{"title":"Enrichment of hard sweeps on the X chromosome compared to autosomes in six Drosophila species.","authors":"Mariana Harris, Bernard Kim, Nandita Garud","doi":"10.1101/2023.06.21.545888","DOIUrl":null,"url":null,"abstract":"<p><p>The X chromosome, being hemizygous in males, is exposed one third of the time increasing the visibility of new mutations to natural selection, potentially leading to different evolutionary dynamics than autosomes. Recently, we found an enrichment of hard selective sweeps over soft selective sweeps on the X chromosome relative to the autosomes in a North American population of <i>Drosophila melanogaster</i>. To understand whether this enrichment is a universal feature of evolution on the X chromosome, we analyze diversity patterns across six commonly studied <i>Drosophila</i> species. We find an increased proportion of regions with steep reductions in diversity and elevated homozygosity on the X chromosome compared to autosomes. To assess if these signatures are consistent with positive selection, we simulate a wide variety of evolutionary scenarios spanning variations in demography, mutation rate, recombination rate, background selection, hard sweeps, and soft sweeps, and find that the diversity patterns observed on the X are most consistent with hard sweeps. Our findings highlight the importance of sex chromosomes in driving evolutionary processes and suggest that hard sweeps have played a significant role in shaping diversity patterns on the X chromosome across multiple <i>Drosophila</i> species.</p>","PeriodicalId":9343,"journal":{"name":"Brittonia","volume":"62 1","pages":""},"PeriodicalIF":0.6000,"publicationDate":"2023-12-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10723260/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Brittonia","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1101/2023.06.21.545888","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
The X chromosome, being hemizygous in males, is exposed one third of the time increasing the visibility of new mutations to natural selection, potentially leading to different evolutionary dynamics than autosomes. Recently, we found an enrichment of hard selective sweeps over soft selective sweeps on the X chromosome relative to the autosomes in a North American population of Drosophila melanogaster. To understand whether this enrichment is a universal feature of evolution on the X chromosome, we analyze diversity patterns across six commonly studied Drosophila species. We find an increased proportion of regions with steep reductions in diversity and elevated homozygosity on the X chromosome compared to autosomes. To assess if these signatures are consistent with positive selection, we simulate a wide variety of evolutionary scenarios spanning variations in demography, mutation rate, recombination rate, background selection, hard sweeps, and soft sweeps, and find that the diversity patterns observed on the X are most consistent with hard sweeps. Our findings highlight the importance of sex chromosomes in driving evolutionary processes and suggest that hard sweeps have played a significant role in shaping diversity patterns on the X chromosome across multiple Drosophila species.
X 染色体是雄性的半杂合子,有三分之一的时间暴露在自然选择面前,增加了新突变的能见度,可能导致与常染色体不同的进化动态。最近,我们在北美的一个黑腹果蝇种群中发现,相对于常染色体,X 染色体上的硬选择性扫描比软选择性扫描更丰富。为了了解这种富集是否是 X 染色体进化的普遍特征,我们分析了 6 个常用果蝇物种的多样性模式。我们发现,与常染色体相比,X 染色体上多样性急剧下降和同源性升高的区域比例有所增加。为了评估这些特征是否与正向选择一致,我们模拟了多种进化情景,包括人口统计、突变率、重组率、背景选择、硬横扫和软横扫等方面的变化,结果发现在 X 染色体上观察到的多样性模式与硬横扫最为一致。我们的发现凸显了性染色体在推动进化过程中的重要性,并表明在多个果蝇物种中,硬横扫在塑造 X 染色体多样性模式方面发挥了重要作用。
期刊介绍:
Since 1931, Brittonia, assuming the broadest possible definition of the field of systematic botany, has been an important outlet for the publication of original research articles on anatomy, botanical history, chemotaxonomy, morphology, paleobotany, phylogenetic systematics, taxonomy, and phytogeography. Each issue contains articles by the staff of The New York Botanical Garden and outside contributors, book reviews, and announcements.