构建可增强 Argus X-12 试剂盒鉴别能力的 13 个位点 X-STR 多重 PCR 系统:在马来人口中的应用。

IF 1.3 4区 医学 Q3 MEDICINE, LEGAL
Kiyoshi Minaguchi , Michinaga Samejima , Phrabhakaran Nambiar , Yu Kaneko , Eriko Ochiai , Yu Kakimoto , Motoki Osawa
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引用次数: 0

摘要

X 染色体上紧密相连的标记群对于检测涉及 X-STR 传播的复杂亲缘关系非常有用。Argus X-12 试剂盒是一种独特的市售试剂盒,可获得由 3 个标记组成的 4 个连锁群(LG)的单倍型。虽然已有许多用于法医目的的人群数据报告,但在东亚人群中,LG1 与 LG2、3 和 4 的分辨能力存在差异,如果提高后几组的分辨能力,该试剂盒的数据将更加有用。因此,对于使用本试剂盒找到的某些连接组数据的匹配结果,为了提高识别能力,我们额外引入了 13 个 X-STR 位点,并建立了一种可以使用 25 个位点数据进行比较的方法。13 个 X-STR 位点为 LG2、3 和 4 各增加了两个位点数据,还在一次多重 PCR 中为 LG2 和 3 以及 LG3 和 4 之间增加了两个密切相关群(CLG)数据。该方法对一个马来种群的评估显示,LG2、3 和 4 中不同单倍型的频率增加了 33.0-42.6%,独特单倍型的频率增加了 45.4-59.2%。新增的 3 个基因座和 4 个基因座 CLG 的单倍型多样性值分别为 0.9838 和 0.9939,这有助于提高鉴别力和预测 X 染色体上的重组位置。虽然我们是在日本受试者中测试这些位点,但这一系统对马来人群也很有用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Construction of 13-locus X-STR multiplex PCR system that reinforces Argus X-12 kit discrimination capacity: Application to the Malay population

Closely linked groups of markers on the X chromosome are very useful for testing complex kinship relationships involving X-STR transmission. The Argus X-12 kit, a unique commercially available kit, can obtain haplotypes of 4 linkage groups (LGs) consisting of 3 markers. Although many population data have been reported for forensic purposes, differences in discrimination ability exist between LG1 and LG2, 3, and 4 in East Asian populations, and the data of this kit would become more useful if the discrimination ability of the latter groups were increased. Therefore, for matches found using this kit for some linkage group data, then to increase the identification ability, we additionally introduced 13 X-STR loci and established a method allowing comparison using data from 25 loci. The 13X-STRs add two locus data to each of LG2, 3, and 4, and also add two closely linked group (CLG) data between LG2 and 3 and LG3 and 4 in one multiplex PCR. Assessment of this method for a Malay population for which data by Argus X-12 had already been reported showed that the frequencies of distinct haplotypes in LG2, 3, and 4 were increased by 33.0–42.6 %, and frequencies of unique haplotypes increased by 45.4–59.2 %. The respective haplotype diversity values of the additional 3-locus and 4-locus CLGs were 0.9838 and 0.9939, which helps to improve discriminatory power and to predict recombination locations on the X chromosome. Although we have been testing these loci with Japanese subjects, this system would also be useful for the Malay population.

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来源期刊
Legal Medicine
Legal Medicine Nursing-Issues, Ethics and Legal Aspects
CiteScore
2.80
自引率
6.70%
发文量
119
审稿时长
7.9 weeks
期刊介绍: Legal Medicine provides an international forum for the publication of original articles, reviews and correspondence on subjects that cover practical and theoretical areas of interest relating to the wide range of legal medicine. Subjects covered include forensic pathology, toxicology, odontology, anthropology, criminalistics, immunochemistry, hemogenetics and forensic aspects of biological science with emphasis on DNA analysis and molecular biology. Submissions dealing with medicolegal problems such as malpractice, insurance, child abuse or ethics in medical practice are also acceptable.
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