Regulation of DAF-2 receptor signaling by human insulin and ins-1, a member of the unusually large and diverse C. elegans insulin gene family

Genes Dev. 2001 Mar 15;15(6):672-86. doi: 10.1101/gad.867301.

Abstract

The activity of the DAF-2 insulin-like receptor is required for Caenorhabditis elegans reproductive growth and normal adult life span. Informatic analysis identified 37 C. elegans genes predicted to encode insulin-like peptides. Many of these genes are divergent insulin superfamily members, and many are clustered, indicating recent diversification of the family. The ins genes are primarily expressed in neurons, including sensory neurons, a subset of which are required for reproductive development. Structural predictions and likely C-peptide cleavage sites typical of mammalian insulins suggest that ins-1 is most closely related to insulin. Overexpression of ins-1, or expression of human insulin under the control of ins-1 regulatory sequences, causes partially penetrant arrest at the dauer stage and enhances dauer arrest in weak daf-2 mutants, suggesting that INS-1 and human insulin antagonize DAF-2 insulin-like signaling. A deletion of the ins-1 coding region does not enhance or suppress dauer arrest, indicating a functional redundancy among the 37 ins genes. Of five other ins genes tested, the only other one bearing a predicted C peptide also antagonizes daf-2 signaling, whereas four ins genes without a C peptide do not, indicating functional diversity within the ins family.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Animals, Genetically Modified
  • Caenorhabditis elegans / metabolism*
  • Caenorhabditis elegans Proteins*
  • Cloning, Molecular
  • Enhancer Elements, Genetic
  • Gene Deletion
  • Helminth Proteins / chemistry
  • Helminth Proteins / genetics*
  • Helminth Proteins / metabolism
  • Humans
  • Insulin / chemistry
  • Insulin / genetics*
  • Insulin / metabolism
  • Insulin / pharmacology*
  • Microscopy, Fluorescence
  • Models, Genetic
  • Molecular Sequence Data
  • Mutation
  • Phenotype
  • Promoter Regions, Genetic
  • Protein Structure, Tertiary
  • Receptor, Insulin / metabolism*
  • Recombinant Fusion Proteins / metabolism
  • Sequence Homology, Amino Acid
  • Signal Transduction*
  • Temperature
  • Time Factors

Substances

  • Caenorhabditis elegans Proteins
  • Helminth Proteins
  • Insulin
  • Recombinant Fusion Proteins
  • ins-1 protein, C elegans
  • DAF-2 protein, C elegans
  • Receptor, Insulin