Mutation ages and population origins inferred from genomes in structured populations.

IF 5.1 3区 生物学 Q2 GENETICS & HEREDITY
Genetics Pub Date : 2025-09-23 DOI:10.1093/genetics/iyaf204
Anna A Nagel, Bruce Rannala
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引用次数: 0

Abstract

Inferring the time of origin (age) of mutations is an old question in population genetics and inferring their population of origin has become of particular interest with the sequencing of the Neanderthal genome. However, existing methods to infer mutation ages and populations of origin do not explicitly consider population structure, migration rates, and divergence times, which may bias estimates, and it is unclear how to even apply single-population estimators to structured populations. We develop a method to jointly estimate the time and population of origin of a mutation (as well as the ancestral and derived states) in a structured population using population genomic data and examine its statistical performance using simulations. Results indicate that mutation age and population of origin can be quite uncertain, even with long sequences or many samples, but this uncertainty is accurately captured using credible intervals/sets. The ancestral nucleotide state is relatively easy to infer. We apply our method to whole genome data from the 1000 Genomes Project, analyzing seven SNP mutations from six genes associated with human skin pigmentation for populations from Great Britain, China, and Kenya. Our results partially support previous conclusions, with the putative ancestral alleles from the literature matching our inferences, while the mutation age estimates only overlap in some cases.

从结构群体的基因组推断突变年龄和群体起源。
推断突变的起源时间(年龄)是种群遗传学中的一个老问题,推断它们的起源群体已经成为尼安德特人基因组测序的特别感兴趣的问题。然而,现有的推断突变年龄和起源种群的方法并没有明确考虑种群结构、迁移率和分化时间,这可能会导致估计偏差,而且尚不清楚如何将单种群估计器应用于结构化种群。我们开发了一种方法,利用群体基因组数据联合估计一个突变的时间和起源群体(以及祖先和衍生状态)在一个结构化群体中,并使用模拟检查其统计性能。结果表明,突变年龄和种群起源可能相当不确定,即使是长序列或许多样本,但这种不确定性可以使用可信区间/集准确捕获。祖先的核苷酸状态相对容易推断。我们将我们的方法应用于来自1000基因组计划的全基因组数据,分析了来自英国、中国和肯尼亚人群中与人类皮肤色素沉着相关的6个基因的7个SNP突变。我们的结果部分支持先前的结论,从文献中推测的祖先等位基因与我们的推断相符,而突变年龄估计仅在某些情况下重叠。
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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