Tom70 Is Essential for PINK1 Import into Mitochondria

被引:49
|
作者
Kato, Hiroki [1 ]
Lu, Qiping [1 ]
Rapaport, Doron [1 ]
Kozjak-Pavlovic, Vera [2 ]
机构
[1] Univ Tubingen, Interfac Inst Biochem, Tubingen, Germany
[2] Univ Wurzburg, Dept Microbiol, Bioctr, D-97070 Wurzburg, Germany
来源
PLOS ONE | 2013年 / 8卷 / 03期
关键词
OUTER-MEMBRANE PROTEINS; PARKINSONS-DISEASE; INTRACELLULAR MEMBRANES; QUALITY-CONTROL; PATHWAY; RECRUITMENT; BIOGENESIS; MECHANISMS; COMPLEX; BINDING;
D O I
10.1371/journal.pone.0058435
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
PTEN induced kinase 1 (PINK1) is a serine/threonine kinase in the outer membrane of mitochondria (OMM), and known as a responsible gene of Parkinson's disease (PD). The precursor of PINK1 is synthesized in the cytosol and then imported into the mitochondria via the translocase of the OMM (TOM) complex. However, a large part of PINK1 import mechanism remains unclear. In this study, we examined using cell-free system the mechanism by which PINK1 is targeted to and assembled into mitochondria. Surprisingly, the main component of the import channel, Tom40 was not necessary for PINK1 import. Furthermore, we revealed that the import receptor Tom70 is essential for PINK1 import. In addition, we observed that although PINK1 has predicted mitochondrial targeting signal, it was not processed by the mitochondrial processing peptidase. Thus, our results suggest that PINK1 is imported into mitochondria by a unique pathway that is independent of the TOM core complex but crucially depends on the import receptor Tom70.
引用
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页数:6
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