The MAP kinase JNK-1 of Caenorhabditis elegans: location, activation, and influences over temperature-dependent insulin-like signaling, stress responses, and fitness

J Cell Physiol. 2008 Mar;214(3):721-9. doi: 10.1002/jcp.21269.

Abstract

The mitogen-activated protein kinase (MAPK) pathways and insulin-like signaling play pivotal roles in cellular stress response. Using an anti-phospho-SAPK/JNK antibody and a daf-16::GFP-based reporter assay, the present study shows in Caenorhabditis elegans that ambient temperature (1-37 degrees C) specifically influences the activation (phosphorylation) of the MAP kinase JNK-1 as well as the nuclear translocation of DAF-16, the main downstream target of insulin-like signaling. Activated JNK-1 was detected only in neuronal cells, and JNK-1 was found to be controlled by the MAPK JKK-1 under heat stress. Comparative analyses on the wildtype and a jnk-1 deletion mutant revealed a promoting influence of JNK-1 on both nuclear DAF-16 translocations and DAF-16 target gene (superoxide dismutase 3, sod-3) expressions within peripheral, non-neuronal tissue. Consequently, the mutant exhibited a reduced thermal tolerance and reproductive fitness at higher temperatures. These results provide evidence of indirect interactions between neuronal MAPK and peripheral insulin-like signaling in response to environmental stimuli (temperature, H2O2).

MeSH terms

  • Animals
  • Caenorhabditis elegans / cytology
  • Caenorhabditis elegans / drug effects
  • Caenorhabditis elegans / enzymology*
  • Caenorhabditis elegans / physiology*
  • Caenorhabditis elegans Proteins / metabolism*
  • Cell Nucleus / drug effects
  • Cell Nucleus / enzymology
  • Enzyme Activation / drug effects
  • Forkhead Transcription Factors
  • Gene Deletion
  • Hydrogen Peroxide / pharmacology
  • Insulin / metabolism*
  • Intestines / cytology
  • Intestines / drug effects
  • Intestines / enzymology
  • Isoenzymes / metabolism
  • Mitogen-Activated Protein Kinases / metabolism*
  • Protein Transport / drug effects
  • Reproduction / drug effects
  • Signal Transduction* / drug effects
  • Superoxide Dismutase / metabolism
  • Temperature*
  • Transcription Factors / metabolism

Substances

  • Caenorhabditis elegans Proteins
  • Forkhead Transcription Factors
  • Insulin
  • Isoenzymes
  • Transcription Factors
  • daf-16 protein, C elegans
  • Hydrogen Peroxide
  • Superoxide Dismutase
  • JNK-1 protein, C elegans
  • Mitogen-Activated Protein Kinases