博物馆基因组学揭示拟南芥的时间遗传停滞和全球遗传多样性。

IF 3.9 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Lua Lopez, Patricia L M Lang, Stephanie Marciniak, Logan Kistler, Sergio M Latorre, Asnake Haile, Eleanna Vasquez Cerda, Diana Gamba, Yuxing Xu, Patrick Woods, Mistire Yifru, Jeffrey Kerby, John K McKay, Christopher G Oakley, Jon Ågren, Tigist Wondimu, Collins Bulafu, George H Perry, Hernán A Burbano, Jesse R Lasky
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引用次数: 0

摘要

随着时间的推移,种群遗传变异的全球模式为保持多样性的进化过程提供了一个窗口。随着时间的推移,谱系可能扩大或缩小其分布,导致群体遗传组成的更替。在单个基因座上,迁移、漂移和选择(以及其他过程)可能影响等位基因频率。博物馆中分布广泛的物种标本为了解未被充分研究的种群及其随时间变化的遗传学提供了一个独特的窗口。在这里,我们对130个植物标本馆标本和91个新的拟南芥野外标本进行了基因组测序,并将这些基因组与已发表的基因组相结合。我们寻求更广泛的物种基因组多样性视角,并测试种群基因组组成是否随时间而变化。我们在非洲的一系列人口中记录了广泛的和以前未被描述的多样性,这些人口受到人为气候变化的威胁。随着时间的推移,我们没有发现种群的基因组组成发生了巨大变化。相反,我们发现,在比较相隔185公里的欧亚种群时,每100年的遗传变化模式与此相同,这可能是由于漂变和不断变化的选择的结合。在物候和生理QTL上,我们只发现了混合的多基因适应信号。我们确实发现,在不同的个体中保守的基因显示出定向等位基因频率变化水平的改变,这可能是由于不同的净化和背景选择。我们的研究强调了博物馆标本如何揭示种群多样性的新维度,并展示了野生种群在最近的历史中是如何进化的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Museum Genomics Reveals Temporal Genetic Stasis and Global Genetic Diversity in Arabidopsis thaliana.

Global patterns of population genetic variation through time offer a window into evolutionary processes that maintain diversity. Over time, lineages may expand or contract their distribution, causing turnover in population genetic composition. At individual loci, migration, drift and selection (among other processes) may affect allele frequencies. Museum specimens of widely distributed species offer a unique window into the genetics of understudied populations and changes over time. Here, we sequenced genomes of 130 herbarium specimens and 91 new field collections of Arabidopsis thaliana and combined these with published genomes. We sought a broader view of genomic diversity across the species and to test if population genomic composition is changing through time. We documented extensive and previously uncharacterised diversity in a range of populations in Africa, populations that are under threat from anthropogenic climate change. Through time, we did not find dramatic changes in genomic composition of populations. Instead, we found a pattern of genetic change every 100 years of the same magnitude seen when comparing Eurasian populations that are 185 km apart, potentially due to a combination of drift and changing selection. We found only mixed signals of polygenic adaptation at phenology and physiology QTL. We did find that genes conserved across eudicots show altered levels of directional allele frequency change, potentially due to variable purifying and background selection. Our study highlights how museum specimens can reveal new dimensions of population diversity and show how wild populations are evolving in recent history.

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来源期刊
Molecular Ecology
Molecular Ecology 生物-进化生物学
CiteScore
8.40
自引率
10.20%
发文量
472
审稿时长
1 months
期刊介绍: Molecular Ecology publishes papers that utilize molecular genetic techniques to address consequential questions in ecology, evolution, behaviour and conservation. Studies may employ neutral markers for inference about ecological and evolutionary processes or examine ecologically important genes and their products directly. We discourage papers that are primarily descriptive and are relevant only to the taxon being studied. Papers reporting on molecular marker development, molecular diagnostics, barcoding, or DNA taxonomy, or technical methods should be re-directed to our sister journal, Molecular Ecology Resources. Likewise, papers with a strongly applied focus should be submitted to Evolutionary Applications. Research areas of interest to Molecular Ecology include: * population structure and phylogeography * reproductive strategies * relatedness and kin selection * sex allocation * population genetic theory * analytical methods development * conservation genetics * speciation genetics * microbial biodiversity * evolutionary dynamics of QTLs * ecological interactions * molecular adaptation and environmental genomics * impact of genetically modified organisms
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