Originally published as Genetics Published Articles Ahead of Print on August 17, 2009.

Genetics, Vol. 183, 861-871, November 2009, Copyright © 2009
doi:10.1534/genetics.109.107813

Suppression of Mitochondrial DNA Instability of Autosomal Dominant Forms of Progressive External Ophthalmoplegia-Associated ANT1 Mutations in Podospora anserina

Riyad El-Khoury* and Annie Sainsard-Chanet*,{dagger},1

* Centre National de la Recherche Scientifique (CNRS), Centre de Génétique Moléculaire, Gif-sur-Yvette F-91198, France and {dagger} Université Paris-Sud, Orsay F-91405, France

1 Corresponding author: Centre de Génétique Moléculaire du CNRS, Allée de la Terrasse, Gif-sur-Yvette F-91198, France.
E-mail: annie.sainsard{at}cgm.cnrs-gif.fr

Maintenance and expression of mitochondrial DNA (mtDNA) are essential for the cell and the organism. In humans, several mutations in the adenine nucleotide translocase gene ANT1 are associated with multiple mtDNA deletions and autosomal dominant forms of progressive external ophthalmoplegia (adPEO). The mechanisms underlying the mtDNA instability are still obscure. A current hypothesis proposes that these pathogenic mutations primarily uncouple the mitochondrial inner membrane, which secondarily causes mtDNA instability. Here we show that the three adPEO-associated mutations equivalent to A114P, L98P, and V289M introduced into the Podospora anserina ANT1 ortholog dominantly cause severe growth defects, decreased reactive oxygen species production (ROS), decreased mitochondrial inner membrane potential ({Delta}{psi}), and accumulation of large-scale mtDNA deletions leading to premature death. Interestingly, we show that, at least for the adPEO-type M106P and A121P mutant alleles, the associated mtDNA instability cannot be attributed only to a reduced membrane potential or to an increased ROS level since it can be suppressed without restoration of the {Delta}{psi} or modification of the ROS production. Suppression of mtDNA instability due to the M106P and A121P mutations was obtained by an allele of the rmp1 gene involved in nucleo-mitochondrial cross- talk and also by an allele of the AS1 gene encoding a cytosolic ribosomal protein. In contrast, the mtDNA instability caused by the S296M mutation was not suppressed by these alleles.