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Vol. 11, Issue 7, 2349-2358, July 2000


and
§
Departments of *Genetics and Development and
Large-scale rearrangements of mitochondrial DNA (mtDNA; i.e.,
partial duplications [dup-mtDNAs] and deletions
[
Neurology, Columbia University, New York, New York
10032
-mtDNAs]) coexist in tissues in a subset of patients with
sporadic mitochondrial disorders. In order to study the dynamic
relationship among rearranged and wild-type mtDNA (wt-mtDNA) species,
we created transmitochondrial cell lines harboring various proportions
of wt-,
-, and dup-mtDNAs from two patients. After prolonged culture
in nonselective media, cells that contained initially 100% dup-mtDNAs
became heteroplasmic, containing both wild-type and rearranged mtDNAs,
likely generated via intramolecular recombination events. However, in
cells that contained initially a mixture of both wt- and
-mtDNAs, we
did not observe any dup-mtDNAs or other new forms of rearranged mtDNAs, perhaps because the two species were physically separated and were
therefore unable to recombine. The ratio of wt-mtDNA to
-mtDNAs remained stable in all cells examined, suggesting that there was no
replicative advantage for the smaller deleted molecules. Finally, in
cells containing a mixture of monomeric and dimeric forms of a specific
-mtDNA, we found that the mtDNA population shifted towards
homoplasmic dimers, suggesting that there may be circumstances under
which the cells favor molecules with multiple replication origins,
independent of the size of the molecule.
Present address: Department of Neurology and
Neuroscience, Weill Medical College of Cornell University, 1300 York
Avenue, New York, NY 10021.
§
Corresponding author: Department of Neurology, Room
P&S 4-431, Columbia University, 630 West 168th Street, New York, NY
10032. E-mail address: eas3{at}columbia.edu.
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