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用于估计微卫星等位基因频率的DNA池评估:以条纹鲈(Morone saxatilis)为例的研究

Evaluation of DNA pooling for the estimation of microsatellite allele frequencies: a case study using striped bass (Morone saxatilis).

作者信息

Skalski Garrick T, Couch Charlene R, Garber Amber F, Weir Bruce S, Sullivan Craig V

机构信息

Department of Ecology and Evolutionary Biology, University of Kansas, Lawrence, Kansas 66045, USA.

出版信息

Genetics. 2006 Jun;173(2):863-75. doi: 10.1534/genetics.105.053702. Epub 2006 Apr 2.

Abstract

Using striped bass (Morone saxatilis) and six multiplexed microsatellite markers, we evaluated procedures for estimating allele frequencies by pooling DNA from multiple individuals, a method suggested as cost-effective relative to individual genotyping. Using moment-based estimators, we estimated allele frequencies in experimental DNA pools and found that the three primary laboratory steps, DNA quantitation and pooling, PCR amplification, and electrophoresis, accounted for 23, 48, and 29%, respectively, of the technical variance of estimates in pools containing DNA from 2-24 individuals. Exact allele-frequency estimates could be made for pools of sizes 2-8, depending on the locus, by using an integer-valued estimator. Larger pools of size 12 and 24 tended to yield biased estimates; however, replicates of these estimates detected allele frequency differences among pools with different allelic compositions. We also derive an unbiased estimator of Hardy-Weinberg disequilibrium coefficients that uses multiple DNA pools and analyze the cost-efficiency of DNA pooling. DNA pooling yields the most potential cost savings when a large number of loci are employed using a large number of individuals, a situation becoming increasingly common as microsatellite loci are developed in increasing numbers of taxa.

摘要

我们使用条纹鲈(Morone saxatilis)和六个多重微卫星标记,评估了通过合并多个个体的DNA来估计等位基因频率的方法,该方法被认为相对于个体基因分型具有成本效益。使用基于矩的估计器,我们估计了实验DNA池中的等位基因频率,发现三个主要的实验室步骤,即DNA定量与合并、PCR扩增和电泳,分别占含有2 - 24个个体DNA的池中估计值技术方差的23%、48%和29%。根据位点的不同,使用整数值估计器可以对大小为2 - 8的池进行精确的等位基因频率估计。大小为12和24的较大池往往会产生有偏差的估计;然而,这些估计的重复检测到了具有不同等位基因组成的池之间的等位基因频率差异。我们还推导了一种使用多个DNA池的哈迪-温伯格不平衡系数的无偏估计器,并分析了DNA合并的成本效益。当使用大量个体检测大量位点时,DNA合并能节省最多的潜在成本,随着越来越多的分类群中开发出微卫星位点,这种情况变得越来越普遍。

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