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Vol. 13, Issue 11, 3836-3844, November 2002

and
§
Departments of *Neurology and Unlike most organisms, the mitochondrial DNA (mtDNA) of
Chlamydomonas reinhardtii, a green alga, does not encode
subunit 6 of F0F1-ATP synthase. We hypothesized
that C. reinhardtii ATPase 6 is nucleus encoded and
identified cDNAs and a single-copy nuclear gene specifying this subunit
(CrATP6, with eight exons, four of which encode a
mitochondrial targeting signal). Although the algal and human
ATP6 genes are in different subcellular compartments and
the encoded polypeptides are highly diverged, their secondary structures are remarkably similar. When CrATP6 was
expressed in human cells, a significant amount of the precursor
polypeptide was targeted to mitochondria, the mitochondrial targeting
signal was cleaved within the organelle, and the mature
polypeptide was assembled into human ATP synthase. In spite of the
evolutionary distance between algae and mammals, C.
reinhardtii ATPase 6 functioned in human cells, because
deficiencies in both cell viability and ATP synthesis in
transmitochondrial cell lines harboring a pathogenic mutation in the
human mtDNA-encoded ATP6 gene were overcome by expression of CrATP6. The ability to express a
nucleus-encoded version of a mammalian mtDNA-encoded protein may
provide a way to import other highly hydrophobic proteins into
mitochondria and could serve as the basis for a gene therapy approach
to treat human mitochondrial diseases.
Genetics and
Development, Columbia University College of Physicians and Surgeons,
New York, New York 10032; and
Department of Cell
Biology, University of Texas Southwestern Medical Center, Dallas, Texas
75390
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