The impact of non-neutral synonymous mutations when inferring selection on non-synonymous mutations.

IF 5.1 3区 生物学 Q2 GENETICS & HEREDITY
Genetics Pub Date : 2025-09-27 DOI:10.1093/genetics/iyaf200
Aina Martinez I Zurita, Christopher C Kyriazis, Kirk E Lohmueller
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Abstract

The distribution of fitness effects (DFE) describes the proportions of new mutations that have different effects on fitness. Accurate measurements of the DFE are important because the DFE is a fundamental parameter in evolutionary genetics and has implications for our understanding of other phenomena like complex disease or inbreeding depression. Current computational methods to infer the DFE for non-synonymous mutations from natural variation first estimate demographic parameters from synonymous variants to control for the effects of demography and background selection. Then, conditional on these parameters, the DFE is then inferred for non-synonymous mutations. This approach relies on the assumption that synonymous variants are neutrally evolving. However, some evidence points toward synonymous mutations having measurable effects on fitness. To test whether selection on synonymous mutations affects inference of the DFE of non-synonymous mutations, we simulated several possible models of selection on synonymous mutations using SLiM and attempted to recover the DFE of non-synonymous mutations using Fit∂a∂i, a common method for DFE inference. Our results show that the presence of selection on synonymous variants leads to incorrect inferences of recent population growth. Furthermore, under certain parameter combinations with pervasive selection on synonymous mutations, the inferred DFEs for non-synonymous mutations show an inflated proportion of highly deleterious and nearly-neutral mutations. However, this bias can be eliminated if the correct demographic parameters are used for DFE inference instead of the biased ones inferred from synonymous variants. Our work demonstrates how unmodeled selection on synonymous mutations may affect downstream inferences of the DFE.

非中性同义突变对非同义突变选择的影响。
适应度效应分布(DFE)描述了对适应度有不同影响的新突变的比例。DFE的精确测量很重要,因为DFE是进化遗传学的一个基本参数,对我们理解复杂疾病或近亲繁殖抑郁症等其他现象具有重要意义。目前从自然变异中推断非同义突变DFE的计算方法首先从同义变异中估计人口统计学参数,以控制人口统计学和背景选择的影响。然后,以这些参数为条件,推断非同义突变的DFE。这种方法依赖于同义变体中性演化的假设。然而,一些证据表明,同义突变对适应性有可测量的影响。为了测试同义突变的选择是否会影响非同义突变的DFE推断,我们使用SLiM模拟了几种可能的同义突变选择模型,并尝试使用常见的DFE推断方法Fit∂a∂i来恢复非同义突变的DFE。我们的研究结果表明,同义变异的选择导致了对近期人口增长的不正确推断。此外,在对同义突变进行普遍选择的某些参数组合下,推断出的非同义突变的dfe显示出高度有害和接近中性突变的比例过高。然而,如果将正确的人口统计参数用于DFE推断,而不是从同义变体推断出的有偏见的参数,则可以消除这种偏差。我们的工作证明了对同义突变的未建模选择如何影响DFE的下游推论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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