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[基因库的选择性结构。II. 使用F(ST)统计量的标准方法]

[Selective structure of the gene pool. II. Standard method using F(ST) statistics].

作者信息

Balanovskaia E V, Nurbaev S D

机构信息

Institute of Clinical Genetics, Research Center for Medical Genetics, Russian Academy of Medical Sciences, Moscow, Russia.

出版信息

Genetika. 1998 Sep;34(9):1307-21.

PMID:9879018
Abstract

A new approach to the description of the selective structure of the gene pool that is determined by the type and intensity of selection for individual genes is suggested. Selective pressure is defined based on the heterogeneity of the interpopulation diversity index FST. It is assumed that a significant difference between the estimated heterogeneity for the ith gene FST(i) and the selectively neutral interpopulation differentiation of the gene pool (Fe) indicate an effect of selection on the ith gene. In order to reveal such significant differences, empirical FST(i) distributions for the human gene pools of all parts of the world and five subregions of northeastern Eurasia were approximated by different theoretical distributions. It was demonstrated that only beta-distributions yielded a good approximation of the empirical FST(i) estimations in all studied gene pools. Based on the beta-approximations, confidence intervals for FST were calculated. These intervals allowed the genes to be divided into three classes of selective structure. Class NEUTRAL comprised genes that were assumed to be selectively neutral (FST(i) approximately equal to Fe); classes LOWER DIFF and SUPER DIFF comprised selectively important genes with significantly decreased (FST(i) < Fe) and increased (FST(i) > Fe) differentiation, respectively. Positions of 80 immunologically important biochemical markers were determined in the selective structure of the gene pools of six regions of the world: Europe, Asia, Africa, Australia, America, and northwestern Eurasia. The suggested method of estimating selective structure can be used if FST = Fe, where Fe is a selectively neutral variation of genes. Fe = 4NeMe + 1)-1; the main conditions for the use of this method are the following assumptions: (1) the genetic process is stationary and (2) the effective population size (Ne), the migration rate (Me), and the selection rate (S) are constant in time and space. If these conditions are not met, a correction (numeric resampling) is required.

摘要

提出了一种新方法来描述由单个基因的选择类型和强度所决定的基因库选择结构。基于群体间多样性指数FST的异质性来定义选择压力。假设第i个基因的估计异质性FST(i)与基因库的选择性中性群体间分化(Fe)之间存在显著差异,表明选择对第i个基因有影响。为了揭示这种显著差异,用不同的理论分布对世界所有地区以及欧亚大陆东北部五个次区域的人类基因库的经验FST(i)分布进行了近似。结果表明,只有β分布能很好地近似所有研究基因库中的经验FST(i)估计值。基于β近似值,计算了FST的置信区间。这些区间可将基因分为三类选择结构。中性类包括被认为是选择性中性的基因(FST(i)约等于Fe);较低分化类和超分化类分别包括选择性重要基因,其分化显著降低(FST(i) < Fe)和增加(FST(i) > Fe)。在世界六个地区(欧洲、亚洲、非洲、澳大利亚、美洲和欧亚大陆西北部)的基因库选择结构中确定了80个免疫重要生化标记的位置。如果FST = Fe,其中Fe是基因的选择性中性变异,则可以使用所建议的估计选择结构的方法。Fe = (4NeMe + 1)-1;使用该方法的主要条件是以下假设:(1)遗传过程是稳定的,(2)有效种群大小(Ne)、迁移率(Me)和选择率(S)在时间和空间上是恒定的。如果不满足这些条件,则需要进行校正(数值重采样)。

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