Trans-Specific Polymorphisms Between Cryptic Daphnia Species Affect Fitness and Behavior

IF 4.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecular Ecology Pub Date : 2024-12-24 DOI:10.1111/mec.17632
Connor S. Murray, Madison Karram, David J. Bass, Madison Doceti, Dörthe Becker, Joaquin C. B. Nunez, Aakrosh Ratan, Alan O. Bergland
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Abstract

Shared polymorphisms, loci with identical alleles across species, are of unique interest in evolutionary biology as they may represent cases of selection maintaining ancient genetic variation post-speciation, or contemporary selection promoting convergent evolution. In this study, we investigate the abundance of shared polymorphism between two members of the Daphnia pulex species complex. We test whether the presence of shared mutations is consistent with the action of balancing selection or alternative hypotheses such as hybridization, incomplete lineage sorting or convergent evolution. We analyzed over 2,000 genomes from six taxa in the D. pulex species group and examined the prevalence and distribution of shared alleles between the focal species pair, North American and European D. pulex. We show that North American and European D. pulex diverged over 10 million years ago, yet retained tens of thousands of shared polymorphisms. We suggest that the number of shared polymorphisms between North American and European D. pulex cannot be fully explained by hybridization or incomplete lineage sorting alone. We show that most shared polymorphisms could be the product of convergent evolution, that a limited number appear to be old trans-specific polymorphisms, and that balancing selection is affecting convergent and ancient mutations alike. Finally, we provide evidence that a blue wavelength opsin gene with trans-specific polymorphisms has functional effects on behavior and fitness in the wild.

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隐水蚤物种间的跨特异性多态性影响适应性和行为。
共享多态性,即物种间具有相同等位基因的位点,在进化生物学中具有独特的意义,因为它们可能代表了物种形成后选择维持古代遗传变异的情况,或当代选择促进趋同进化的情况。在这项研究中,我们研究了水蚤物种复合体的两个成员之间共享多态性的丰度。我们测试共享突变的存在是否与平衡选择或其他假设(如杂交、不完全谱系排序或趋同进化)的作用一致。本文分析了北美和欧洲白蛉6个类群的2000多个基因组,分析了焦点种对之间共有等位基因的流行和分布。我们的研究表明,北美和欧洲的古猿在1000万年前就已经分化,但仍保留了数以万计的共同多态性。我们认为,单靠杂交或不完整的谱系分类,不能完全解释北美和欧洲龙骨龙骨之间共有多态性的数量。我们表明,大多数共享多态性可能是趋同进化的产物,有限数量的多态性似乎是古老的跨特异性多态性,并且平衡选择对趋同突变和古代突变都有影响。最后,我们提供的证据表明,具有跨特异性多态性的蓝色波长视蛋白基因对野生行为和适应性具有功能影响。
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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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