Mitochondrial dysfunction in Drosophila PINK1 mutants is complemented by parkin - PubMed (original) (raw)

. 2006 Jun 29;441(7097):1157-61.

doi: 10.1038/nature04788. Epub 2006 May 3.

• PMID: 16672980
• DOI: 10.1038/nature04788

Mitochondrial dysfunction in Drosophila PINK1 mutants is complemented by parkin

Jeehye Park et al. Nature. 2006.

Abstract

Autosomal recessive juvenile parkinsonism (AR-JP) is an early-onset form of Parkinson's disease characterized by motor disturbances and dopaminergic neurodegeneration. To address its underlying molecular pathogenesis, we generated and characterized loss-of-function mutants of Drosophila PTEN-induced putative kinase 1 (PINK1), a novel AR-JP-linked gene. Here, we show that PINK1 mutants exhibit indirect flight muscle and dopaminergic neuronal degeneration accompanied by locomotive defects. Furthermore, transmission electron microscopy analysis and a rescue experiment with Drosophila Bcl-2 demonstrated that mitochondrial dysfunction accounts for the degenerative changes in all phenotypes of PINK1 mutants. Notably, we also found that PINK1 mutants share marked phenotypic similarities with parkin mutants. Transgenic expression of Parkin markedly ameliorated all PINK1 loss-of-function phenotypes, but not vice versa, suggesting that Parkin functions downstream of PINK1. Taken together, our genetic evidence clearly establishes that Parkin and PINK1 act in a common pathway in maintaining mitochondrial integrity and function in both muscles and dopaminergic neurons.

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Comment in

• Neurodegenerative disease: pink, parkin and the brain.
  Pallanck L, Greenamyre JT. Pallanck L, et al. Nature. 2006 Jun 29;441(7097):1058. doi: 10.1038/4411058a. Nature. 2006. PMID: 16810237 No abstract available.

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