生物
电子传递复合体Ⅰ
生物发生
线粒体DNA
蛋白质亚单位
线粒体
点突变
细胞生物学
线粒体生物发生
电子传输链
呼吸链
线粒体呼吸链
遗传学
计算生物学
基因
突变
生物化学
作者
Luke E. Formosa,Marris G. Dibley,David A. Stroud,Michael T. Ryan
标识
DOI:10.1016/j.semcdb.2017.08.011
摘要
Mitochondrial complex I is the primary entry point for electrons into the electron transport chain, required for the bulk of cellular ATP production via oxidative phosphorylation. Complex I consists of 45 subunits, which are encoded by both nuclear and mitochondrial DNA. Currently, at least 15 assembly factors are known to be required for the complete maturation of complex I. Mutations in the genes encoding subunits and assembly factors lead to complex I deficiency, which can manifest as mitochondrial disease. The current model of complex I assembly suggests that the enzyme is built by the association of a set of smaller intermediate modules containing specific conserved core subunits and additional accessory subunits. Each module must converge in a spatially and temporally orchestrated fashion to allow assembly of the mature holoenzyme to occur. This review outlines the current understanding of complex I biogenesis, with an emphasis on the assembly factors that facilitate the building of this architectural giant.
科研通智能强力驱动
Strongly Powered by AbleSci AI