Affiliation:
1. Department of Microbiology, University of Iowa, Iowa City, Iowa 52242
Abstract
ABSTRACT
In
Escherichia coli
, the
gcvB
gene encodes a nontranslated RNA (referred to as GcvB) that regulates OppA and DppA, two periplasmic binding proteins for the oligopeptide and dipeptide transport systems. An additional regulatory target of GcvB,
sstT
, was found by microarray analysis of RNA isolated from a wild-type strain and a
gcvB
deletion strain grown to mid-log phase in Luria-Bertani broth. The SstT protein functions to transport
l
-serine and
l
-threonine by sodium transport into the cell. Reverse transcription-PCR and translational fusions confirmed that GcvB negatively regulates
sstT
mRNA levels in cells grown in Luria-Bertani broth. A series of transcriptional fusions identified a region of
sstT
mRNA upstream of the ribosome binding site needed for negative regulation by GcvB. Analysis of the GcvB RNA identified a sequence complementary to this region of the
sstT
mRNA. The region of GcvB complementary to
sstT
mRNA is the same region of GcvB identified to regulate the
dppA
and
oppA
mRNAs. Mutations predicted to disrupt base pairing between
sstT
mRNA and GcvB were made in
gcvB
, which resulted in the identification of a small region of GcvB necessary for negative regulation of
sstT-lacZ
. Additionally, the RNA chaperone protein Hfq was found to be necessary for GcvB to negatively regulate
sstT
-
lacZ
in Luria-Bertani broth and glucose minimal medium supplemented with glycine. The
sstT
mRNA is the first target found to be regulated by GcvB in glucose minimal medium supplemented with glycine.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
48 articles.
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