Heteroplasmy of Mouse mtDNA Is Genetically Unstable and Results in Altered Behavior and Cognition
Author(s) -
Mark S. Sharpley,
Christine Marciniak,
Kristin EckelMahan,
Meagan J. McManus,
Marco Crimi,
Katrina G. Waymire,
Chun Shi Lin,
Satoru Masubuchi,
Nicole Friend,
Maya A. Koike,
Dimitra Chalkia,
Grant R. MacGregor,
Paolo Sassone–Corsi,
Douglas C. Wallace
Publication year - 2012
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2012.09.004
Subject(s) - heteroplasmy , biology , genetics , mitochondrial dna , non mendelian inheritance , congenic , phenotype , inheritance (genetic algorithm) , introgression , gene
Maternal inheritance of mtDNA is the rule in most animals, but the reasons for this pattern remain unclear. To investigate the consequence of overriding uniparental inheritance, we generated mice containing an admixture (heteroplasmy) of NZB and 129S6 mtDNAs in the presence of a congenic C57BL/6J nuclear background. Analysis of the segregation of the two mtDNAs across subsequent maternal generations revealed that proportion of NZB mtDNA was preferentially reduced. Ultimately, this segregation process produced NZB-129 heteroplasmic mice and their NZB or 129 mtDNA homoplasmic counterparts. Phenotypic comparison of these three mtDNA lines demonstrated that the NZB-129 heteroplasmic mice, but neither homoplasmic counterpart, had reduced activity, food intake, respiratory exchange ratio; accentuated stress response; and cognitive impairment. Therefore, admixture of two normal but different mouse mtDNAs can be genetically unstable and can produce adverse physiological effects, factors that may explain the advantage of uniparental inheritance of mtDNA.
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