Unraveling the complexity of mitochondrial complex I assembly: A dynamic process

被引:95
作者
Sanchez-Caballero, Laura [1 ]
Guerrero-Castillo, Sergio [1 ]
Nijtmans, Leo [1 ]
机构
[1] Radboud Univ Nijmegen, Med Ctr, Dept Pediat, Radboud Ctr Mitochondrial Med, Geert Grootepl Zuid 10, NL-6525 GA Nijmegen, Netherlands
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS | 2016年 / 1857卷 / 07期
关键词
Mitochondria; Mitochondrial disorders; Human complex I; Complex I assembly; Assembly factors; RESPIRATORY-CHAIN COMPLEXES; OXIDATIVE-PHOSPHORYLATION; NUBPL MUTATIONS; PRESEQUENCE TRANSLOCASE; PROTEIN TRANSLOCATION; MOLECULAR CHAPERONE; INTERMEMBRANE SPACE; CATALYTIC-ACTIVITY; ENCODED SUBUNITS; SKELETAL-MUSCLE;
D O I
10.1016/j.bbabio.2016.03.031
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
Mammalian complex I is composed of 44 different subunits and its assembly requires at least 13 specific assembly factors. Proper function of the mitochondrial respiratory chain enzyme is of crucial importance for cell survival due to its major participation in energy production and cell signaling. Complex I assembly depends on the coordination of several crucial processes that need to be tightly interconnected and orchestrated by a number of assembly factors. The understanding of complex I assembly evolved from simple sequential concept to the more sophisticated modular assembly model describing a convoluted process. According to this model, the different modules assemble independently and associate afterwards with each other to form the final enzyme. In this review, we aim to unravel the complexity of complex I assembly and provide the latest insights in this fundamental and fascinating process. This article is part of a Special Issue entitled Respiratory complex I, edited by Volker Zickermann and Ulrich Brandt. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:980 / 990
页数:11
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