Signals of differential introgression in the genome of natural hybrids of Caribbean anoles

Author:

Farleigh Keaka1ORCID,Ascanio Alfredo1ORCID,Farleigh Mackenzie E.1ORCID,Schield Drew R.2ORCID,Card Daren C.34ORCID,Leal Manuel5,Castoe Todd A.6ORCID,Jezkova Tereza1ORCID,Rodríguez‐Robles Javier A.7ORCID

Affiliation:

1. Department of Biology Miami University Oxford Ohio USA

2. Department of Ecology and Evolutionary Biology University of Colorado Boulder Colorado USA

3. Department of Organismic and Evolutionary Biology Harvard University Cambridge Massachusetts USA

4. Museum of Comparative Zoology Harvard University Cambridge Massachusetts USA

5. Division of Biological Sciences University of Missouri Columbia Missouri USA

6. Department of Biology University of Texas, Arlington Arlington Texas USA

7. School of Life Sciences University of Nevada, Las Vegas Las Vegas Nevada USA

Abstract

AbstractHybridization facilitates recombination between divergent genetic lineages and can be shaped by both neutral and selective processes. Upon hybridization, loci with no net fitness effects introgress randomly from parental species into the genomes of hybrid individuals. Conversely, alleles from one parental species at some loci may provide a selective advantage to hybrids, resulting in patterns of introgression that do not conform to random expectations. We investigated genomic patterns of differential introgression in natural hybrids of two species of Caribbean anoles, Anolis pulchellus and A. krugi in Puerto Rico. Hybrids exhibit A. pulchellus phenotypes but possess A. krugi mitochondrial DNA, originated from multiple, independent hybridization events, and appear to have replaced pure A. pulchellus across a large area in western Puerto Rico. Combining genome‐wide SNP datasets with bioinformatic methods to identify signals of differential introgression in hybrids, we demonstrate that the genomes of hybrids are dominated by pulchellus‐derived alleles and show only 10%–20% A. krugi ancestry. The majority of A. krugi loci in hybrids exhibit a signal of non‐random differential introgression and include loci linked to genes involved in development and immune function. Three of these genes (delta like canonical notch ligand 1, jagged1 and notch receptor 1) affect cell differentiation and growth and interact with mitochondrial function. Our results suggest that differential non‐random introgression for a subset of loci may be driven by selection favouring the inheritance of compatible mitochondrial and nuclear‐encoded genes in hybrids.

Funder

University of Miami

National Science Foundation

University of Nevada, Las Vegas

Publisher

Wiley

Subject

Genetics,Ecology, Evolution, Behavior and Systematics

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