Requirement for a conserved Toll/interleukin-1 resistance domain protein in the Caenorhabditis elegans immune response

Proc Natl Acad Sci U S A. 2004 Apr 27;101(17):6593-8. doi: 10.1073/pnas.0308625101.

Abstract

The p38 mitogen-activated protein kinase pathway regulates innate immune responses in evolutionarily diverse species. We have previously shown that the Caenorhabditis elegans p38 mitogen-activated protein kinase, PMK-1, functions in an innate immune response pathway that mediates resistance to a variety of microbial pathogens. Here, we show that tir-1, a gene encoding a highly conserved Toll/IL-1 resistance (TIR) domain protein, is also required for C. elegans resistance to microbial pathogens. RNA interference inactivation of tir-1 resulted in enhanced susceptibility to killing by pathogens and correspondingly diminished PMK-1 phosphorylation. Unlike all known TIR-domain adapter proteins, overexpression of the human TIR-1 homologue, SARM, in mammalian cells was not sufficient to induce expression of NF-kappaB or IRF3-dependent reporter genes that are activated by Toll-like receptor signaling. These data reveal the involvement of a previously uncharacterized, evolutionarily conserved TIR domain protein in innate immunity that is functionally distinct from other known TIR domain signaling adapters.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Base Sequence
  • Caenorhabditis elegans / genetics
  • Caenorhabditis elegans / immunology*
  • DNA Primers
  • Enzyme Activation
  • Gene Expression Regulation
  • Membrane Glycoproteins / genetics
  • Membrane Glycoproteins / physiology*
  • Mitogen-Activated Protein Kinases / metabolism
  • Receptors, Interleukin-1 / genetics
  • Receptors, Interleukin-1 / physiology*
  • Signal Transduction
  • p38 Mitogen-Activated Protein Kinases

Substances

  • DNA Primers
  • Membrane Glycoproteins
  • Receptors, Interleukin-1
  • Mitogen-Activated Protein Kinases
  • p38 Mitogen-Activated Protein Kinases