混合图谱揭示剑尾鱼杂交种多重有丝核不亲和性的证据。

IF 3.9 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Nemo V Robles, Benjamin M Moran, María José Rodríguez Barrera, Gaston I Jofre, Theresa Gunn, Erik N K Iverson, Sofia Beskid, John J Baczenas, Alisa Sedghifar, Peter Andolfatto, Daniel L Powell, Yaniv Brandvain, Justin C Havird, Gil G Rosenthal, Molly Schumer
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引用次数: 0

摘要

基因流动的障碍是如何在近亲物种之间产生的,这是进化生物学中最古老的问题之一。进化生物学的经典模型预测,在分化谱系的基因组中,变异之间的负遗传相互作用,即杂交不相容,将降低杂种的生存能力或育性。这些相互作用的遗传结构及其产生的进化路径对杂交不亲和性作为物种间基因流动障碍的有效性具有深远的影响。虽然这些问题已经用理论方法研究了几十年,但直到最近才有可能绘制出大量杂交不相容的基因图谱。本研究利用剑尾鱼(Xiphophorus)自然杂交种群的混合作图,确定了涉及线粒体和核基因组遗传相互作用的杂交不亲和性。我们发现基因组中至少有9个区域与有丝核不相容有关。这些不相容涉及核基因组与X. malinche线粒体、X. birchmanni线粒体或两者之间的相互作用。此外,它们经历的选择强度和它们在自然杂交群体中限制基因流动的程度各不相同。我们的研究结果加深了对自然杂交物种中对抗不亲和性选择的复杂结构的理解,并强调了有丝核相互作用在近亲物种之间生殖障碍进化中的重要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Admixture Mapping Reveals Evidence for Multiple Mitonuclear Incompatibilities in Swordtail Fish Hybrids.

How barriers to gene flow arise between closely related species is one of the oldest questions in evolutionary biology. Classic models in evolutionary biology predict that negative epistatic interactions between variants in the genomes of diverged lineages, known as hybrid incompatibilities, will reduce viability or fertility in hybrids. The genetic architecture of these interactions and the evolutionary paths through which they arise have profound implications for the efficacy of hybrid incompatibilities as barriers to gene flow between species. While these questions have been studied using theoretical approaches for several decades, only recently has it become possible to genetically map larger numbers of hybrid incompatibilities. Here, we use admixture mapping in natural hybrid populations of swordtail fish (Xiphophorus) to identify hybrid incompatibilities involving genetic interactions between the mitochondrial and nuclear genomes. We find that at least nine regions of the genome are involved in mitonuclear incompatibilities. These incompatibilities involve interactions between the nuclear genome and the X. malinche mitochondria, the X. birchmanni mitochondria, or both. Moreover, they vary in the strength of selection they experience and the degree to which they limit gene flow in natural hybrid populations. Our results build a deeper understanding of the complex architecture of selection against incompatibilities in naturally hybridising species and highlight an important role of mitonuclear interactions in the evolution of reproductive barriers between closely related species.

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来源期刊
Molecular Ecology
Molecular Ecology 生物-进化生物学
CiteScore
8.40
自引率
10.20%
发文量
472
审稿时长
1 months
期刊介绍: Molecular Ecology publishes papers that utilize molecular genetic techniques to address consequential questions in ecology, evolution, behaviour and conservation. Studies may employ neutral markers for inference about ecological and evolutionary processes or examine ecologically important genes and their products directly. We discourage papers that are primarily descriptive and are relevant only to the taxon being studied. Papers reporting on molecular marker development, molecular diagnostics, barcoding, or DNA taxonomy, or technical methods should be re-directed to our sister journal, Molecular Ecology Resources. Likewise, papers with a strongly applied focus should be submitted to Evolutionary Applications. Research areas of interest to Molecular Ecology include: * population structure and phylogeography * reproductive strategies * relatedness and kin selection * sex allocation * population genetic theory * analytical methods development * conservation genetics * speciation genetics * microbial biodiversity * evolutionary dynamics of QTLs * ecological interactions * molecular adaptation and environmental genomics * impact of genetically modified organisms
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