Resolving the source of branch length variation in the Y chromosome phylogeny

IF 10.1 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Genome Biology Pub Date : 2025-01-06 DOI:10.1186/s13059-024-03468-4
Yaniv Swiel, Janet Kelso, Stéphane Peyrégne
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Abstract

Genetic variation in the non-recombining part of the human Y chromosome has provided important insight into the paternal history of human populations. However, a significant and yet unexplained branch length variation of Y chromosome lineages has been observed, notably amongst those that are highly diverged from the human reference Y chromosome. Understanding the origin of this variation, which has previously been attributed to changes in generation time, mutation rate, or efficacy of selection, is important for accurately reconstructing human evolutionary and demographic history. Here, we analyze Y chromosomes from present-day and ancient modern humans, as well as Neandertals, and show that branch length variation amongst human Y chromosomes cannot solely be explained by differences in demographic or biological processes. Instead, reference bias results in mutations being missed on Y chromosomes that are highly diverged from the reference used for alignment. We show that masking fast-evolving, highly divergent regions of the human Y chromosome mitigates the effect of this bias and enables more accurate determination of branch lengths in the Y chromosome phylogeny. We show that our approach allows us to estimate the age of ancient samples from Y chromosome sequence data and provide updated estimates for the time to the most recent common ancestor using the portion of the Y chromosome where the effect of reference bias is minimized.
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解决Y染色体系统发育中分支长度变异的来源
人类Y染色体非重组部分的遗传变异为人类种群的父系历史提供了重要的见解。然而,已经观察到Y染色体谱系中一个重要的但尚未解释的分支长度变化,特别是那些与人类参考Y染色体高度分化的分支长度变化。这种变异以前被认为是世代时间、突变率或选择效力的变化,了解其起源对于准确重建人类进化和人口统计学历史非常重要。在这里,我们分析了来自现代和古代现代人以及尼安德特人的Y染色体,并表明人类Y染色体分支长度的变化不能仅仅用人口统计学或生物学过程的差异来解释。相反,参考偏差导致与用于比对的参考高度偏离的Y染色体上的突变被遗漏。我们发现,掩盖人类Y染色体快速进化、高度分化的区域减轻了这种偏见的影响,并使Y染色体系统发育中分支长度的测定更加准确。我们表明,我们的方法允许我们从Y染色体序列数据中估计古代样本的年龄,并使用参考偏差影响最小的Y染色体部分提供最新的共同祖先时间估计。
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来源期刊
Genome Biology
Genome Biology Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
21.00
自引率
3.30%
发文量
241
审稿时长
2 months
期刊介绍: Genome Biology stands as a premier platform for exceptional research across all domains of biology and biomedicine, explored through a genomic and post-genomic lens. With an impressive impact factor of 12.3 (2022),* the journal secures its position as the 3rd-ranked research journal in the Genetics and Heredity category and the 2nd-ranked research journal in the Biotechnology and Applied Microbiology category by Thomson Reuters. Notably, Genome Biology holds the distinction of being the highest-ranked open-access journal in this category. Our dedicated team of highly trained in-house Editors collaborates closely with our esteemed Editorial Board of international experts, ensuring the journal remains on the forefront of scientific advances and community standards. Regular engagement with researchers at conferences and institute visits underscores our commitment to staying abreast of the latest developments in the field.
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