Vidoni Sara, Harbour Michael E, Guerrero-Castillo Sergio, Signes Alba, Ding Shujing, Fearnley Ian M, Taylor Robert W, Tiranti Valeria, Arnold Susanne, Fernandez-Vizarra Erika, Zeviani Massimo
MRC Mitochondrial Biology Unit, Cambridge CB2 0XY, UK.
Radboud Center for Mitochondrial Medicine, Radboud University Medical Center, 6525 Nijmegen, the Netherlands.
Cell Rep. 2017 Feb 14;18(7):1727-1738. doi: 10.1016/j.celrep.2017.01.044.
The biogenesis of human cytochrome c oxidase (COX) is an intricate process in which three mitochondrial DNA (mtDNA)-encoded core subunits are assembled in a coordinated way with at least 11 nucleus-encoded subunits. Many chaperones shared between yeast and humans are involved in COX assembly. Here, we have used a MT-CO3 mutant cybrid cell line to define the composition of assembly intermediates and identify new human COX assembly factors. Quantitative mass spectrometry analysis led us to modify the assembly model from a sequential pathway to a module-based process. Each module contains one of the three core subunits, together with different ancillary components, including HIGD1A. By the same analysis, we identified the short isoform of the myofibrillogenesis regulator 1 (MR-1S) as a new COX assembly factor, which works with the highly conserved PET100 and PET117 chaperones to assist COX biogenesis in higher eukaryotes.
人类细胞色素c氧化酶(COX)的生物合成是一个复杂的过程,其中三个线粒体DNA(mtDNA)编码的核心亚基与至少11个核编码亚基以协调的方式组装在一起。酵母和人类共有的许多伴侣蛋白参与了COX的组装。在这里,我们使用了一种MT-CO3突变体胞质杂种细胞系来确定组装中间体的组成,并鉴定新的人类COX组装因子。定量质谱分析使我们将组装模型从顺序途径修改为基于模块的过程。每个模块包含三个核心亚基之一,以及不同的辅助成分,包括HIGD1A。通过同样的分析,我们鉴定出肌原纤维生成调节因子1的短异构体(MR-1S)是一种新的COX组装因子,它与高度保守的PET100和PET117伴侣蛋白协同作用,以协助高等真核生物中的COX生物合成。