一个 "大物种 "属的系统发生组学揭示了岛屿系统中猖獗的不完全世系分类、基因流动和线粒体捕获现象

Jenna McCullough, Chad Eliason, Shannon J Hackett, Corinne E Myers, Michael J Andersen
{"title":"一个 \"大物种 \"属的系统发生组学揭示了岛屿系统中猖獗的不完全世系分类、基因流动和线粒体捕获现象","authors":"Jenna McCullough, Chad Eliason, Shannon J Hackett, Corinne E Myers, Michael J Andersen","doi":"10.1101/2024.08.28.610082","DOIUrl":null,"url":null,"abstract":"The flora and fauna of island systems, especially those in the Indo-Pacific, are renowned for their high diversification rates and outsized contribution to the development of evolutionary theories. The total diversity of geographic radiations of many Indo-Pacific fauna is often incompletely sampled in phylogenetic studies due to the difficulty in obtaining single island endemic forms across the Pacific and the relatively poor performance of degraded DNA when using museum specimens for inference of evolutionary relationships. New methods for production and analysis of genome-wide datasets sourced from degraded DNA are facilitating insights into the complex evolutionary histories of these influential island faunas. Here, we leverage whole genome resequencing (20X average coverage) and extensive sampling of all taxonomic diversity within Todiramphus kingfishers, a rapid radiation of largely island endemic \"Great Speciators.\" We find that whole genome datasets do not outright resolve the evolutionary relationships of this clade: four types of molecular markers (UCEs, BUSCOs, SNPs, and mtDNA) and tree building methods did not find a single well-supported and concordant species-level topology. We then uncover evidence of widespread incomplete lineage sorting and both ancient and contemporary gene flow and demonstrate how these factors contribute to conflicting evolutionary histories. Our complete taxonomic sampling allowed us to further identify a novel case of mitochondrial capture between two allopatric species, suggesting a potential historical (but since lost) hybrid zone as islands were successively colonized. Taken together, these results highlight how increased genomic and taxon sampling can reveal complex evolutionary patterns in rapid island radiations.","PeriodicalId":501575,"journal":{"name":"bioRxiv - Zoology","volume":"173 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-08-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Phylogenomics of a genus of \\\"Great Speciators\\\" reveals rampant incomplete lineage sorting, gene flow, and mitochondrial capture in island systems\",\"authors\":\"Jenna McCullough, Chad Eliason, Shannon J Hackett, Corinne E Myers, Michael J Andersen\",\"doi\":\"10.1101/2024.08.28.610082\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The flora and fauna of island systems, especially those in the Indo-Pacific, are renowned for their high diversification rates and outsized contribution to the development of evolutionary theories. The total diversity of geographic radiations of many Indo-Pacific fauna is often incompletely sampled in phylogenetic studies due to the difficulty in obtaining single island endemic forms across the Pacific and the relatively poor performance of degraded DNA when using museum specimens for inference of evolutionary relationships. New methods for production and analysis of genome-wide datasets sourced from degraded DNA are facilitating insights into the complex evolutionary histories of these influential island faunas. Here, we leverage whole genome resequencing (20X average coverage) and extensive sampling of all taxonomic diversity within Todiramphus kingfishers, a rapid radiation of largely island endemic \\\"Great Speciators.\\\" We find that whole genome datasets do not outright resolve the evolutionary relationships of this clade: four types of molecular markers (UCEs, BUSCOs, SNPs, and mtDNA) and tree building methods did not find a single well-supported and concordant species-level topology. We then uncover evidence of widespread incomplete lineage sorting and both ancient and contemporary gene flow and demonstrate how these factors contribute to conflicting evolutionary histories. Our complete taxonomic sampling allowed us to further identify a novel case of mitochondrial capture between two allopatric species, suggesting a potential historical (but since lost) hybrid zone as islands were successively colonized. Taken together, these results highlight how increased genomic and taxon sampling can reveal complex evolutionary patterns in rapid island radiations.\",\"PeriodicalId\":501575,\"journal\":{\"name\":\"bioRxiv - Zoology\",\"volume\":\"173 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-08-29\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"bioRxiv - Zoology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1101/2024.08.28.610082\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"bioRxiv - Zoology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1101/2024.08.28.610082","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

岛屿系统,尤其是印度洋-太平洋岛屿系统的动植物群以其高度多样化率和对进化理论发展的巨大贡献而闻名于世。在系统发育研究中,由于难以获得太平洋地区的单岛特有形式,以及使用博物馆标本推断进化关系时降解 DNA 的性能相对较差,许多印度洋-太平洋动物群的地理辐射总多样性往往取样不全。利用降解 DNA 制作和分析全基因组数据集的新方法有助于深入了解这些具有影响力的岛屿动物群的复杂进化历史。在这里,我们利用全基因组重测序(20 倍平均覆盖率)和对 Todiramphus 翠鸟内所有分类多样性的广泛采样,这是一种主要由岛屿特有的 "大物种 "快速辐射而成的动物。我们发现,全基因组数据集并不能彻底解决该支系的进化关系:四种类型的分子标记(UCEs、BUSCOs、SNPs 和 mtDNA)和树构建方法都没有发现一个支持良好且一致的物种级拓扑结构。随后,我们发现了普遍存在的不完整的种系分类以及古代和当代基因流动的证据,并展示了这些因素是如何导致相互矛盾的进化史的。我们完整的分类取样使我们能够进一步确定两个异源物种之间线粒体捕获的新案例,这表明随着岛屿被陆续殖民,潜在的历史(但已消失)杂交区。综上所述,这些结果突显了增加基因组和分类群取样如何揭示快速岛屿辐射中复杂的进化模式。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Phylogenomics of a genus of "Great Speciators" reveals rampant incomplete lineage sorting, gene flow, and mitochondrial capture in island systems
The flora and fauna of island systems, especially those in the Indo-Pacific, are renowned for their high diversification rates and outsized contribution to the development of evolutionary theories. The total diversity of geographic radiations of many Indo-Pacific fauna is often incompletely sampled in phylogenetic studies due to the difficulty in obtaining single island endemic forms across the Pacific and the relatively poor performance of degraded DNA when using museum specimens for inference of evolutionary relationships. New methods for production and analysis of genome-wide datasets sourced from degraded DNA are facilitating insights into the complex evolutionary histories of these influential island faunas. Here, we leverage whole genome resequencing (20X average coverage) and extensive sampling of all taxonomic diversity within Todiramphus kingfishers, a rapid radiation of largely island endemic "Great Speciators." We find that whole genome datasets do not outright resolve the evolutionary relationships of this clade: four types of molecular markers (UCEs, BUSCOs, SNPs, and mtDNA) and tree building methods did not find a single well-supported and concordant species-level topology. We then uncover evidence of widespread incomplete lineage sorting and both ancient and contemporary gene flow and demonstrate how these factors contribute to conflicting evolutionary histories. Our complete taxonomic sampling allowed us to further identify a novel case of mitochondrial capture between two allopatric species, suggesting a potential historical (but since lost) hybrid zone as islands were successively colonized. Taken together, these results highlight how increased genomic and taxon sampling can reveal complex evolutionary patterns in rapid island radiations.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信