MRC Mitochondrial Biology Unit, University of Cambridge, Cambridge, U.K.
Essays Biochem. 2018 Jul 20;62(3):309-320. doi: 10.1042/EBC20170102.
Mitochondria are the major source of ATP in the cell. Five multi-subunit complexes in the inner membrane of the organelle are involved in the oxidative phosphorylation required for ATP production. Thirteen subunits of these complexes are encoded by the mitochondrial genome often referred to as mtDNA. For this reason, the expression of mtDNA is vital for the assembly and functioning of the oxidative phosphorylation complexes. Defects of the mechanisms regulating mtDNA gene expression have been associated with deficiencies in assembly of these complexes, resulting in mitochondrial diseases. Recently, numerous factors involved in these processes have been identified and characterized leading to a deeper understanding of the mechanisms that underlie mitochondrial diseases.
线粒体是细胞中 ATP 的主要来源。细胞器内膜中的五个多亚基复合物参与了产生 ATP 所需的氧化磷酸化。这些复合物的 13 个亚基由线粒体基因组编码,通常称为 mtDNA。因此,mtDNA 的表达对于氧化磷酸化复合物的组装和功能至关重要。调节 mtDNA 基因表达的机制缺陷与这些复合物的组装缺陷有关,导致线粒体疾病。最近,已经鉴定和表征了许多参与这些过程的因素,这导致了对线粒体疾病基础机制的更深入理解。