{"title":"遗传漂变推动了鲑虱 Lepeophtheirus salmonis 的快速进化。","authors":"Andrew J Mongue, Robert B Baird","doi":"10.1093/evolut/qpae090","DOIUrl":null,"url":null,"abstract":"<p><p>How sex chromosomes evolve compared to autosomes remains an unresolved question in population genetics. Most studies focus on only a handful of taxa, resulting in uncertainty over whether observed patterns reflect general processes or idiosyncrasies in particular clades. For example, in female heterogametic (ZW) systems, bird Z chromosomes tend to evolve quickly but not adaptively, while in Lepidopterans they evolve adaptively, but not always quickly. To understand how these observations fit into broader evolutionary patterns, we explore Z chromosome evolution outside of these two well-studied clades. We utilize a publicly available genome, gene expression, population, and outgroup data in the salmon louse Lepeophtheirus salmonis, an important agricultural pest copepod. We find that the Z chromosome is faster evolving than autosomes, but that this effect is driven by increased drift rather than adaptive evolution. Due to high rates of female reproductive failure, the Z chromosome exhibits a slightly lower effective population size than the autosomes which is nonetheless to decrease efficiency of hemizygous selection acting on the Z. These results highlight the usefulness of organismal life history in calibrating population genetic expectations and demonstrate the value of the ever-expanding wealth of publicly available data to help resolve outstanding evolutionary questions.</p>","PeriodicalId":12082,"journal":{"name":"Evolution","volume":" ","pages":"1594-1605"},"PeriodicalIF":3.1000,"publicationDate":"2024-09-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Genetic drift drives faster-Z evolution in the salmon louse Lepeophtheirus salmonis.\",\"authors\":\"Andrew J Mongue, Robert B Baird\",\"doi\":\"10.1093/evolut/qpae090\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>How sex chromosomes evolve compared to autosomes remains an unresolved question in population genetics. Most studies focus on only a handful of taxa, resulting in uncertainty over whether observed patterns reflect general processes or idiosyncrasies in particular clades. For example, in female heterogametic (ZW) systems, bird Z chromosomes tend to evolve quickly but not adaptively, while in Lepidopterans they evolve adaptively, but not always quickly. To understand how these observations fit into broader evolutionary patterns, we explore Z chromosome evolution outside of these two well-studied clades. We utilize a publicly available genome, gene expression, population, and outgroup data in the salmon louse Lepeophtheirus salmonis, an important agricultural pest copepod. We find that the Z chromosome is faster evolving than autosomes, but that this effect is driven by increased drift rather than adaptive evolution. Due to high rates of female reproductive failure, the Z chromosome exhibits a slightly lower effective population size than the autosomes which is nonetheless to decrease efficiency of hemizygous selection acting on the Z. These results highlight the usefulness of organismal life history in calibrating population genetic expectations and demonstrate the value of the ever-expanding wealth of publicly available data to help resolve outstanding evolutionary questions.</p>\",\"PeriodicalId\":12082,\"journal\":{\"name\":\"Evolution\",\"volume\":\" \",\"pages\":\"1594-1605\"},\"PeriodicalIF\":3.1000,\"publicationDate\":\"2024-09-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Evolution\",\"FirstCategoryId\":\"93\",\"ListUrlMain\":\"https://doi.org/10.1093/evolut/qpae090\",\"RegionNum\":2,\"RegionCategory\":\"环境科学与生态学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ECOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Evolution","FirstCategoryId":"93","ListUrlMain":"https://doi.org/10.1093/evolut/qpae090","RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ECOLOGY","Score":null,"Total":0}
引用次数: 0
摘要
性染色体进化是群体遗传学的一个复杂分支领域,与常染色体相比,性染色体进化的速度和适应性如何等问题尚未解决。现有知识的一个主要局限是只集中于少数几个类群,导致无法确定观察到的模式是反映了一般过程,还是被广泛研究的类群的特异性。特别是,在鸟类中,雌性异配子(ZW)系统的 Z 染色体倾向于快速进化,但不是适应性进化;而在蝴蝶和蛾类中,Z 染色体倾向于适应性进化,但并不总是快于常染色体。为了了解这两个观察结果如何与更广泛的进化模式相适应,我们探索了这两个研究得比较清楚的支系之外的 Z 染色体进化模式。我们利用公开的高质量基因组、基因表达、种群以及鲑虱 Lepeophtheirus salmonis(一种重要的水产养殖害虫桡足类)的外群数据。我们发现 Z 染色体的进化速度快于常染色体,但这种效应是由漂移增加而非适应性进化驱动的。由于雌性繁殖失败率较高,Z 染色体的有效种群规模仅略低于常染色体,但这足以降低作用于 Z 染色体的半等位选择的效率。这些结果突出了生物体生活史在校准种群遗传预期方面的作用,并证明了不断扩大的现代公开基因组数据的价值,有助于解决悬而未决的进化问题。
Genetic drift drives faster-Z evolution in the salmon louse Lepeophtheirus salmonis.
How sex chromosomes evolve compared to autosomes remains an unresolved question in population genetics. Most studies focus on only a handful of taxa, resulting in uncertainty over whether observed patterns reflect general processes or idiosyncrasies in particular clades. For example, in female heterogametic (ZW) systems, bird Z chromosomes tend to evolve quickly but not adaptively, while in Lepidopterans they evolve adaptively, but not always quickly. To understand how these observations fit into broader evolutionary patterns, we explore Z chromosome evolution outside of these two well-studied clades. We utilize a publicly available genome, gene expression, population, and outgroup data in the salmon louse Lepeophtheirus salmonis, an important agricultural pest copepod. We find that the Z chromosome is faster evolving than autosomes, but that this effect is driven by increased drift rather than adaptive evolution. Due to high rates of female reproductive failure, the Z chromosome exhibits a slightly lower effective population size than the autosomes which is nonetheless to decrease efficiency of hemizygous selection acting on the Z. These results highlight the usefulness of organismal life history in calibrating population genetic expectations and demonstrate the value of the ever-expanding wealth of publicly available data to help resolve outstanding evolutionary questions.
期刊介绍:
Evolution, published for the Society for the Study of Evolution, is the premier publication devoted to the study of organic evolution and the integration of the various fields of science concerned with evolution. The journal presents significant and original results that extend our understanding of evolutionary phenomena and processes.