Evolutionary genetics: direct evidence of recombination in human mitochondrial DNA.

Bibliographic Collection: 
APE
Publication Type: Journal Article
Authors: Ladoukakis, E D; Eyre-Walker, A
Year of Publication: 2004
Journal: Heredity (Edinb)
Volume: 93
Issue: 4
Pagination: 321
Date Published: 2004 Oct
Publication Language: eng
ISSN: 0018-067X
Keywords: DNA, Mitochondrial, Humans, Recombination, Genetic
Abstract:

[Commentary paper]

Over the last 5 years, there has been considerable debate as to whether there is recombination in human mitochondrial DNA (mtDNA) (for references, see Piganeau and Eyre-Walker, 2004). That debate appears to have finally come to an end with the publication of some direct evidence of recombination. Schwartz and Vissing (2002), 2 years ago, presented the case of a 28-year-old man who had both maternal and paternally derived mtDNA in his muscle tissue – in all his other tissues he had only maternally derived mtDNA. It was the first time that paternal leakage and, consequently, heteroplasmy was observed in human mtDNA. In a recent paper, Kraytsberg et al (2004) take this observation one step further, and claim to show that there has been recombination between the maternal and paternal mtDNA in this individual.

DOI: 10.1038/sj.hdy.6800572
Alternate Journal: Heredity (Edinb)
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