Department of Ecology and Evolutionary Biology, University of California, Irvine, CA 92697-2525, USA.
Mol Ecol. 2012 Oct;21(20):4913-6. doi: 10.1111/j.1365-294x.2012.05745.x.
Combining experimental evolution with whole-genome resequencing is a promising new strategy for investigating the dynamics of evolutionary change. Published studies that have resequenced laboratory-selected populations of sexual organisms have typically focused on populations sampled at the end of an evolution experiment. These studies have attempted to associate particular alleles with phenotypic change and attempted to distinguish between different theoretical models of adaptation. However, neither the population used to initiate the experiment nor multiple time points sampled during the evolutionary trajectory are generally available for examination. In this issue of Molecular Ecology, Orozco-terWengel et al. (2012) take a significant step forward by estimating genome-wide allele frequencies at the start, 15 generations into and at the end of a 37-generation Drosophila experimental evolution study. The authors identify regions of the genome that have responded to laboratory selection and describe the temporal dynamics of allele frequency change. They identify two common trajectories for putatively adaptive alleles: alleles either gradually increase in frequency throughout the entire 37 generations or alleles plateau at a new frequency by generation 15. The identification of complex trajectories of alleles under selection contributes to a growing body of literature suggesting that simple models of adaptation, whereby beneficial alleles arise and increase in frequency unimpeded until they become fixed, may not adequately describe short-term response to selection.
将实验进化与全基因组重测序相结合,是研究进化变化动态的一种很有前途的新策略。已发表的对性生物的实验室选择种群进行重测序的研究,通常侧重于在进化实验结束时对种群进行抽样。这些研究试图将特定的等位基因与表型变化联系起来,并试图区分不同的适应性理论模型。然而,通常无法检查用于启动实验的种群,也无法检查进化轨迹中的多个时间点。在本期《分子生态学》中,Orozco-terWengel 等人(2012)向前迈出了重要的一步,他们估计了 37 代果蝇实验进化研究开始时、15 代时和结束时的全基因组等位基因频率。作者确定了对实验室选择有反应的基因组区域,并描述了等位基因频率变化的时间动态。他们确定了两个假定适应性等位基因的常见轨迹:等位基因要么在整个 37 代中逐渐增加频率,要么在第 15 代时在新频率上达到稳定。选择下的等位基因的复杂轨迹的识别有助于越来越多的文献表明,适应性的简单模型,即有利的等位基因不受阻碍地出现并增加频率,直到它们固定下来,可能无法充分描述对选择的短期反应。