Piganeau G, Eyre-Walker A
Center for the Study of Evolution, School of Biological Sciences, Biols, Sussex University, BN1 9QG Brighton, UK.
Heredity (Edinb). 2004 Apr;92(4):282-8. doi: 10.1038/sj.hdy.6800413.
In an attempt to resolve the controversy about whether recombination occurs in human mtDNA, we have analysed three recently published data sets of complete mtDNA sequences along with 10 RFLP data sets. We have analysed the relationship between linkage disequilibrium (LD) and distance between sites under a variety of conditions using two measures of LD, r2 and /D'/. We find that there is a negative correlation between r2 and distance in the majority of data sets, but no overall trend for /D'/. Five out of six mtDNA sequence data sets show an excess of homoplasy, but this could be due to either recombination or hypervariable sites. Two additional recombination detection methods used, Geneconv and Maximum Chi-Square, showed nonsignificant results. The overall significance of these findings is hard to quantify because of nonindependence, but our results suggest a lack of evidence for recombination in human mtDNA.
为了解决关于人类线粒体DNA(mtDNA)是否发生重组的争议,我们分析了最近发表的三个完整mtDNA序列数据集以及10个限制性片段长度多态性(RFLP)数据集。我们使用两种连锁不平衡(LD)度量方法,即r2和/D'/,分析了在各种条件下LD与位点间距离之间的关系。我们发现,在大多数数据集中,r2与距离呈负相关,但/D'/没有总体趋势。六个mtDNA序列数据集中有五个显示出过多的同塑性,但这可能是由于重组或高变位点所致。所使用的另外两种重组检测方法,即基因转换(Geneconv)和最大卡方检验,结果不显著。由于数据非独立性,这些发现的总体显著性难以量化,但我们的结果表明缺乏人类mtDNA发生重组的证据。