• Media type: E-Article
  • Title: Early termination of the Shiga toxin transcript generates a regulatory small RNA
  • Contributor: Sy, Brandon M.; Lan, Ruiting; Tree, Jai J.
  • imprint: Proceedings of the National Academy of Sciences, 2020
  • Published in: Proceedings of the National Academy of Sciences
  • Language: English
  • DOI: 10.1073/pnas.2006730117
  • ISSN: 0027-8424; 1091-6490
  • Keywords: Multidisciplinary
  • Origination:
  • Footnote:
  • Description: <jats:title>Significance</jats:title> <jats:p> Enterohemorrhagic <jats:italic>E. coli</jats:italic> is a significant human pathogen that can cause severe disease due to the release of Shiga toxins. The toxins are encoded within lysogenic bacteriophage and controlled by antitermination of the phage late promoter, P <jats:sub>R′</jats:sub> . This promoter is always active, but terminated immediately downstream during lysogeny. A byproduct of antitermination regulation is transcription of a short RNA that is thought to be nonfunctional. Here we demonstrate that in Shiga toxin-encoding phages, this short RNA is a Hfq-binding regulatory small RNA. The small RNA represses toxin production threefold under lysogenic conditions and promotes high cell density growth. Lysogenic bacteriophages are highly abundant and our results suggest that antiterminated phage promoters may be a rich source of regulatory RNAs. </jats:p>
  • Access State: Open Access