Coupling of twelve putative chromosomal inversions maintains a strong barrier to gene flow between snail ecotypes

Author:

Le Moan Alan12ORCID,Stankowski Sean3ORCID,Rafajlović Marina1ORCID,Ortega-Martinez Olga1ORCID,Faria Rui45ORCID,Butlin Roger K16ORCID,Johannesson Kerstin1ORCID

Affiliation:

1. Department of Marine Sciences, Tjärnö Marine Laboratory, University of Gothenburg , 452 96 Strömstad , Sweden

2. Adaptation et Diversité en Milieu Marin, UMR7144, Station Biologique de Roscoff, Sorbonne Université , 29680 Roscoff , France

3. Institute of Science and Technology Austria , 3 21 44 Klosterneuburg , Austria

4. CIBIO, Centro de Investigação em Biodiversidade e Recursos Genéticos, InBIO Laboratório Associado, Campus de Vairão, Universidade do Porto , 4485-661 Vairão , Portugal

5. BIOPOLIS Program in Genomics, Biodiversity and Land Planning, CIBIO , Campus de Vairão, 4485-661 Vairão , Portugal

6. Ecology and Evolutionary Biology, School of Biosciences, University of Sheffield , Sheffield S10 2TN , United Kingdom

Abstract

Abstract Chromosomal rearrangements can lead to the coupling of reproductive barriers, but whether and how they contribute to the completion of speciation remains unclear. Marine snails of the genus Littorina repeatedly form hybrid zones between populations segregating for multiple inversion arrangements, providing opportunities to study their barrier effects. Here, we analyzed 2 adjacent transects across hybrid zones between 2 ecotypes of Littorina fabalis (“large” and “dwarf”) adapted to different wave exposure conditions on a Swedish island. Applying whole-genome sequencing, we found 12 putative inversions on 9 of 17 chromosomes. Nine of the putative inversions reached near differential fixation between the 2 ecotypes, and all were in strong linkage disequilibrium. These inversions cover 20% of the genome and carry 93% of divergent single nucleotide polymorphisms (SNPs). Bimodal hybrid zones in both transects indicated that the 2 ecotypes of Littorina fabalis maintain their genetic and phenotypic integrity following contact. The bimodality reflects the strong coupling between inversion clines and the extension of the barrier effect across the whole genome. Demographic inference suggests that coupling arose during a period of allopatry and has been maintained for > 1,000 generations after secondary contact. Overall, this study shows that the coupling of multiple chromosomal inversions contributes to strong reproductive isolation. Notably, 2 of the putative inversions overlap with inverted genomic regions associated with ecotype differences in a closely related species (Littorina saxatilis), suggesting the same regions, with similar structural variants, repeatedly contribute to ecotype evolution in distinct species.

Funder

Swedish Research Council

Leverhulme Trust

Portuguese Science Foundation

Publisher

Oxford University Press (OUP)

Reference68 articles.

1. Hybridization and speciation;Abbott,2013

2. The dynamics of hybrid zones;Barton,1979

3. Genetic analysis of hybrid zones;Barton,1993

4. Adaptation, speciation and hybrid zones;Barton,1989

5. The coupling hypothesis: why genome scans may fail to map local adaptation genes;Bierne,2011

Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3