The Ubiquitin-Proteasome System Regulates Mitochondrial Intermembrane Space Proteins

被引:107
|
作者
Bragoszewski, Piotr [1 ]
Gornicka, Agnieszka [1 ]
Sztolsztener, Malgorzata E. [1 ]
Chacinska, Agnieszka [1 ]
机构
[1] Int Inst Mol & Cell Biol, Warsaw, Poland
关键词
DISULFIDE RELAY SYSTEM; DEPENDENT DEGRADATION; PRECURSOR OXIDATION; MEMBRANE-PROTEINS; ELECTRON-TRANSFER; BOND FORMATION; IMPORT; MIA40; PATHWAY; ERV1;
D O I
10.1128/MCB.01579-12
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
Mitochondrial precursor proteins are synthesized in the cytosol and subsequently imported into mitochondria. The import of mitochondrial intermembrane space proteins is coupled with their oxidative folding and governed by the mitochondrial intermembrane space import and assembly (MIA) pathway. The cytosolic steps that precede mitochondrial import are not well understood. We identified a role for the ubiquitin-proteasome system in the biogenesis of intermembrane space proteins. Interestingly, the function of the ubiquitin-proteasome system is not restricted to conditions of mitochondrial protein import failure. The ubiquitin-proteasome system persistently removes a fraction of intermembrane space proteins under physiological conditions, acting as a negative regulator in the biogenesis of this class of proteins. Thus, the ubiquitin-proteasome system plays an important role in determining the levels of proteins targeted to the intermembrane space of mitochondria.
引用
收藏
页码:2136 / 2148
页数:13
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