Latrophilin is required for toxicity of black widow spider venom in Caenorhabditis elegans

Biochem J. 2004 Feb 15;378(Pt 1):185-91. doi: 10.1042/BJ20031213.

Abstract

Black widow spider venom (BWSV) kills Caenorhabditis elegans after injection owing to the presence of heat- and detergent-sensitive components, which are high-molecular-mass latrotoxins. A C. elegans homologue of latrophilin/CIRL (calcium-independent receptor for latrotoxin), B0457.1, was identified and shown to have five conserved domains. RNAi (RNA interference) of this gene rendered C. elegans resistant to BWSV, whereas RNAi for CYP37A1 or a neurexin I homologue, and a deletion mutant of the related B0286.2 gene, had no effect on BWSV toxicity. The latrophilin RNAi mutants exhibit changes in defaecation cycle and alterations in drug sensitivity. These results demonstrate that latrophilin mediates the toxicity of BWSV and provide evidence for a physiological function of this receptor.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Caenorhabditis elegans / anatomy & histology
  • Caenorhabditis elegans / drug effects*
  • Caenorhabditis elegans / genetics
  • Caenorhabditis elegans Proteins
  • Molecular Sequence Data
  • RNA Interference
  • Receptors, Peptide / genetics
  • Receptors, Peptide / physiology*
  • Spider Venoms / toxicity*

Substances

  • Caenorhabditis elegans Proteins
  • Receptors, Peptide
  • Spider Venoms
  • alpha-latrotoxin receptor
  • lat-1 protein, C elegans
  • black widow spider venom