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 CO2 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.

Highlights

  • Reversible protein phosphorylation is a mechanism for shortterm regulation of oxidative phosphorylation (OXPHOS) in mammalian mitochondria

  • We demonstrate that protein kinase A (PKA) and mitochondrial soluble adenylyl cyclase (mt-sAC) modulation induce reactive oxygen species (ROS)-mediated changes in the regulation of OXPHOS biogenesis that are different in Cytochrome oxidase (COX) deficient and wild type (WT) cells

  • We have demonstrated that OXPHOS regulation by mitochondrial PKA is different in normal and COX defective cells and tissues, in humans and mice

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Summary

Introduction

Reversible protein phosphorylation is a mechanism for shortterm regulation of oxidative phosphorylation (OXPHOS) in mammalian mitochondria. Mitochondria contain all the components for OXPHOS protein phosphorylation, including different families of kinases and phosphatases (Horbinski & Chu, 2005; Lu et al, 2007; Pagliarini & Dixon, 2006). The presence of both protein kinase A (PKA) (Pagliarini & Dixon, 2006; Thomson, 2002) and A kinaseanchoring proteins (AKAPs) (Feliciello et al, 2005; Lewitt et al, 2001) has been demonstrated in mammalian mitochondria. An important missing piece of the puzzle, which is currently being investigated, is the identity of the mitochondrial phosphatases needed to dephosphorylate PKA targets

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