Insulin/Insulin-like growth factor signaling controls non-Dauer developmental speed in the nematode Caenorhabditis elegans

Genetics. 2011 Jan;187(1):337-43. doi: 10.1534/genetics.110.123323. Epub 2010 Oct 13.

Abstract

Identified as a major pathway controlling entry in the facultative dauer diapause stage, the DAF-2/Insulin receptor (InsR) signaling acts in multiple developmental and physiological regulation events in Caenorhabditis elegans. Here we identified a role of the insulin-like pathway in controlling developmental speed during the C. elegans second larval stage. This role relies on the canonical DAF-16/FOXO-dependent branch of the insulin-like signaling and is largely independent of dauer formation. Our studies provide further evidence for broad conservation of insulin/insulin-like growth factor (IGF) functions in developmental speed control.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Animals
  • Caenorhabditis elegans / cytology*
  • Caenorhabditis elegans / drug effects
  • Caenorhabditis elegans / growth & development*
  • Caenorhabditis elegans / metabolism
  • Caenorhabditis elegans Proteins / genetics
  • Caenorhabditis elegans Proteins / metabolism*
  • Dimethylphenylpiperazinium Iodide / pharmacology
  • Forkhead Transcription Factors
  • Insulin / metabolism*
  • Larva / drug effects
  • Larva / growth & development
  • Larva / metabolism
  • Receptor, Insulin / genetics
  • Receptor, Insulin / metabolism
  • Signal Transduction* / drug effects
  • Somatomedins / metabolism*
  • Time Factors
  • Transcription Factors / metabolism

Substances

  • Caenorhabditis elegans Proteins
  • Forkhead Transcription Factors
  • Insulin
  • Somatomedins
  • Transcription Factors
  • daf-16 protein, C elegans
  • Dimethylphenylpiperazinium Iodide
  • DAF-2 protein, C elegans
  • Receptor, Insulin