors for pathogenic
E. coli
. Here, by using transcription profiling via DNA arrays, we have identified genes induced by DsrA. Steady-state levels of mRNAs from many genes increased with DsrA overproduction, including multiple acid resistance genes of
E. coli
. Quantitative primer extension analysis verified the induction of individual acid resistance genes in the
hdeAB
,
gadAX
, and
gadBC
operons.
E. coli
K-12 strains, as well as pathogenic
E. coli
O157:H7, exhibited compromised acid resistance in
dsrA
mutants. Conversely, overproduction of DsrA from a plasmid rendered the acid-sensitive
dsrA
mutant extremely acid resistant. Thus, DsrA RNA plays a regulatory role in acid resistance. Whether DsrA targets acid resistance genes directly by base pairing or indirectly via perturbation of RpoS and/or H-NS is not known, but in either event, our results suggest that DsrA RNA may enhance the virulence of pathogenic
E. coli
.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
75 articles.
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