The genomes of Darwin's primroses reveal chromosome‐scale adaptive introgression and differential permeability of species boundaries

Author:

Stubbs Rebecca L.1ORCID,Theodoridis Spyros2ORCID,Mora‐Carrera Emiliano1ORCID,Keller Barbara1ORCID,Potente Giacomo1ORCID,Yousefi Narjes1ORCID,Jay Paul3ORCID,Léveillé‐Bourret Étienne4ORCID,Choudhury Rimjhim Roy5ORCID,Celep Ferhat6ORCID,Kochjarová Judita7ORCID,Conti Elena1ORCID

Affiliation:

1. Department of Systematic and Evolutionary Botany University of Zurich Zurich 8008 Switzerland

2. Senckenberg Biodiversity and Climate Research Centre (SBiK‐F) Frankfurt am Main 60325 Germany

3. Center for GeoGenetics University of Copenhagen Copenhagen 1350 Denmark

4. Département de Sciences Biologiques, Institut de Recherche en Biologie Végétale (IRBV) Université de Montréal Montreal QC H1X 2B2 Canada

5. Department of Biology University of Fribourg Fribourg 1700 Switzerland

6. Department of Biology, Faculty of Arts and Sciences Kırıkkale University Kırıkkale 71450 Turkey

7. Department of Phytology, Faculty of Forestry Technical University in Zvolen Zvolen 96001 Slovak Republic

Abstract

Summary Introgression is an important source of genetic variation that can determine species adaptation to environmental conditions. Yet, definitive evidence of the genomic and adaptive implications of introgression in nature remains scarce. The widespread hybrid zones of Darwin's primroses (Primula elatior, Primula veris, and Primula vulgaris) provide a unique natural laboratory for studying introgression in flowering plants and the varying permeability of species boundaries. Through analysis of 650 genomes, we provide evidence of an introgressed genomic region likely to confer adaptive advantage in conditions of soil toxicity. We also document unequivocal evidence of chloroplast introgression, an important precursor to species‐wide chloroplast capture. Finally, we provide the first evidence that the S‐locus supergene, which controls heterostyly in primroses, does not introgress in this clade. Our results contribute novel insights into the adaptive role of introgression and demonstrate the importance of extensive genomic and geographical sampling for illuminating the complex nature of species boundaries.

Funder

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung

Publisher

Wiley

Subject

Plant Science,Physiology

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