4.8 Article

Identification of Bacteriophage-Encoded Anti-sRNAs in Pathogenic Escherichia coli

Journal

MOLECULAR CELL
Volume 55, Issue 2, Pages 199-213

Publisher

CELL PRESS
DOI: 10.1016/j.molcel.2014.05.006

Keywords

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Funding

  1. Wellcome Trust [WT090231MA, 092076]
  2. BBSRC Institute
  3. Biotechnology and Biological Sciences Research Council [BBS/E/D/20231761] Funding Source: researchfish
  4. BBSRC [BBS/E/D/20231761] Funding Source: UKRI

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In bacteria, Hfq is a core RNA chaperone that catalyzes the interaction of mRNAs with regulatory small RNAs (sRNAs). To determine in vivo RNA sequence requirements for Hfq interactions, and to study riboregulation in a bacterial pathogen, Hfq was UV crosslinked to RNAs in enterohemorrhagic Escherichia coli (EHEC). Hfq bound repeated trinucleotide motifs of A-R-N (A-A/G-any nucleotide) often associated with the Shine-Dalgarno translation initiation sequence in mRNAs. These motifs overlapped or were adjacent to the mRNA sequences bound by sRNAs. In consequence, sRNA-mRNA duplex formation will displace Hfq, promoting recycling. Fifty-five sRNAs were identified within bacteriophage-derived regions of the EHEC genome, including some of the most abundant Hfq-interacting sRNAs. One of these (AgvB) antagonized the function of the core genome regulatory sRNA, GcvB, by mimicking its mRNA substrate sequence. This bacteriophage-encoded anti-sRNA provided EHEC with a growth advantage specifically in bovine rectal mucus recovered from its primary colonization site in cattle.

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