Parkin negatively regulates JNK pathway in the dopaminergic neurons of Drosophila

Proc Natl Acad Sci U S A. 2005 Jul 19;102(29):10345-50. doi: 10.1073/pnas.0500346102. Epub 2005 Jul 7.

Abstract

Parkin, an E3 ubiquitin ligase, has been found to be responsible for autosomal recessive juvenile parkinsonism characterized primarily by selective loss of dopaminergic neurons with subsequent defects in movements. However, the molecular mechanisms underlying this neuron loss remain elusive. Here, we characterized Drosophila parkin loss-of-function mutants, which exhibit shrinkage of dopaminergic neurons with decreased tyrosine hydroxylase level and impaired locomotion. The behavioral defect of parkin mutant flies was partially restored by administering L-DOPA, and the dopamine level in the brains of parkin mutant flies was highly decreased. Intriguingly, we found that c-Jun N-terminal kinase (JNK) is strongly activated in the dopaminergic neurons of parkin mutants and that impaired dopaminergic neuron phenotypes are dependent on the activation of the JNK signaling pathway. In consistent with this, our epistatic analysis and mammalian cell studies showed that Parkin inhibits the JNK signaling pathway in an E3 activity-dependent manner. These results suggest that loss of Parkin function up-regulates the JNK signaling pathway, which may contribute to the vulnerability of dopaminergic neurons in Drosophila parkin mutants and perhaps autosomal recessive juvenile parkinsonism patients.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Blotting, Northern
  • Blotting, Western
  • Brain / metabolism*
  • COS Cells
  • Chlorocebus aethiops
  • Dopamine / metabolism
  • Drosophila
  • Drosophila Proteins / genetics*
  • Drosophila Proteins / metabolism
  • Histocytochemistry
  • Immunoenzyme Techniques
  • Immunoprecipitation
  • JNK Mitogen-Activated Protein Kinases / metabolism
  • Levodopa
  • MAP Kinase Kinase 4
  • Mitogen-Activated Protein Kinase Kinases / metabolism
  • Mutation / genetics
  • Neurons / metabolism*
  • Parkinsonian Disorders / genetics*
  • Parkinsonian Disorders / metabolism
  • Signal Transduction / physiology*
  • Tyrosine 3-Monooxygenase / metabolism
  • Ubiquitin-Protein Ligases

Substances

  • Drosophila Proteins
  • Levodopa
  • Tyrosine 3-Monooxygenase
  • Ubiquitin-Protein Ligases
  • JNK Mitogen-Activated Protein Kinases
  • MAP Kinase Kinase 4
  • Mitogen-Activated Protein Kinase Kinases
  • park protein, Drosophila
  • Dopamine