Evidence for mitochondrial DNA recombination in a human population of island Melanesia

被引:112
作者
Hagelberg, E
Goldman, N
Lió, P
Whelan, S
Schiefenhövel, W
Clegg, JB
Bowden, DK
机构
[1] Univ Cambridge, Dept Genet, Cambridge CB2 3EH, England
[2] Max Planck Inst Behav Physiol, D-82346 Andechs, Germany
[3] Univ Oxford, John Radcliffe Hosp, Inst Mol Med, MRC,Mol Haematol Unit, Oxford OX3 9DS, England
[4] Monash Univ, Dept Anat, Clayton, Vic 3168, Australia
基金
英国惠康基金;
关键词
human evolution; Melanesia; mitochondrial DNA; Polynesia; population genetics; recombination;
D O I
10.1098/rspb.1999.0663
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Mitochondrial DNA (mtDNA) analysis has proved useful in studies of recent human evolution and the genetic affinities of human groups of different geographical regions. As part of an extensive survey of mtDNA diversity in present-day Pacific populations, we obtained sequence information of the hypervariable mtDNA control region of 452 individuals from various localities in the western Pacific. The mtDNA types fell into three major groups which reflect the settlement history of the area. Interestingly, we detected an extremely rare point mutation at high frequency in the small island of Nguna in the Melanesian archipelago of Vanuatu. Phylogenetic analysis of the mtDNA data indicated that the mutation was present in individuals of separate mtDNA lineages. We propose that the multiple occurrence of a rare mutation event in one isolated locality is highly improbable, and that recombination between different mtDNA types is a more likely explanation for our observation. If correct, this conclusion has important implications for the use of mtDNA in phylogenetic and evolutionary studies.
引用
收藏
页码:485 / 492
页数:8
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