如何预测物种演化过程中的基因流动?时间、空间、形态和气候的相对作用

IF 4.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Jeffrey W Streicher, Shea M Lambert, Fausto R Méndez de la Cruz, Norberto Martínez-Méndez, Uri Omar García-Vázquez, Adrián Nieto Montes de Oca, John J Wiens
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引用次数: 0

摘要

限制种群间基因流动的过程是物种分化的基础。在这里,我们建立了一个简单的框架,用于研究形态、气候生态位、时间和空间的差异是否会导致种群和物种间基因流动的减少。我们将这一框架应用于一个模型系统,该系统涉及主要分布于墨西哥东北部的棘蜥支系(Sceloporus),在密切相关的物种和种群之间,棘蜥支系在形态和栖息地方面表现出惊人的差异。我们利用来自 152 个个体的 RADseq 数据为该类群建立了新的时间校准系统发育。该系统发育确定了 12 个推定的物种级支系,包括至少两个未描述的物种。然后,我们估算了 21 对地理上相邻的物种和种群之间的基因流水平。我们还估算了这些物种对之间形态和气候生态位变量的差异,以及差异时间和地理距离。利用贝叶斯广义线性模型,我们发现成对种系之间的基因流与它们之间的分化时间和形态分化(不相关)呈负相关,而与地理距离或气候分化无关。这里使用的框架可用于研究其他许多拥有基因组数据但缺乏生殖隔离直接数据的生物的物种分化。我们还在这个系统中发现了其他一些有趣的模式,包括在两个不同的非姊妹物种中,从颜色更暗淡的沙漠祖先平行演化出惊人相似的山地蓝红形态。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
What Predicts Gene Flow During Speciation? The Relative Roles of Time, Space, Morphology and Climate.

The processes that restrict gene flow between populations are fundamental to speciation. Here, we develop a simple framework for studying whether divergence in morphology, climatic niche, time and space contribute to reduced gene flow among populations and species. We apply this framework to a model system involving a clade of spiny lizards (Sceloporus) occurring mostly in northeastern Mexico, which show striking variation in morphology and habitat among closely related species and populations. We developed a new time-calibrated phylogeny for the group using RADseq data from 152 individuals. This phylogeny identified 12 putative species-level clades, including at least two undescribed species. We then estimated levels of gene flow among 21 geographically adjacent pairs of species and populations. We also estimated divergence in morphological and climatic niche variables among these same pairs, along with divergence times and geographic distances. Using Bayesian generalised linear models, we found that gene flow between pairs of lineages is negatively related to divergence time and morphological divergence among them (which are uncorrelated), and not to geographic distance or climatic divergence. The framework used here can be applied to study speciation in many other organisms having genomic data but lacking direct data on reproductive isolation. We also found several other intriguing patterns in this system, including the parallel evolution of a strikingly similar montane blue-red morph from more dull-coloured desert ancestors within two different, nonsister 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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