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基于多重 PCR 的 Alu 插入多态性基因分型鉴定日本人群个体。

Multiplex PCR-based Alu insertion polymorphisms genotyping for identifying individuals of Japanese ethnicity.

机构信息

Department of Legal Medicine, Asahikawa Medical University, 2-1-1-1 Midorigaoka-Higashi, Asahikawa 078-8510, Japan.

出版信息

Genomics. 2012 Apr;99(4):227-32. doi: 10.1016/j.ygeno.2012.01.004. Epub 2012 Jan 26.

Abstract

Discrimination of Alu insertions is a useful tool for geographic ancestry analysis, and is usually performed by Alu element amplification and agarose gel electrophoresis. Here, we have developed a new fluorescence-based method for multiple Alu genotyping in forensic identification. Allele frequencies were determined in 70 Japanese individuals, and we selected 30 polymorphic Alu insertions. Three primers were designed for each Alu locus to discriminate alleles using the 3-6 bp differences in amplicon sizes. Furthermore, we classified the amplification primers for the 30 loci into three different sets, and PCR using each set of primers provided 10 loci fragments ranging from 50 to 137 bp. Based on population data, the probability of incorrectly assigning a match was 3.7×10(-13). Three independent amplifications and subsequent capillary electrophoresis enabled the sensitive genotyping of small amounts of DNA, indicating that this method is suitable for identifying individuals of Japanese ethnicity.

摘要

Alu 插入的判别是地理起源分析的有用工具,通常通过 Alu 元件扩增和琼脂糖凝胶电泳进行。在这里,我们开发了一种新的荧光法,用于法医鉴定中的多个 Alu 基因分型。在 70 名日本人个体中确定了等位基因频率,我们选择了 30 个多态性 Alu 插入。针对每个 Alu 基因座设计了 3 个引物,通过扩增子大小的 3-6 bp 差异来区分等位基因。此外,我们将 30 个基因座的扩增引物分为三组,每组引物的 PCR 提供了 10 个从 50 到 137 bp 的片段。基于群体数据,错误分配匹配的概率为 3.7×10(-13)。三个独立的扩增和随后的毛细管电泳使少量 DNA 的敏感基因分型成为可能,表明该方法适用于鉴定日本人种的个体。

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Two problematic human polymorphic Alu insertions.两个有问题的人类多态性Alu插入序列。
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