Jing Wang, Nathaniel R. Street, Eung-Jun Park, Jianquan Liu, P?r K. Ingvarsson
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引用次数: 25
摘要
增加我们对进化过程如何驱动变异的基因组景观的理解是更好地理解物种形成的基因组后果的基础。然而,尽管大多数森林树种具有重要的全球生态和经济意义,但它们的种内和种间变异的全基因组模式尚未得到充分研究。本文利用4种杨树的全基因组重测序数据,重建了杨树的人口统计学历史,并研究了种内和种间的多样性和分化模式。以毛杨(Populus trichocarpa)为外群,进一步推测了三种白杨(Populus tremula, Populus davidiana和Populus tremuloides)的谱系关系,并估计了三种白杨在整个基因组中的古代遗传渐近程度。我们的研究结果显示,这些模式在基因组中有很大的变化,这种变化可以通过局部重组率和功能元件的密度来预测。这意味着循环选择和内在基因组特征之间的相互作用在很长一段时间内戏剧性地塑造了基因组景观。此外,我们的发现提供了证据,除了背景选择,近期的积极选择和长期的平衡选择也在物种形成过程中形成全基因组变异模式的关键组成部分。
Evidence for widespread selection in shaping the genomic landscape during speciation of Populus
Increasing our understanding of how evolutionary processes drive the genomic landscape of variation is fundamental to a better understanding of the genomic consequences of speciation. However, genome-wide patterns of within- and between- species variation have not been fully investigated in most forest tree species despite their global ecological and economic importance. Here, we use whole-genome resequencing data from four Populus species spanning the speciation continuum to reconstruct their demographic histories and investigate patterns of diversity and divergence within and between species. Using Populus trichocarpa as an outgroup species, we further infer the genealogical relationships and estimate the extent of ancient introgression among the three aspen species (Populus tremula, Populus davidiana and Populus tremuloides) throughout the genome. Our results show substantial variation in these patterns along the genomes with this variation being strongly predicted by local recombination rates and the density of functional elements. This implies that the interaction between recurrent selection and intrinsic genomic features has dramatically sculpted the genomic landscape over long periods of time. In addition, our findings provide evidence that, apart from background selection, recent positive selection and long-term balancing selection have also been crucial components in shaping patterns of genome-wide variation during the speciation process.
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