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Gene Review

ssrA  -  miscRNA

Escherichia coli O157:H7 str. EDL933

 
 
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Disease relevance of ssrA

  • In E. coli, the adaptor SspB tethers ssrA-tagged substrates to the ClpXP protease, causing a modest increase in their rate of degradation [1].
  • The PAI is 39.5 kb in size, has low %G+C (35%), contains putative integrase and transposase genes, is flanked by att sites, and inserts near a 10Sa RNA gene (ssrA), suggesting it may be of bacteriophage origin [2].
  • Excision and loss of the cryptic prophage apparently allow expression of the Alp protease by inactivating a small stable RNA (10Sa RNA) encoded by the ssrA gene [3].
 

High impact information on ssrA

  • Although A-site-cleaved mRNAs were not detected, tmRNA-mediated ssrA tagging after SecM glycine 165 was observed [4].
  • Indeed, compensatory overexpression of tRNA(2)(Pro) readily inhibits ssrA tagging after glycine 165, but has no effect on the duration of SecM ribosome arrest [4].
  • Inactivation of ssrA by insertional mutagenesis is sufficient to allow expression of the suppressing Alp protease, even in the presence of the cryptic prophage [3].

References

  1. Engineering controllable protein degradation. McGinness, K.E., Baker, T.A., Sauer, R.T. Mol. Cell (2006) [Pubmed]
  2. A Vibrio cholerae pathogenicity island associated with epidemic and pandemic strains. Karaolis, D.K., Johnson, J.A., Bailey, C.C., Boedeker, E.C., Kaper, J.B., Reeves, P.R. Proc. Natl. Acad. Sci. U.S.A. (1998) [Pubmed]
  3. Excision of a P4-like cryptic prophage leads to Alp protease expression in Escherichia coli. Kirby, J.E., Trempy, J.E., Gottesman, S. J. Bacteriol. (1994) [Pubmed]
  4. Prolyl-tRNAPro in the A-site of SecM-arrested Ribosomes Inhibits the Recruitment of Transfer-messenger RNA. Garza-S??nchez, F., Janssen, B.D., Hayes, C.S. J. Biol. Chem. (2006) [Pubmed]
 
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