Abstract
A T→G transversion at nt 8993 in mitochondrial DNA of MTATP6 (encoding ATPase 6 of complex V of the respiratory chain) causes impaired mitochondrial ATP synthesis in two related mitochondrial disorders: neuropathy, ataxia and retinitis pigmentosa1 and maternally inherited Leigh syndrome2. To overcome the biochemical defect, we expressed wildtype ATPase 6 protein allotopically3 from nucleus-transfected constructs encoding an amino-terminal mitochondrial targeting signal appended to a recoded ATPase 6 gene (made compatible with the universal genetic code) that also contained a carboxy-terminal FLAG epitope tag. After transfection of human cells, the precursor polypeptide was expressed, imported into and processed within mitochondria, and incorporated into complex V. Allotopic expression of stably transfected constructs in cytoplasmic hybrids (cybrids) homoplasmic with respect to the 8993T→G mutation showed a significantly improved recovery after growth in selective medium as well as a significant increase in ATP synthesis. This is the first successful demonstration of allotopic expression of an mtDNA-encoded polypeptide in mammalian cells and could form the basis of a genetic approach to treat a number of human mitochondrial disorders.
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Acknowledgements
We thank S. Goff and E. Bacharach for advice and H. Du for technical assistance. This work was supported by grants from the US National Institutes of Health (to G.M., E.A.S. and J.G.) and the Muscular Dystrophy Association (to E.A.S. and G.M.).
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Manfredi, G., Fu, J., Ojaimi, J. et al. Rescue of a deficiency in ATP synthesis by transfer of MTATP6, a mitochondrial DNA-encoded gene, to the nucleus. Nat Genet 30, 394–399 (2002). https://doi.org/10.1038/ng851
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DOI: https://doi.org/10.1038/ng851
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