Department of Biological Statistics and Computational Biology, Cornell University, Ithaca, New York 14853.
Department of Molecular Biology and Genetics, Cornell University, Ithaca, New York 14853.
Genetics. 2019 Mar;211(3):1005-1017. doi: 10.1534/genetics.118.301893. Epub 2019 Jan 24.
Estimating fitness differences between allelic variants is a central goal of experimental evolution. Current methods for inferring such differences from allele frequency time series typically assume that the effects of selection can be described by a fixed selection coefficient. However, fitness is an aggregate of several components including mating success, fecundity, and viability. Distinguishing between these components could be critical in many scenarios. Here, we develop a flexible maximum likelihood framework that can disentangle different components of fitness from genotype frequency data, and estimate them individually in males and females. As a proof-of-principle, we apply our method to experimentally evolved cage populations of , in which we tracked the relative frequencies of a loss-of-function and wild-type allele of This X-linked gene produces a recessive yellow phenotype when disrupted and is involved in male courtship ability. We find that the fitness costs of the yellow phenotype take the form of substantially reduced mating preference of wild-type females for yellow males, together with a modest reduction in the viability of yellow males and females. Our framework should be generally applicable to situations where it is important to quantify fitness components of specific genetic variants, including quantitative characterization of the population dynamics of CRISPR gene drives.
估计等位变异之间的适应度差异是实验进化的核心目标。目前,从等位基因频率时间序列推断这些差异的方法通常假设选择的影响可以用固定的选择系数来描述。然而,适应度是几个组成部分的总和,包括交配成功率、繁殖力和存活率。在许多情况下,区分这些组成部分可能至关重要。在这里,我们开发了一个灵活的最大似然框架,可以从基因型频率数据中分离出适应度的不同组成部分,并分别在雄性和雌性中对它们进行估计。作为原理验证,我们将我们的方法应用于 的实验进化笼养种群,在这些种群中,我们追踪了一个功能丧失和野生型等位基因的相对频率。这个 X 连锁基因的破坏会产生隐性黄色表型,并且参与雄性求偶能力。我们发现,黄色表型的适应度代价表现为野生型雌性对黄色雄性的交配偏好大大降低,以及黄色雄性和雌性的存活率略有降低。我们的框架应该普遍适用于需要量化特定遗传变异的适应度组成部分的情况,包括对 CRISPR 基因驱动的种群动态进行定量描述。