大反转影响鹌鹑的多样化和基因组进化。

IF 4.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Sara Ravagni, Santiago Montero-Mendieta, Jennifer A. Leonard, Matthew T. Webster, Matthew J. Christmas, Ignas Bunikis, José Domingo Rodríguez-Teijeiro, Ines Sanchez-Donoso, Carles Vilà
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引用次数: 0

摘要

染色体倒位,通过抑制重组,可以深刻地塑造基因组进化和驱动适应。普通鹌鹑(Coturnix Coturnix)是一种具有广泛古北繁殖范围的高流动性鸟类,我们之前在1号染色体上发现了与不同表型和限制地理分布相关的大量倒置。在这里,使用新的从头开始的基因组组装,我们描述了这种倒置,并揭示了在物种范围内分离的2号染色体上额外的古老结构变异:要么是两个推定相关的倒置,要么是由于脚手架限制而出现的单个大倒置。总的来说,这些倒位占据了鹌鹑基因组的15.6% (153.6 Mbp),创造了高度分化的单倍型,这些单倍型在100多万年前就已经分化了。虽然1号染色体倒置与表型差异有关,包括形态和迁移行为,但2号染色体倒置没有这种关联。值得注意的是,所有反转区都表现出有效种群大小的减小和净化选择的放松,非同义对同义替代比(N/S)的升高证明了这一点。这表明逆转录,特别是1号染色体上受地理限制的逆转录,可能是多样化的动力,加速功能变异的积累,并可能有助于地方适应,特别是在孤立的岛屿人口中。我们的发现证明了大规模的染色体重排是如何划分基因组的,从而在一个单一的、高度移动的物种中培育出不同的进化轨迹。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Large Inversions Shape Diversification and Genome Evolution in Common Quails

Chromosomal inversions, by suppressing recombination, can profoundly shape genome evolution and drive adaptation. In the common quail (Coturnix coturnix), a highly mobile bird with a vast Palearctic breeding range, we previously identified a massive inversion on chromosome 1 associated with distinct phenotypes and restricted geographic distribution. Here, using a new de novo genome assembly, we characterise this inversion and uncover additional, ancient structural variation on chromosome 2 that segregates across the species' range: either two putatively linked inversions or a single, large inversion that appears as two due to scaffolding limitations. Together, the inversions encompass a remarkable 15.6% of the quail genome (153.6 Mbp), creating highly divergent haplotypes that diverged over a million years ago. While the chromosome 1 inversion is linked to phenotypic differences, including morphology and migratory behaviour, the chromosome 2 inversion(s) show no such association. Notably, all inversion regions exhibit reduced effective population size and a relaxation of purifying selection, evidenced by elevated nonsynonymous-to-synonymous substitution ratios (N/S). This suggests that inversions, particularly the geographically restricted one on chromosome 1, may act as engines of diversification, accelerating the accumulation of functional variation and potentially contributing to local adaptation, especially within isolated island populations. Our findings demonstrate how large-scale chromosomal rearrangements can compartmentalise a genome, fostering distinct evolutionary trajectories within a single, highly mobile species.

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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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