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通过对来自多个物种的基因组多态性和分化的贝叶斯分析来鉴定自然选择的谱系特异性靶标。

Identifying Lineage-Specific Targets of Natural Selection by a Bayesian Analysis of Genomic Polymorphisms and Divergence from Multiple Species.

机构信息

CAS Key Laboratory of Genomic and Precision Medicine, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing, China.

School of Future Technology, University of Chinese Academy of Sciences, Beijing, China.

出版信息

Mol Biol Evol. 2019 Jun 1;36(6):1302-1315. doi: 10.1093/molbev/msz046.

DOI:10.1093/molbev/msz046
PMID:30840083
Abstract

We present a method that jointly analyzes the polymorphism and divergence sites in genomic sequences of multiple species to identify the genes under natural selection and pinpoint the occurrence time of selection to a specific lineage of the species phylogeny. This method integrates population genetics models using a Bayesian Poisson random field framework and combines information over all gene loci to boost the power for detecting selection. The method provides posterior distributions of the fitness effects of each gene along with parameters associated with the evolutionary history, including the species divergence time and effective population size of external species. The results of simulations demonstrate that our method achieves a high power to identify genes under positive selection for a wide range of selection intensity and provides reasonably accurate estimates of the population genetic parameters. The proposed method is applied to genomic sequences of humans, chimpanzees, gorillas, and orangutans and identifies a list of lineage-specific targets of positive selection. The positively selected genes in the human lineage are enriched in pathways of gene expression regulation, immune system and metabolism, etc. Our analysis provides insights into natural evolution in the coding regions of humans and great apes and thus serves as a basis for further molecular and functional studies.

摘要

我们提出了一种方法,该方法联合分析了多个物种基因组序列中的多态性和分歧位点,以鉴定受自然选择影响的基因,并确定选择发生的时间在物种系统发育的特定谱系上。该方法使用贝叶斯泊松随机场框架整合了群体遗传学模型,并结合了所有基因座的信息,以提高检测选择的能力。该方法提供了每个基因的适应度效应的后验分布,以及与进化历史相关的参数,包括物种分歧时间和外部物种的有效种群大小。模拟结果表明,我们的方法在广泛的选择强度下具有很高的识别正选择基因的能力,并提供了种群遗传参数的合理准确估计。该方法应用于人类、黑猩猩、大猩猩和猩猩的基因组序列,鉴定出一系列谱系特异性的正选择靶标。人类谱系中的正选择基因富集在基因表达调控、免疫系统和新陈代谢等途径中。我们的分析为人类和大猿类的编码区域的自然进化提供了深入的了解,因此为进一步的分子和功能研究奠定了基础。

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