Human Molecular Genetics Advance Access originally published online on September 22, 2008
Human Molecular Genetics 2008 17(24):4036-4044; doi:10.1093/hmg/ddn306
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Dominant membrane uncoupling by mutant adenine nucleotide translocase in mitochondrial diseases
1 Department of Biochemistry and Molecular Biology, SUNY Upstate Medical University, Syracuse, New York, NY 13210, USA 2 Department of Molecular Biology, University of Texas Southwestern Medical Center at Dallas, Dallas, TX 75390-9148, USA
* To whom correspondence should be addressed at: Department of Biochemistry and Molecular Biology, SUNY Upstate Medical University, 750 East Adams Street, Syracuse, NY 13210, USA. Tel: +1 3154648723; Fax: +1 3154648750; Email: chenx{at}upstate.edu
Received August 15, 2008; Accepted September 17, 2008
Adenine nucleotide translocase (Ant) is the most abundant protein on the mitochondrial inner membrane (MIM) primarily involved in ADP/ATP exchange. Ant also possesses a discrete membrane uncoupling activity. Specific mis-sense mutations in the human Ant1 cause autosomal dominant Progressive External Ophthalmoplegia (adPEO), mitochondrial myopathy and cardiomyopathy, which are commonly manifested by fractional mitochondrial DNA (mtDNA) deletions. It is currently thought that the pathogenic mutations alter substrate preference (e.g. ATP versus ADP) thereby dominantly disturbing adenine nucleotide homeostasis in mitochondria. This may interfere with mtDNA replication, consequently affecting mtDNA stability and oxidative phosphorylation. Here, we showed that the adPEO-type A128P, A106D and M114P mutations in the yeast Aac2p share the following common dominant phenotypes: electron transport chain damage, intolerance to moderate over-expression, synthetic lethality with low 
m conditions, hypersensitivity to the uncoupler carbonyl cyanide m-chlorophenylhydrazone (CCCP) and mtDNA instability. More interestingly, the aac2A137D allele mimicking ant1A123D in mitochondrial myopathy and cardiomyopathy exhibits similar dominant phenotypes. Because Aac2A137D is known to completely lack transport activity, it is strongly argued that the dominant mitochondrial damages are not caused by aberrant nucleotide transport. The four pathogenic mutations occur in a structurally dynamic gating region on the cytosolic side. We provided direct evidence that the mutant alleles uncouple mitochondrial respiration. The pathogenic mutations likely enhance the intrinsic proton-conducting activity of Ant, which excessively uncouples the MIM thereby affecting energy transduction and mitochondrial biogenesis. mtDNA disintegration is a phenotype co-lateral to mitochondrial damages. These findings provide mechanistic insights into the pathogenesis of the Ant1-induced diseases.
CiteULike 
Connotea 
Del.icio.us What's this?
This article has been cited by other articles:
|
|
 |
|
  R. El-Khoury and A. Sainsard-Chanet Suppression of Mitochondrial DNA Instability of Autosomal Dominant Forms of Progressive External Ophthalmoplegia-Associated ANT1 Mutations in Podospora anserina Genetics, November 1, 2009; 183(3): 861 - 871. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
L. N. Dimitrov, R. B. Brem, L. Kruglyak, and D. E. Gottschling Polymorphisms in Multiple Genes Contribute to the Spontaneous Mitochondrial Genome Instability of Saccharomyces cerevisiae S288C Strains Genetics, September 1, 2009; 183(1): 365 - 383. [Abstract] [Full Text] [PDF]
|
|