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一种用于检测中国汉族人群SCN5A基因中45种突变的SNaPshot检测法。

A SNaPshot assay for detection of 45 mutations in the SCN5A gene in the Chinese Han Population.

作者信息

Wang Jiaqi, Wang Xudong, Ma Zhihua, Yun Keming, Liu Jinding, Chen Deqing, Liu Zidong, Shi Jie, Li Zeqin, Gao Cairong, Du Qiuxiang, Zhang Gengqian

机构信息

School of Forensic Medicine, Shanxi Medical University, Taiyuan, P. R. China.

Forensic Science Engineering Research Center of Universities in Chongqing, Chongqing, P. R. China.

出版信息

Electrophoresis. 2018 Sep;39(17):2270-2276. doi: 10.1002/elps.201800096. Epub 2018 Jul 3.

Abstract

Sudden cardiac death (SCD) occurs frequently in forensic practice and results in no visible pathological changes that can be detected in an autopsy. In recent years, the genetic background has been emphasized when examining SCD cases. The aim of this study is to establish a feasible system to detect SCD-related genes for forensic DNA laboratories. Forty-five reported SCD-associated SNPs from sodium voltage-gated channel alpha subunit 5 (SCN5A) were considered in our experiment. We established a SNaPshot assay for the typing of 45 SNPs using multiplex PCR and the minisequencing technique. Two multiplex PCRs were performed and optimized to cover 14 and 16 DNA fragments. The SCD victims came from the Chinese Han population residing in Shanxi and Chongqing provinces and were examined and compared with a non-SCD group and with normal healthy individuals. A missense mutation at rs1805124 (H558R) was detected in the Chinese Han population in this study. A SNaPshot assay can be performed in any forensic DNA laboratory and would be capable of meeting the increasing demand for SCD detection. This method would also be beneficial for screening at-risk in family members of SCD victims.

摘要

心脏性猝死(SCD)在法医实践中经常发生,尸检时未发现可检测到的明显病理变化。近年来,在检查SCD病例时,遗传背景受到了重视。本研究的目的是为法医DNA实验室建立一个可行的系统来检测与SCD相关的基因。我们的实验考虑了来自钠电压门控通道α亚基5(SCN5A)的45个已报道的与SCD相关的单核苷酸多态性(SNP)。我们建立了一种SNaPshot检测方法,使用多重PCR和微测序技术对45个SNP进行分型。进行了两次多重PCR并进行优化,以覆盖14个和16个DNA片段。SCD受害者来自居住在山西和重庆的中国汉族人群,并与非SCD组和正常健康个体进行了检查和比较。在本研究的中国汉族人群中检测到rs1805124(H558R)处的一个错义突变。SNaPshot检测方法可在任何法医DNA实验室进行,能够满足对SCD检测日益增长的需求。该方法对于筛查SCD受害者家庭成员中的高危个体也将是有益的。

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