Shy1 couples Cox1 translational regulation to cytochrome c oxidase assembly

被引:115
|
作者
Mick, David U.
Wagner, Karina
van der Laan, Martin
Frazier, Ann E.
Perschil, Inge
Pawlas, Magdalena
Meyer, Helmut E.
Warscheid, Bettina
Rehling, Peter
机构
[1] Univ Freiburg, Inst Biochem & Mol Biol, Zentrum Biochem & Mol Zellforsch, D-79104 Freiburg, Germany
[2] Univ Freiburg, Fak Biol, Freiburg, Germany
[3] La Trobe Univ, Dept Biochem, Melbourne, Vic, Australia
[4] Ruhr Univ Bochum, Med Proteom Ctr, D-4630 Bochum, Germany
来源
EMBO JOURNAL | 2007年 / 26卷 / 20期
关键词
Leigh syndrome; mitochondria; protein complex assembly; respiratory chain complex; SURF1;
D O I
10.1038/sj.emboj.7601862
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
Cytochrome c oxidase ( complex IV) of the respiratory chain is assembled from nuclear and mitochondrially-encoded subunits. Defects in the assembly process lead to severe human disorders such as Leigh syndrome. Shy1 is an assembly factor for complex IV in Saccharomyces cerevisiae and mutations of its human homolog, SURF1, are the most frequent cause for Leigh syndrome. We report that Shy1 promotes complex IV biogenesis through association with different protein modules; Shy1 interacts with Mss51 and Cox14, translational regulators of Cox1. Additionally, Shy1 associates with the subcomplexes of complex IV that are potential assembly intermediates. Formation of these subcomplexes depends on Coal (YIL157c), a novel assembly factor that cooperates with Shy1. Moreover, partially assembled forms of complex IV bound to Shy1 and Cox14 can associate with the bc1 complex to form transitional supercomplexes. We suggest that Shy1 links Cox1 translational regulation to complex IV assembly and supercomplex formation.
引用
收藏
页码:4347 / 4358
页数:12
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