A path integral approach for allele frequency dynamics under polygenic selection.

IF 3.3 3区 生物学 Q2 GENETICS & HEREDITY Genetics Pub Date : 2024-11-12 DOI:10.1093/genetics/iyae182
Nathan W Anderson, Lloyd Kirk, Joshua G Schraiber, Aaron P Ragsdale
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Abstract

Many phenotypic traits have a polygenic genetic basis, making it challenging to learn their genetic architectures and predict individual phenotypes. One promising avenue to resolve the genetic basis of complex traits is through evolve-and-resequence experiments, in which laboratory populations are exposed to some selective pressure and trait-contributing loci are identified by extreme frequency changes over the course of the experiment. However, small laboratory populations will experience substantial random genetic drift, and it is difficult to determine whether selection played a role in a given allele frequency change. Predicting allele frequency changes under drift and selection, even for alleles contributing to simple, monogenic traits, has remained a challenging problem. Recently, there have been efforts to apply the path integral, a method borrowed from physics, to solve this problem. So far, this approach has been limited to genic selection, and is therefore inadequate to capture the complexity of quantitative, highly polygenic traits that are commonly studied. Here we extend one of these path integral methods, the perturbation approximation, to selection scenarios that are of interest to quantitative genetics. We derive analytic expressions for the transition probability (i.e., the probability that an allele will change in frequency from x to y in time t) of an allele contributing to a trait subject to stabilizing selection, as well as that of an allele contributing to a trait rapidly adapting to a new phenotypic optimum. We use these expressions to characterize the use of allele frequency change to test for selection, as well as explore optimal design choices for evolve-and-resequence experiments to uncover the genetic architecture of polygenic traits under selection.

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多基因选择下等位基因频率动态的路径积分法
许多表型性状都有多基因遗传基础,因此了解其遗传结构并预测个体表型具有挑战性。解决复杂性状遗传基础的一个有希望的途径是通过 "进化与序列 "实验,在实验中,实验室种群面临一定的选择性压力,通过实验过程中的极端频率变化来确定性状贡献位点。然而,小规模的实验室群体会经历大量的随机遗传漂移,因此很难确定选择是否在特定等位基因频率变化中起了作用。预测漂移和选择作用下等位基因频率的变化,即使是预测简单的单基因性状的等位基因频率变化,仍然是一个具有挑战性的问题。最近,人们开始应用路径积分(一种借用物理学的方法)来解决这个问题。迄今为止,这种方法仅限于基因选择,因此不足以捕捉通常研究的定量、高度多基因性状的复杂性。在这里,我们将这些路径积分方法之一--扰动近似--扩展到数量遗传学感兴趣的选择情景中。我们推导出了受稳定选择影响的等位基因性状的过渡概率(即等位基因的频率在 t 时间内从 x 变为 y 的概率)以及快速适应新表型最佳性状的等位基因性状的过渡概率的解析表达式。我们利用这些表达式来描述利用等位基因频率变化来测试选择的特点,并探索进化和序列实验的最佳设计选择,以揭示选择下多基因性状的遗传结构。
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来源期刊
Genetics
Genetics GENETICS & HEREDITY-
CiteScore
6.90
自引率
6.10%
发文量
177
审稿时长
1.5 months
期刊介绍: GENETICS is published by the Genetics Society of America, a scholarly society that seeks to deepen our understanding of the living world by advancing our understanding of genetics. Since 1916, GENETICS has published high-quality, original research presenting novel findings bearing on genetics and genomics. The journal publishes empirical studies of organisms ranging from microbes to humans, as well as theoretical work. While it has an illustrious history, GENETICS has changed along with the communities it serves: it is not your mentor''s journal. The editors make decisions quickly – in around 30 days – without sacrificing the excellence and scholarship for which the journal has long been known. GENETICS is a peer reviewed, peer-edited journal, with an international reach and increasing visibility and impact. All editorial decisions are made through collaboration of at least two editors who are practicing scientists. GENETICS is constantly innovating: expanded types of content include Reviews, Commentary (current issues of interest to geneticists), Perspectives (historical), Primers (to introduce primary literature into the classroom), Toolbox Reviews, plus YeastBook, FlyBook, and WormBook (coming spring 2016). For particularly time-sensitive results, we publish Communications. As part of our mission to serve our communities, we''ve published thematic collections, including Genomic Selection, Multiparental Populations, Mouse Collaborative Cross, and the Genetics of Sex.
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