Drosophila HtrA2 is dispensable for apoptosis but acts downstream of PINK1 independently from Parkin

被引:69
作者
Tain, L. S. [2 ,3 ]
Chowdhury, R. B. [1 ]
Tao, R. N. [3 ]
Plun-Favreau, H. [4 ,5 ]
Moisoi, N. [6 ]
Martins, L. M. [6 ]
Downward, J. [4 ]
Whitworth, A. J. [2 ,3 ]
Tapon, N. [1 ]
机构
[1] Canc Res UK, Apoptosis & Proliferat Control Lab, London Res Inst, London WC2A 3PX, England
[2] Univ Sheffield, MRC Ctr Dev & Biomed Genet, Sheffield S10 2TN, S Yorkshire, England
[3] Univ Sheffield, Dept Biomed Sci, Sheffield S10 2TN, S Yorkshire, England
[4] Canc Res UK, Signal Transduct Lab, London Res Inst, London WC2A 3PX, England
[5] UCL, Inst Neurol, Mol Neurosci Dept, London WC1N 3BG, England
[6] MRC Toxicol Unit, Cell Death Regulat Lab, Leicester LE1 9HN, Leics, England
基金
英国惠康基金;
关键词
HtrA2; Omi; PINK1; Parkinson's disease; Drosophila; apoptosis; mitochondria; SERINE-PROTEASE OMI/HTRA2; CELL-DEATH; MITOCHONDRIAL PATHOLOGY; CASPASE ACTIVITY; DISEASE; MUTANTS; INHIBITOR; PATHWAY; STRESS; OMI;
D O I
10.1038/cdd.2009.23
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
High temperature requirement A2 (HtrA2/Omi) is a mitochondrial protease that exhibits proapoptotic and cell-protective properties and has been linked to Parkinson's disease (PD). Impaired mitochondrial function is a common trait in PD patients, and is likely to play a significant role in pathogenesis of parkinsonism, but the molecular mechanisms remain poorly understood. Genetic studies in Drosophila have provided valuable insight into the function of other PD-linked genes, in particular PINK1 and parkin, and their role in maintaining mitochondrial integrity. Recently, HtrA2 was shown to be phosphorylated in a PINK1-dependent manner, suggesting it might act in the PINK1 pathway. Here, we describe the characterization of mutations in Drosophila HtrA2, and genetic analysis of its function with PINK1 and parkin. Interestingly, we find HtrA2 appears to be dispensable for developmental or stress-induced apoptosis. In addition, we found HtrA2 mutants share some phenotypic similarities with parkin and PINK1 mutants, suggesting that it may function in maintaining mitochondrial integrity. Our genetic interaction studies, including analysis of double-mutant combinations and epistasis experiments, suggest HtrA2 acts downstream of PINK1 but in a pathway parallel to Parkin. Cell Death and Differentiation (2009) 16, 1118-1125; doi:10.1038/cdd.2009.23; published online 13 March 2009
引用
收藏
页码:1118 / 1125
页数:8
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