Replicate geographic transects across a hybrid zone reveal parallelism and differences in the genetic architecture of reproductive isolation.

IF 3.7 1区 生物学 Q2 EVOLUTIONARY BIOLOGY
Evolution Letters Pub Date : 2025-05-07 eCollection Date: 2025-08-01 DOI:10.1093/evlett/qraf009
Georgy Semenov, Haley Kenyon, Erik Funk, William Anderson, Michael McQuillan, Joan Spinelli, Austin Russell, Noel Martinez, Alex Van Huynh, Alana Alexander, Rena Schweizer, Ethan Linck, Zachary Cheviron, Matt Carling, Timothy Roth, Mark Robbins, Amber Rice, Scott Taylor
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引用次数: 0

Abstract

Determining the genetic architecture of traits involved in adaptation and speciation is one of the key components of understanding the evolutionary mechanisms behind biological diversification. Hybrid zones provide a unique opportunity to use genetic admixture to identify traits and loci contributing to partial reproductive barriers between taxa. Many studies have focused on the temporal dynamics of hybrid zones, but geographical variation in hybrid zones that span distinct ecological contexts has received less attention. We address this knowledge gap by analyzing hybridization and introgression between black-capped and Carolina chickadees in two geographically remote transects across their extensive hybrid zone, one located in eastern and one in central North America. Previous studies demonstrated that this hybrid zone is moving northward as a result of climate change but is staying consistently narrow due to selection against hybrids. In addition, the hybrid zone is moving ~5× slower in central North America compared to more eastern regions, reflecting continent-wide variation in the rate of climate change. We use whole genome sequencing of 259 individuals to assess whether variation in the rate of hybrid zone movement is reflected in patterns of hybridization and introgression, and which genes and genomic regions show consistently restricted introgression in distinct ecological contexts. Our results highlight substantial similarities between geographically remote transects and reveal large Z-linked chromosomal rearrangements that generate measurable differences in the degree of gene flow between transects. We further use simulations and analyses of climatic data to examine potential factors contributing to continental-scale nuances in selection pressures. We discuss our findings in the context of speciation mechanisms and the importance of sex chromosome inversions in chickadees and other species.

在杂交带中复制地理样带揭示了生殖隔离遗传结构的相似性和差异性。
确定与适应和物种形成有关的性状的遗传结构是理解生物多样化背后的进化机制的关键组成部分之一。杂交带提供了一个独特的机会,利用遗传混合来识别有助于分类群之间部分生殖障碍的性状和位点。许多研究都集中在杂交带的时间动态上,但杂交带在不同生态环境下的地理变化却很少受到关注。我们通过分析黑冠山雀和卡罗莱纳山雀在两个地理上遥远的横断面上的杂交和渐渗现象来解决这一知识差距,一个位于北美东部,一个位于北美中部。先前的研究表明,由于气候变化,这个杂交区正在向北移动,但由于对杂交的选择,它一直保持狭窄。此外,北美中部混合带的移动速度比东部地区慢约5倍,反映了气候变化速度在整个大陆范围内的变化。我们使用259个个体的全基因组测序来评估杂交带迁移率的变化是否反映在杂交和渗入模式中,以及哪些基因和基因组区域在不同的生态环境中表现出持续的限制性渗入。我们的研究结果突出了地理上遥远的样条之间的实质性相似性,并揭示了大的z连锁染色体重排,这些重排在样条之间的基因流动程度上产生了可测量的差异。我们进一步使用气候数据的模拟和分析来检查导致大陆尺度选择压力细微差别的潜在因素。我们在物种形成机制的背景下讨论了我们的发现,以及性别染色体倒位在山雀和其他物种中的重要性。
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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.
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