Y. Kagawa et al., Regulation of energy metabolism in human cells in aging and diabetes: FoF(1), mtDNA, UCP, and ROS, BIOC BIOP R, 266(3), 1999, pp. 662-676
Citations number
138
Categorie Soggetti
Biochemistry & Biophysics
Journal title
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
Recent advances in bioenergetics consist of discoveries related to rotation
al coupling in ATP synthase (FoF(1)), uncoupling proteins (UGP), reactive o
xygen species (ROS) and mitochondrial DNA (mtDNA). As shown in cloned sheep
, mammalian genomes are composed of both nuclear DNA (nDNA) and maternal mt
DNA. Oxidative phosphorylation (oxphos) varies greatly depending on cellula
r activities, and is regulated by both gene expression and the electrochemi
cal potential difference of H+ (Delta mu H+) The expression of both mtDNA (
by mtTFA) and nDNA for oxphos and UCP (by NRFs, etc.) is coordinated by a f
actor called PGC-1. The Delta mu H+ rotates an axis in FoF(1) that is regul
ated by inhibitors and ATP-sensitive K+-channels.