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整合基因组学和多元进化数量遗传学:以性选择约束为例。

Integrating genomics and multivariate evolutionary quantitative genetics: a case study of constraints on sexual selection in .

机构信息

School of Biological Sciences, The University of Queensland, Saint Lucia, Queensland 4072, Australia.

Research School of Biology, Australian National University, Australian Capital Territory 0200, Australia.

出版信息

Proc Biol Sci. 2021 Oct 13;288(1960):20211785. doi: 10.1098/rspb.2021.1785.

Abstract

In evolutionary quantitative genetics, the genetic variance-covariance matrix, , and the vector of directional selection gradients, , are key parameters for predicting multivariate selection responses and genetic constraints. Historically, investigations of and have not overlapped with those dissecting the genetic basis of quantitative traits. Thus, it remains unknown whether these parameters reflect pleiotropic effects at individual loci. Here, we integrate multivariate genome-wide association study (GWAS) with and estimation in a well-studied system of multivariate constraint: sexual selection on male cuticular hydrocarbons (CHCs) in . In a panel of wild-derived re-sequenced lines, we augment genome-based restricted maximum likelihood to estimate alongside multivariate single nucleotide polymorphism (SNP) effects, detecting 532 significant associations from 1 652 276 SNPs. Constraint was evident, with lying in a direction of with low evolvability. Interestingly, minor frequency alleles typically increased male CHC-attractiveness suggesting opposing natural selection on . SNP effects were significantly misaligned with the major eigenvector of , , but well aligned to the second and third eigenvectors and . We discuss potential factors leading to these varied results including multivariate stabilizing selection and mutational bias. Our framework may be useful as researchers increasingly access genomic methods to study multivariate selection responses in wild populations.

摘要

在进化数量遗传学中,遗传方差-协方差矩阵 和方向选择梯度向量 是预测多元选择反应和遗传约束的关键参数。历史上,对 和 的研究并未与剖析数量性状遗传基础的研究重叠。因此,这些参数是否反映了单个基因座的多效性效应尚不清楚。在这里,我们将多维全基因组关联研究 (GWAS) 与 和 估计整合到一个经过充分研究的多维约束系统中: 对雄性表皮碳氢化合物 (CHC) 的性选择。在一组野生衍生的重测序品系中,我们通过基于基因组的受限最大似然法来估计 ,并检测到 1 652 276 个 SNP 中的 532 个显著关联。约束是明显的, 朝着低进化能力的 方向。有趣的是,低频等位基因通常会增加雄性 CHC 的吸引力,这表明 受到了相反的自然选择。SNP 效应与 的主要特征向量显著不一致,但与第二和第三个特征向量 和 一致。我们讨论了导致这些不同结果的潜在因素,包括多变量稳定选择和突变偏差。随着研究人员越来越多地利用基因组方法来研究野生种群中的多元选择反应,我们的框架可能会很有用。

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