Beneficial reversal of dominance maintains a large-effect resistance polymorphism under fluctuating insecticide selection

IF 13.9 1区 生物学 Q1 ECOLOGY
Marianthi Karageorgi, Anastasia S. Lyulina, Mark C. Bitter, Egor Lappo, Sharon I. Greenblum, Zach K. Mouza, Caitlynn T. Tran, Andy V. Huynh, Hayes Oken, Paul Schmidt, Dmitri A. Petrov
{"title":"Beneficial reversal of dominance maintains a large-effect resistance polymorphism under fluctuating insecticide selection","authors":"Marianthi Karageorgi, Anastasia S. Lyulina, Mark C. Bitter, Egor Lappo, Sharon I. Greenblum, Zach K. Mouza, Caitlynn T. Tran, Andy V. Huynh, Hayes Oken, Paul Schmidt, Dmitri A. Petrov","doi":"10.1038/s41559-025-02853-x","DOIUrl":null,"url":null,"abstract":"<p>Large-effect standing genetic variation is commonly found in natural populations and must be maintained in the face of directional natural selection. Theory suggests that under fluctuating selective pressures, beneficial reversal of dominance—where alleles are dominant when beneficial and recessive when deleterious—can strongly stabilize large-effect polymorphisms. However, empirical evidence for this mechanism remains limited because testing requires measurements of selection and dominance in fitness in natural conditions. Here we investigate large-effect fitness polymorphisms at the <i>Ace</i> locus of <i>Drosophila melanogaster</i> that confer insecticide resistance and persist at intermediate frequencies worldwide. By combining laboratory and large-scale field mesocosm experiments with insecticide manipulation and mathematical modelling, we show that the benefits of the resistant <i>Ace</i> alleles are dominant in pesticide-rich environments, while their fitness costs are recessive in pesticide-free environments. We further show that temporally fluctuating insecticide selection generates chromosome-scale genomic perturbations at sites linked to the resistant <i>Ace</i> alleles. Overall, our results suggest that beneficial reversal of dominance under temporally fluctuating selection might plausibly contribute to the maintenance of functional genetic variation and, by stabilizing large frequency fluctuations, impact long-range patterns of genomic variation.</p>","PeriodicalId":18835,"journal":{"name":"Nature ecology & evolution","volume":"34 1","pages":""},"PeriodicalIF":13.9000,"publicationDate":"2025-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nature ecology & evolution","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1038/s41559-025-02853-x","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ECOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Large-effect standing genetic variation is commonly found in natural populations and must be maintained in the face of directional natural selection. Theory suggests that under fluctuating selective pressures, beneficial reversal of dominance—where alleles are dominant when beneficial and recessive when deleterious—can strongly stabilize large-effect polymorphisms. However, empirical evidence for this mechanism remains limited because testing requires measurements of selection and dominance in fitness in natural conditions. Here we investigate large-effect fitness polymorphisms at the Ace locus of Drosophila melanogaster that confer insecticide resistance and persist at intermediate frequencies worldwide. By combining laboratory and large-scale field mesocosm experiments with insecticide manipulation and mathematical modelling, we show that the benefits of the resistant Ace alleles are dominant in pesticide-rich environments, while their fitness costs are recessive in pesticide-free environments. We further show that temporally fluctuating insecticide selection generates chromosome-scale genomic perturbations at sites linked to the resistant Ace alleles. Overall, our results suggest that beneficial reversal of dominance under temporally fluctuating selection might plausibly contribute to the maintenance of functional genetic variation and, by stabilizing large frequency fluctuations, impact long-range patterns of genomic variation.

Abstract Image

在波动的杀虫剂选择下,有利的优势反转维持了大效抗性多态性
大效应站立性遗传变异在自然种群中普遍存在,在定向自然选择中必须保持遗传变异。理论表明,在波动的选择压力下,有利的优势逆转——等位基因在有利时是显性的,在有害时是隐性的——可以强有力地稳定大效应多态性。然而,这种机制的经验证据仍然有限,因为测试需要测量自然条件下适应性的选择和优势。在这里,我们研究了黑腹果蝇Ace位点的大效应适应度多态性,这种多态性赋予了杀虫剂抗性,并在世界范围内以中等频率持续存在。通过将实验室和大规模田间中生态实验与杀虫剂操作和数学模型相结合,我们发现抗性Ace等位基因的优势在杀虫剂丰富的环境中是显性的,而它们的适应度成本在无杀虫剂的环境中是隐性的。我们进一步表明,杀虫剂选择的暂时波动会在与抗性Ace等位基因相关的位点产生染色体尺度的基因组扰动。总的来说,我们的研究结果表明,在暂时波动的选择下,有利的优势逆转可能有助于维持功能性遗传变异,并通过稳定大频率波动,影响基因组变异的长期模式。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Nature ecology & evolution
Nature ecology & evolution Agricultural and Biological Sciences-Ecology, Evolution, Behavior and Systematics
CiteScore
22.20
自引率
2.40%
发文量
282
期刊介绍: Nature Ecology & Evolution is interested in the full spectrum of ecological and evolutionary biology, encompassing approaches at the molecular, organismal, population, community and ecosystem levels, as well as relevant parts of the social sciences. Nature Ecology & Evolution provides a place where all researchers and policymakers interested in all aspects of life's diversity can come together to learn about the most accomplished and significant advances in the field and to discuss topical issues. An online-only monthly journal, our broad scope ensures that the research published reaches the widest possible audience of scientists.
×
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:604180095
Book学术官方微信