Henn Brenna M, Gignoux Christopher R, Feldman Marcus W, Mountain Joanna L
Department of Anthropology, Stanford University, USA.
Mol Biol Evol. 2009 Jan;26(1):217-30. doi: 10.1093/molbev/msn244. Epub 2008 Nov 4.
Previous research has established a discrepancy of nearly an order of magnitude between pedigree-based and phylogeny-based (human vs. chimpanzee) estimates of the mitochondrial DNA (mtDNA) control region mutation rate. We characterize the time dependency of the human mitochondrial hypervariable region one mutation rate by generating 14 new phylogeny-based mutation rate estimates using within-human comparisons and archaeological dates. Rate estimates based on population events between 15,000 and 50,000 years ago are at least 2-fold lower than pedigree-based estimates. These within-human estimates are also higher than estimates generated from phylogeny-based human-chimpanzee comparisons. Our new estimates establish a rapid decay in evolutionary mutation rate between approximately 2,500 and 50,000 years ago and a slow decay from 50,000 to 6 Ma. We then extend this analysis to the mtDNA-coding region. Our within-human coding region mutation rate estimates display a similar, though less rapid, time-dependent decay. We explore the possibility that multiple hits explain the discrepancy between pedigree-based and phylogeny-based mutation rates. We conclude that whereas nucleotide substitution models incorporating multiple hits do provide a possible explanation for the discrepancy between pedigree-based and human-chimpanzee mutation rate estimates, they do not explain the rapid decline of within-human rate estimates. We propose that demographic processes such as serial bottlenecks prior to the Holocene could explain the difference between rates estimated before and after 15,000 years ago. Our findings suggest that human mtDNA estimates of dates of population and phylogenetic events should be adjusted in light of this time dependency of the mutation rate estimates.
先前的研究表明,基于谱系和基于系统发育(人类与黑猩猩)的线粒体DNA(mtDNA)控制区突变率估计值之间存在近一个数量级的差异。我们通过利用人类内部比较和考古年代生成14个新的基于系统发育的突变率估计值,来描述人类线粒体高变区I突变率的时间依赖性。基于15000至50000年前种群事件的突变率估计值至少比基于谱系的估计值低2倍。这些人类内部的估计值也高于基于人类与黑猩猩系统发育比较得出的估计值。我们的新估计值表明,在大约2500至50000年前,进化突变率迅速下降,而从50000年前到600万年前则缓慢下降。然后,我们将此分析扩展到mtDNA编码区。我们对人类编码区突变率的估计值显示出类似的、虽不那么迅速的时间依赖性下降。我们探讨了多次击中解释基于谱系和基于系统发育的突变率之间差异的可能性。我们得出结论,虽然纳入多次击中的核苷酸替代模型确实为基于谱系和人类与黑猩猩突变率估计值之间的差异提供了一种可能的解释,但它们并不能解释人类内部突变率估计值的迅速下降。我们提出,诸如全新世之前的连续瓶颈等人口统计学过程可以解释15000年前前后估计率之间的差异。我们的研究结果表明,鉴于突变率估计值的这种时间依赖性,人类mtDNA对种群和系统发育事件日期的估计应进行调整。