Bacterial death induced by expression of the intracellular portion of human Fas

Cell Death Differ. 1999 Aug;6(8):805-12. doi: 10.1038/sj.cdd.4400555.

Abstract

In attempting to produce the intracellular portion of human Fas (IC175 - 319) as a GST-fusion protein we found that expression of GST-IC175 - 319, but not GST alone or GST-IC231 - 298 (containing the Fas death domain), rapidly caused the death of host E. coli cells. Expression of GST-IC175 - 319 with a single amino acid substitution (V238N) corresponding to the mouse lprcg mutation, or E245A, which abolishes the ability of Fas to self-associate, did not kill bacteria. Deletional analysis identified a 20-amino acids region (Asp210 - Lys230) as essential for the killing activity, and introduction of a single amino acid substitution (T225P) in this 20 amino acid region markedly decreased the ability of Fas- IC175 - 319 to cause bacterial death. These data indicate that Fas can deliver a death signal in prokaryotic organisms by a means that shares some features with eukaryotic cells, and raise the possibility that certain mechanisms leading to programmed cell death may be conserved from bacteria to mammalian cells.

MeSH terms

  • Animals
  • Binding Sites
  • Escherichia coli*
  • Humans
  • Intracellular Fluid
  • Mice
  • Point Mutation
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / pharmacology
  • fas Receptor / genetics
  • fas Receptor / pharmacology*

Substances

  • Recombinant Fusion Proteins
  • fas Receptor