Soto Ileana C, Fontanesi Flavia, Liu Jingjing, Barrientos Antoni
Department of Biochemistry & Molecular Biology, University of Miami Miller School of Medicine, Miami, FL 33136, USA.
Biochim Biophys Acta. 2012 Jun;1817(6):883-97. doi: 10.1016/j.bbabio.2011.09.005. Epub 2011 Sep 16.
Eukaryotic cytochrome c oxidase (COX) is the terminal enzyme of the mitochondrial respiratory chain. COX is a multimeric enzyme formed by subunits of dual genetic origin which assembly is intricate and highly regulated. The COX catalytic core is formed by three mitochondrial DNA encoded subunits, Cox1, Cox2 and Cox3, conserved in the bacterial enzyme. Their biogenesis requires the action of messenger-specific and subunit-specific factors which facilitate the synthesis, membrane insertion, maturation or assembly of the core subunits. The study of yeast strains and human cell lines from patients carrying mutations in structural subunits and COX assembly factors has been invaluable to identify these ancillary factors. Here we review the current state of knowledge of the biogenesis and assembly of the eukaryotic COX catalytic core and discuss the degree of conservation of the players and mechanisms operating from yeast to human. This article is part of a Special Issue entitled: Biogenesis/Assembly of Respiratory Enzyme Complexes.
真核细胞细胞色素c氧化酶(COX)是线粒体呼吸链的末端酶。COX是一种多聚体酶,由双重遗传起源的亚基组成,其组装过程复杂且受到高度调控。COX催化核心由三个线粒体DNA编码的亚基Cox1、Cox2和Cox3组成,这些亚基在细菌酶中是保守的。它们的生物合成需要信使特异性和亚基特异性因子的作用,这些因子促进核心亚基的合成、膜插入、成熟或组装。对携带结构亚基和COX组装因子突变的患者的酵母菌株和人类细胞系的研究,对于识别这些辅助因子具有重要价值。在这里,我们综述了真核COX催化核心生物合成和组装的当前知识状态,并讨论了从酵母到人类的相关作用因子和作用机制的保守程度。本文是名为“呼吸酶复合物的生物合成/组装”的特刊的一部分。