Institute of Evolutionary Biology, and Centre for Infection Immunity and Evolution, University of Edinburgh, Edinburgh, United Kingdom.
Mol Biol Evol. 2012 Nov;29(11):3459-73. doi: 10.1093/molbev/mss150. Epub 2012 Jun 7.
An absolute timescale for evolution is essential if we are to associate evolutionary phenomena, such as adaptation or speciation, with potential causes, such as geological activity or climatic change. Timescales in most phylogenetic studies use geologically dated fossils or phylogeographic events as calibration points, but more recently, it has also become possible to use experimentally derived estimates of the mutation rate as a proxy for substitution rates. The large radiation of drosophilid taxa endemic to the Hawaiian islands has provided multiple calibration points for the Drosophila phylogeny, thanks to the "conveyor belt" process by which this archipelago forms and is colonized by species. However, published date estimates for key nodes in the Drosophila phylogeny vary widely, and many are based on simplistic models of colonization and coalescence or on estimates of island age that are not current. In this study, we use new sequence data from seven species of Hawaiian Drosophila to examine a range of explicit coalescent models and estimate substitution rates. We use these rates, along with a published experimentally determined mutation rate, to date key events in drosophilid evolution. Surprisingly, our estimate for the date for the most recent common ancestor of the genus Drosophila based on mutation rate (25-40 Ma) is closer to being compatible with independent fossil-derived dates (20-50 Ma) than are most of the Hawaiian-calibration models and also has smaller uncertainty. We find that Hawaiian-calibrated dates are extremely sensitive to model choice and give rise to point estimates that range between 26 and 192 Ma, depending on the details of the model. Potential problems with the Hawaiian calibration may arise from systematic variation in the molecular clock due to the long generation time of Hawaiian Drosophila compared with other Drosophila and/or uncertainty in linking island formation dates with colonization dates. As either source of error will bias estimates of divergence time, we suggest mutation rate estimates be used until better models are available.
如果我们要将进化现象(如适应或物种形成)与潜在原因(如地质活动或气候变化)联系起来,那么进化的绝对时间尺度是必不可少的。大多数系统发育研究中的时间尺度都使用地质年代化石或系统地理学事件作为校准点,但最近,使用实验得出的突变率估计值作为替代率的替代方法也变得可行。由于这个群岛形成和被物种殖民的“输送带”过程,夏威夷特有的果蝇分类群的大量辐射为果蝇系统发育提供了多个校准点。然而,发表的果蝇系统发育关键节点的日期估计值差异很大,其中许多是基于简单的殖民和融合模型,或者基于的岛屿年龄估计值并不准确。在这项研究中,我们使用来自七种夏威夷果蝇的新序列数据来检验一系列明确的合并模型并估计替代率。我们使用这些速率以及已发表的实验确定的突变率来确定果蝇进化中的关键事件的日期。令人惊讶的是,我们基于突变率(25-40 Ma)对果蝇属最近共同祖先日期的估计(25-40 Ma)与独立的化石衍生日期(20-50 Ma)更接近,而不是大多数夏威夷校准模型,并且不确定性也更小。我们发现,夏威夷校准的日期对模型选择非常敏感,并且取决于模型的详细信息,会产生 26 到 192 Ma 之间的点估计值。由于与其他果蝇相比,夏威夷果蝇的世代时间较长,以及将岛屿形成日期与殖民日期联系起来的不确定性,可能会导致分子钟的系统变化,从而出现与夏威夷校准相关的潜在问题。由于这两种误差源都会偏置分歧时间的估计值,因此我们建议在有更好的模型可用之前使用突变率估计值。