Biogenesis and assembly of eukaryotic cytochrome c oxidase catalytic core

被引:171
作者
Soto, Ileana C. [1 ]
Fontanesi, Flavia [2 ]
Liu, Jingjing [1 ]
Barrientos, Antoni [1 ,2 ]
机构
[1] Univ Miami, Miller Sch Med, Dept Biochem & Mol Biol, Miami, FL 33136 USA
[2] Univ Miami, Miller Sch Med, Dept Neurol, Miami, FL 33136 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS | 2012年 / 1817卷 / 06期
关键词
Mitochondria; Cytochrome c oxidase; COX catalytic core; COX assembly; MITOCHONDRIAL-MEMBRANE SYSTEM; COX1; MESSENGER-RNA; SACCHAROMYCES-CEREVISIAE MITOCHONDRIA; PENTATRICOPEPTIDE REPEAT PROTEIN; TRANSLATIONAL ACTIVATOR PROTEINS; HEME A-FARNESYLTRANSFERASE; NUCLEAR GENE-PRODUCTS; INNER-MEMBRANE; GROUP-I; ELECTRON-TRANSFER;
D O I
10.1016/j.bbabio.2011.09.005
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
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. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:883 / 897
页数:15
相关论文
共 208 条
[1]   Crystal structure of yeast Sco1 [J].
Abajian, C ;
Rosenzweig, AC .
JOURNAL OF BIOLOGICAL INORGANIC CHEMISTRY, 2006, 11 (04) :459-466
[2]   Mutations in COX10 result in a defect in mitochondrial heme A biosynthesis and account for multiple, early-onset clinical phenotypes associated with isolated COX deficiency [J].
Antonicka, H ;
Leary, SC ;
Agar, JN ;
Horvath, R ;
Kennaway, NG ;
Harding, CO ;
Jaksch, M ;
Shoubridge, EA .
HUMAN MOLECULAR GENETICS, 2003, 12 (20) :2693-2702
[3]   Mutations in COX15 produce a defect in the mitochondrial heme biosynthetic pathway, causing early-onset fatal hypertrophic cardiomyopathy [J].
Antonicka, H ;
Mattman, A ;
Carlson, CG ;
Glerum, DM ;
Hoffbuhr, KC ;
Leary, SC ;
Kennaway, NG ;
Shoubridge, EA .
AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 72 (01) :101-114
[4]   Mitochondrial transcription and its regulation in mammalian cells [J].
Asin-Cayuela, Jordi ;
Gustafsson, Claes M. .
TRENDS IN BIOCHEMICAL SCIENCES, 2007, 32 (03) :111-117
[5]   Mitochondrial copper(I) transfer from Cox17 to Sco1 is coupled to electron transfer [J].
Banci, Lucia ;
Bertini, Ivano ;
Ciofi-Baffoni, Simone ;
Hadjiloi, Theodoros ;
Martinelli, Manuele ;
Palumaa, Peep .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (19) :6803-6808
[6]   A structural characterization of human SCO2 [J].
Banci, Lucia ;
Bertini, Ivano ;
Ciofi-Baffoni, Simone ;
Gerothanassis, Loannis P. ;
Leontari, Iliana ;
Martinelli, Manuele ;
Wang, Shenlin .
STRUCTURE, 2007, 15 (09) :1132-1140
[7]   A hint for the function of human Sco1 from different structures [J].
Banci, Lucia ;
Bertini, Ivano ;
Calderone, Vito ;
Ciofi-Baffoni, Simone ;
Mangani, Stefano ;
Martinelli, Manuele ;
Palumaa, Peep ;
Wang, Shenlin .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (23) :8595-8600
[8]   Cytochrome oxidase in health and disease [J].
Barrientos, A ;
Barros, MH ;
Valnot, I ;
Rötig, A ;
Rustin, P ;
Tzagoloff, A .
GENE, 2002, 286 (01) :53-63
[9]   Mss51p and Cox14p jointly regulate mitochondrial Cox1p expression in Saccharomyces cerevisiae [J].
Barrientos, A ;
Zambrano, A ;
Tzagoloff, A .
EMBO JOURNAL, 2004, 23 (17) :3472-3482
[10]   Shy1p is necessary for full expression of mitochondrial COX1 in the yeast model of Leigh's syndrome [J].
Barrientos, A ;
Korr, D ;
Tzagoloff, A .
EMBO JOURNAL, 2002, 21 (1-2) :43-52