4.5 Article

The par toxin-antitoxin system from Enterococcus faecalis plasmid pAD1 and its chromosomal homologs

Journal

RNA BIOLOGY
Volume 9, Issue 12, Pages 1498-1503

Publisher

TAYLOR & FRANCIS INC
DOI: 10.4161/rna.22311

Keywords

plasmid stability; post-segregational killing; peptide toxins; antisense RNA; toxin-antitoxin

Funding

  1. Public Health Service grant [GM55544]
  2. National Science Foundation Grant [MCB-9723098]
  3. Division of Basic Biomedical Sciences, Sanford School of Medicine

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The par post-segregational killing locus present on Enterococcus faecalis plasmid pAD1 was the first Type I toxin-antitoxin system described in Gram-positive bacteria. Translation of the 33 amino acid Fst toxin, encoded on RNA I, is suppressed by a 66 nucleotide regulatory RNA, RNA II. RNA I and RNA II are transcribed convergently and interact at dispersed regions of complementarity, establishing a stable complex that accumulates in plasmid-containing cells. RNA II is slowly removed from the complex, allowing translation of RNA I in plasmid-free segregants. Intramolecular structures are also important for regulating translation of RNA I. The Fst toxin contains a putative transmembrane domain and is believed to exert its function at the bacterial cytoplasmic membrane, although its precise target and mode of action have yet to be determined. Numerous chromosomal homologs of pAD1 par have been identified in Gram-positive bacteria suggesting that this locus may play important roles in cellular function.

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