4.4 Article

sigma(E) regulates and is regulated by a small RNA in Escherichia coli

Journal

JOURNAL OF BACTERIOLOGY
Volume 189, Issue 11, Pages 4243-4256

Publisher

AMER SOC MICROBIOLOGY
DOI: 10.1128/JB.00020-07

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Funding

  1. Intramural NIH HHS Funding Source: Medline
  2. NATIONAL CANCER INSTITUTE [Z01BC008714, ZIABC008714] Funding Source: NIH RePORTER

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RybB is a small, Hfq-binding noncoding RNA originally identified in a screen of conserved intergenic regions in Escherichia coli. Fusions of the rybB promoter to lacZ were used to screen plasmid genomic libraries and genomic transposon mutants for regulators of rybB expression. A number of plasmids, including some carrying rybB, negatively regulated the fusion. An insertion in the rep helicase and one upstream of dnaK decreased expression of the fusion. Multicopy suppressors of these insertions led to identification of two plasmids that stimulated the fusion. One contained the gene for the response regulator OmpR; the second contained mipA, encoding a murein hydrolase. The involvement of MipA and OmpR in cell surface synthesis suggested that the rybB promoter might be dependent on sigma(E). The sequence upstream of the +1 of rybB contains a consensus sigma(E) promoter. The activity of rybB-lacZ was increased in cells lacking the RseA anti-sigma factor and when sigma(E) was overproduced from a heterologous promoter. The activity of rybB-1acZ and the detection of RybB were totally abolished in an rpoE-null strain. In vitro, sigma(E) efficiently transcribes from this promoter. Both a rybB mutation and an hfq mutation significantly increased expression of both rybB-1acZ and rpoE-lacZ fusions, consistent with negative regulation of the alpha(E) response by RybB and other small RNAs. Based on the plasmid screens, NsrR, a repressor sensitive to nitric oxide, was also found to negatively regulate sigma(E)-dependent promoters in an RseA-independent fashion.

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