对渗透的标准化报告的需求:真核生物研究的见解

IF 3.4 1区 生物学 Q2 EVOLUTIONARY BIOLOGY Evolution Letters Pub Date : 2022-07-25 DOI:10.1002/evl3.294
Andrius J. Dagilis, David Peede, Jenn M. Coughlan, Gaston I. Jofre, Emmanuel R. R. D'Agostino, Heidi Mavengere, Alexander D. Tate, Daniel R. Matute
{"title":"对渗透的标准化报告的需求:真核生物研究的见解","authors":"Andrius J. Dagilis,&nbsp;David Peede,&nbsp;Jenn M. Coughlan,&nbsp;Gaston I. Jofre,&nbsp;Emmanuel R. R. D'Agostino,&nbsp;Heidi Mavengere,&nbsp;Alexander D. Tate,&nbsp;Daniel R. Matute","doi":"10.1002/evl3.294","DOIUrl":null,"url":null,"abstract":"<p>With the rise of affordable next-generation sequencing technology, introgression—or the exchange of genetic materials between taxa—has become widely perceived to be a ubiquitous phenomenon in nature. Although this claim is supported by several keystone studies, no thorough assessment of the frequency of introgression across eukaryotes in nature has been performed to date. In this manuscript, we aim to address this knowledge gap by examining patterns of introgression across eukaryotes. We collated a single statistic, Patterson's <i>D</i>, which can be used as a test for introgression across 123 studies to further assess how taxonomic group, divergence time, and sequencing technology influence reports of introgression. Overall, introgression has mostly been measured in plants and vertebrates, with less attention given to the rest of the Eukaryotes. We find that the most frequently used metrics to detect introgression are difficult to compare across studies and even more so across biological systems due to differences in study effort, reporting standards, and methodology. Nonetheless, our analyses reveal several intriguing patterns, including the observation that differences in sequencing technologies may bias values of Patterson's <i>D</i> and that introgression may differ throughout the course of the speciation process. Together, these results suggest the need for a unified approach to quantifying introgression in natural communities and highlight important areas of future research that can be better assessed once this unified approach is met.</p>","PeriodicalId":48629,"journal":{"name":"Evolution Letters","volume":"6 5","pages":"344-357"},"PeriodicalIF":3.4000,"publicationDate":"2022-07-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9554761/pdf/","citationCount":"9","resultStr":"{\"title\":\"A need for standardized reporting of introgression: Insights from studies across eukaryotes\",\"authors\":\"Andrius J. Dagilis,&nbsp;David Peede,&nbsp;Jenn M. Coughlan,&nbsp;Gaston I. Jofre,&nbsp;Emmanuel R. R. D'Agostino,&nbsp;Heidi Mavengere,&nbsp;Alexander D. Tate,&nbsp;Daniel R. Matute\",\"doi\":\"10.1002/evl3.294\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>With the rise of affordable next-generation sequencing technology, introgression—or the exchange of genetic materials between taxa—has become widely perceived to be a ubiquitous phenomenon in nature. Although this claim is supported by several keystone studies, no thorough assessment of the frequency of introgression across eukaryotes in nature has been performed to date. In this manuscript, we aim to address this knowledge gap by examining patterns of introgression across eukaryotes. We collated a single statistic, Patterson's <i>D</i>, which can be used as a test for introgression across 123 studies to further assess how taxonomic group, divergence time, and sequencing technology influence reports of introgression. Overall, introgression has mostly been measured in plants and vertebrates, with less attention given to the rest of the Eukaryotes. We find that the most frequently used metrics to detect introgression are difficult to compare across studies and even more so across biological systems due to differences in study effort, reporting standards, and methodology. Nonetheless, our analyses reveal several intriguing patterns, including the observation that differences in sequencing technologies may bias values of Patterson's <i>D</i> and that introgression may differ throughout the course of the speciation process. Together, these results suggest the need for a unified approach to quantifying introgression in natural communities and highlight important areas of future research that can be better assessed once this unified approach is met.</p>\",\"PeriodicalId\":48629,\"journal\":{\"name\":\"Evolution Letters\",\"volume\":\"6 5\",\"pages\":\"344-357\"},\"PeriodicalIF\":3.4000,\"publicationDate\":\"2022-07-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9554761/pdf/\",\"citationCount\":\"9\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Evolution Letters\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/evl3.294\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"EVOLUTIONARY BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Evolution Letters","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/evl3.294","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"EVOLUTIONARY BIOLOGY","Score":null,"Total":0}
引用次数: 9

