Identification of an X-chromosomal locus and haplotype modulating the phenotype of a mitochondrial DNA disorder.
Hudson G,
Keers S,
Yu Wai Man P,
Griffiths P,
Huoponen K,
Savontaus ML,
Nikoskelainen E,
Zeviani M,
Carrara F,
Horvath R,
Karcagi V,
Spruijt L,
de Coo IF,
Smeets HJ,
Chinnery PF.
Mitochondrial Research Group, The Medical School, Framlington Place, Newcastle upon Tyne, NE2 4HH, United Kingdom.
Mitochondrial DNA (mtDNA) mutations are a major cause of human disease. A large number of different molecular defects ultimately compromise oxidative phosphorylation, but it is not clear why the same biochemical defect can cause diverse clinical phenotypes. There is emerging evidence that nuclear genes modulate the phenotype of primary mtDNA disorders. Here, we define an X-chromosomal haplotype that interacts with specific MTND mutations to cause visual failure in the most common mtDNA disease, Leber hereditary optic neuropathy. This effect is independent of the mtDNA genetic background and explains the variable penetrance and sex bias that characterizes this disorder.
PMID: 16380918 [PubMed - indexed for MEDLINE]
PMCID: PMC1285165