高分辨率高山植物适应环境变化的局部特异性全基因组特征。

IF 4.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Aude Rogivue, Kevin Leempoel, Annie S. Guillaume, Rimjhim Roy Choudhury, François Felber, Michel Kasser, Stéphane Joost, Christian Parisod, Felix Gugerli
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引用次数: 0

摘要

微进化过程形成了对异质环境的适应性反应,这些影响在物种之间和物种内部都是不同的。然而,基于空间尺度和基因组标记的选择,在多大程度上可以检测到对环境驱动因素的适应特征仍然是未知的。本文研究了高山模式植物Arabis alpina种群中互补类型的基因组变异——单核苷酸多态性(snp)和多态转座因子(TEs),并在两个空间范围水平上研究了局部适应特征。我们将高分辨率(0.5 m)遥感数字高程模型(dem)的环境因素与来自4个种群的304个个体的全基因组测序数据相结合。通过比较在每个地方种群之间检测到的推定适应性位点与同时包括所有种群的区域评估,我们证明了高山桤木对类似数量的非生物变异的反应在很大程度上受当地进化过程的支配。此外,我们发现snp和多态te之间局部适应的最小重叠特征。值得注意的是,适应性候选基因的功能注释揭示了与所研究的非生物因子相关的几个共生相关基因,这可能代表了生物因子的选择压力。我们的研究结果强调了在寻找适应环境变化的特征时考虑不同空间范围和基因组多态性类型的重要性。这些见解提供了微观进化过程的关键信息,可以指导管理决策,以减轻气候变化对高山植物种群的负面影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Locally Specific Genome-Wide Signatures of Adaptation to Environmental Variation at High Resolution in an Alpine Plant

Microevolutionary processes shape adaptive responses to heterogeneous environments, where these effects vary both among and within species. However, it remains largely unknown to which degree signatures of adaptation to environmental drivers can be detected based on the choice of spatial scale and genomic marker. We studied signatures of local adaptation across two levels of spatial extents, investigating complementary types of genomic variants—single-nucleotide polymorphisms (SNPs) and polymorphic transposable elements (TEs)—in populations of the alpine model plant species Arabis alpina . We coupled environmental factors, derived from remote sensed digital elevation models (DEMs) at very high resolution (0.5 m), with whole-genome sequencing data of 304 individuals across four populations. By comparing putatively adaptive loci detected between each local population versus a regional assessment including all populations simultaneously, we demonstrate that responses of A. alpina to similar amounts of abiotic variation are largely governed by local evolutionary processes. Furthermore, we find minimally overlapping signatures of local adaptation between SNPs and polymorphic TEs. Notably, functional annotations of candidate genes for adaptation revealed several symbiosis-related genes associated with the abiotic factors studied, which could represent selective pressures from biotic agents. Our results highlight the importance of considering different spatial extents and types of genomic polymorphisms when searching for signatures of adaptation to environmental variation. Such insights provide key information on microevolutionary processes and could guide management decisions to mitigate negative impacts of climate change on alpine plant populations.

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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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