摘要

随着可负担得起的下一代测序技术的兴起,基因渗入——即不同物种之间的遗传物质交换——已被广泛认为是自然界中普遍存在的现象。尽管这一说法得到了几项重要研究的支持,但迄今为止还没有对自然界真核生物的基因渗入频率进行彻底的评估。在这份手稿中,我们的目标是通过检查真核生物的渗入模式来解决这一知识差距。我们整理了一个单一的统计数据,Patterson’s D,它可以用作123项研究的渐渗测试,以进一步评估分类类群、分化时间和测序技术如何影响渐渗报告。总的来说,基因渗入主要是在植物和脊椎动物中测量的,而对其他真核生物的关注较少。我们发现,由于研究努力、报告标准和方法的差异,最常用的检测基因渗入的指标很难在不同的研究中进行比较,在不同的生物系统中更是如此。尽管如此,我们的分析揭示了几个有趣的模式,包括观察到测序技术的差异可能会导致Patterson’s D值的偏差,以及在整个物种形成过程中,基因渗入可能会有所不同。总之,这些结果表明需要一种统一的方法来量化自然群落的渗入,并强调了未来研究的重要领域,一旦这种统一的方法得到满足,就可以更好地评估这些领域。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
A need for standardized reporting of introgression: Insights from studies across eukaryotes

With the rise of affordable next-generation sequencing technology, introgression—or the exchange of genetic materials between taxa—has become widely perceived to be a ubiquitous phenomenon in nature. Although this claim is supported by several keystone studies, no thorough assessment of the frequency of introgression across eukaryotes in nature has been performed to date. In this manuscript, we aim to address this knowledge gap by examining patterns of introgression across eukaryotes. We collated a single statistic, Patterson's D, which can be used as a test for introgression across 123 studies to further assess how taxonomic group, divergence time, and sequencing technology influence reports of introgression. Overall, introgression has mostly been measured in plants and vertebrates, with less attention given to the rest of the Eukaryotes. We find that the most frequently used metrics to detect introgression are difficult to compare across studies and even more so across biological systems due to differences in study effort, reporting standards, and methodology. Nonetheless, our analyses reveal several intriguing patterns, including the observation that differences in sequencing technologies may bias values of Patterson's D and that introgression may differ throughout the course of the speciation process. Together, these results suggest the need for a unified approach to quantifying introgression in natural communities and highlight important areas of future research that can be better assessed once this unified approach is met.

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
Evolution Letters
Evolution Letters EVOLUTIONARY BIOLOGY-
CiteScore
13.00
自引率
2.00%
发文量
35
审稿时长
10 weeks
期刊介绍: Evolution Letters publishes cutting-edge new research in all areas of Evolutionary Biology. Available exclusively online, and entirely open access, Evolution Letters consists of Letters - original pieces of research which form the bulk of papers - and Comments and Opinion - a forum for highlighting timely new research ideas for the evolutionary community.
期刊最新文献
Antibiotic resistance alters the ability of Pseudomonas aeruginosa to invade bacteria from the respiratory microbiome. A biological circuit to anticipate trend. Testing the radiation cascade in postglacial radiations of whitefish and their parasites: founder events and host ecology drive parasite evolution. Sex chromosome turnover in hybridizing stickleback lineages. Adaptive alien genes are maintained amid a vanishing introgression footprint in a sea squirt.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1