Modulation of mitochondrial protein phosphorylation by soluble adenylyl cyclase ameliorates cytochrome oxidase defects

EMBO Mol Med. 2009 Nov;1(8-9):392-406. doi: 10.1002/emmm.200900046.

Abstract

Phosphorylation of respiratory chain components has emerged as a mode of regulation of mitochondrial energy metabolism, but its mechanisms are still largely unexplored. A recently discovered intramitochondrial signalling pathway links CO(2) generated by the Krebs cycle with the respiratory chain, through the action of a mitochondrial soluble adenylyl cyclase (mt-sAC). Cytochrome oxidase (COX), whose deficiency causes a number of fatal metabolic disorders, is a key mitochondrial enzyme activated by mt-sAC. We have now discovered that the mt-sAC pathway modulates mitochondrial biogenesis in a reactive oxygen species dependent manner, in cultured cells and in animals with COX deficiency. We show that upregulation of mt-sAC normalizes reactive oxygen species production and mitochondrial biogenesis, thereby restoring mitochondrial function. This is the first example of manipulation of a mitochondrial signalling pathway to achieve a direct positive modulation of COX, with clear implications for the development of novel approaches to treat mitochondrial diseases.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenylyl Cyclases / genetics
  • Adenylyl Cyclases / metabolism*
  • Animals
  • Cell Line
  • Cyclic AMP-Dependent Protein Kinases / metabolism
  • DNA, Mitochondrial / genetics
  • Electron Transport Complex IV / genetics
  • Electron Transport Complex IV / metabolism*
  • Gene Deletion
  • Gene Expression Regulation*
  • Humans
  • Mice
  • Mitochondria / enzymology*
  • Mitochondria / pathology
  • Mitochondrial Diseases / enzymology
  • Mitochondrial Diseases / genetics
  • Mutation
  • Oxidative Phosphorylation
  • Reactive Oxygen Species / metabolism
  • Trans-Activators / genetics
  • Trans-Activators / metabolism

Substances

  • DNA, Mitochondrial
  • Reactive Oxygen Species
  • Trans-Activators
  • Electron Transport Complex IV
  • Cyclic AMP-Dependent Protein Kinases
  • Adenylyl Cyclases