利用目标富集和线粒体基因组撇取方法研究美洲鼠兔(Ochotona princeps)在大陆范围内的种内适应性变异证据。

IF 4.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecular Ecology Pub Date : 2024-10-19 DOI:10.1111/mec.17557
Zachery M Farrand, Kurt E Galbreath, Katherine C Teeter
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引用次数: 0

摘要

山地景观带来了一系列非生物挑战,推动了生物的适应性进化。这些适应性会促进栖息地的特化,从而增加因环境变化而灭绝的风险。例如,内热物种较高的新陈代谢率可能有助于提高耐寒性,同时限制耐热性。在这里,我们利用对气候敏感的美洲鼠兔(Ochotona princeps),测试了北美西部中山区环境梯度中种内适应性变异的证据。我们利用之前关于鼠兔适应性的研究成果,生成了一个定制的核靶标富集设计,对数百个与寒冷、缺氧和饮食解毒相关的候选基因进行测序。我们还采用了 "基因组撇脂 "方法对线粒体DNA进行测序。通过基因型-环境关联测试,我们发现了与不同人群的海拔和温度变化相关的罕见基因组变异。在线粒体基因中,我们发现了选择信号的种内变异和氨基酸属性平衡常数的显著变化,这可能与电子传递链的效率有关。这些结果表明,王子鸥之间存在着复杂的适应性变异动态,其品系和种群已经适应了独特的区域条件。一些最明显的选择信号出现在包括大盆地地区鼠兔在内的一个遗传系中,这也是最近发生局部灭绝的地方,并凸显了在环境变化过程中丧失适应性等位基因的风险。
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Evidence of Intraspecific Adaptive Variation in the American Pika (Ochotona princeps) on a Continental Scale Using a Target Enrichment and Mitochondrial Genome Skimming Approach.

Montane landscapes present an array of abiotic challenges that drive adaptive evolution amongst organisms. These adaptations can promote habitat specialisation, which may heighten the risk of extirpation from environmental change. For example, higher metabolic rates in an endothermic species may contribute to heightened cold tolerance, whilst simultaneously limiting heat tolerance. Here, using the climate-sensitive American pika (Ochotona princeps), we test for evidence of intraspecific adaptive variation amongst environmental gradients across the Intermountain West of North America. We leveraged results from previous studies on pika adaptation to generate a custom nuclear target enrichment design to sequence several hundred candidate genes related to cold, hypoxia and dietary detoxification. We also applied a 'genome skimming' approach to sequence mitochondrial DNA. Using genotype-environment association tests, we identified rare genomic variants associated with elevation and temperature variation amongst populations. Amongst mitochondrial genes, we identified intraspecific variation in selective signals and significant changes to the amino acid property equilibrium constant, which may relate to electron transport chain efficiency. These results illustrate a complex dynamic of adaptive variation amongst O. princeps where lineages and populations have adapted to unique regional conditions. Some of the clearest signals of selection were in a genetic lineage that includes pikas of the Great Basin region, which is also where recent localised extirpations have taken place and highlights the risk of losing adaptive alleles during environmental change.

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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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