Mick David U, Wagner Karina, van der Laan Martin, Frazier Ann E, Perschil Inge, Pawlas Magdalena, Meyer Helmut E, Warscheid Bettina, Rehling Peter
Institut für Biochemie und Molekularbiologie, Zentrum für Biochemie und Molekulare Zellforschung, Universität Freiburg, Freiburg, Germany.
EMBO J. 2007 Oct 17;26(20):4347-58. doi: 10.1038/sj.emboj.7601862. Epub 2007 Sep 20.
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 Coa1 (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.
呼吸链中的细胞色素c氧化酶(复合体IV)由细胞核和线粒体编码的亚基组装而成。组装过程中的缺陷会导致严重的人类疾病,如 Leigh 综合征。Shy1 是酿酒酵母中复合体IV的组装因子,其人类同源物 SURF1 的突变是 Leigh 综合征最常见的病因。我们报告称,Shy1 通过与不同的蛋白质模块结合来促进复合体IV的生物合成;Shy1 与 Cox1 的翻译调节因子 Mss51 和 Cox14 相互作用。此外,Shy1 与复合体IV的潜在组装中间体亚复合体结合。这些亚复合体的形成依赖于与 Shy1 协同作用的新型组装因子 Coa1(YIL157c)。此外,与 Shy1 和 Cox14 结合的复合体IV的部分组装形式可与bc1复合体结合形成过渡性超级复合体。我们认为,Shy1 将 Cox1 的翻译调节与复合体IV的组装和超级复合体形成联系起来。