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AS-PCR技术检测20个mtDNA SNP位点及单倍型频率

聂燕钗 张晨 刘亚楠 黄江平 焦海涛 吴丹 周怀谷

法医学杂志Issue(2):96-100,109,6.
法医学杂志Issue(2):96-100,109,6.DOI:10.3969/j.issn.1004-5619.2014.02.005

AS-PCR技术检测20个mtDNA SNP位点及单倍型频率

AS-PCR Assay for 20 mtDNA SNP Typing and Haplotype Frequency

聂燕钗 1张晨 2刘亚楠 2黄江平 2焦海涛 3吴丹 2周怀谷2

作者信息

  • 1. 复旦大学上海医学院法医学系,上海 200032
  • 2. 上海市公安局物证鉴定中心 法医物证学现场应用技术公安部重点实验室 上海市现场物证重点实验室,上海 200083
  • 3. 上海锦博生物技术有限公司,上海 200433
  • 折叠

摘要

Abstract

Objective To develop a multiplex allele-specific PCR (AS-PCR) assay with three-color fluo-rescence labeling for mitochondrial DNA (mtDNA) SNP typing. Methods Based on the principle of AS-PCR, the primer sets were designed for 20 SNP located on the coding region of mtDNA and divided in-to 2 groups labeled with FAM and HEX fluorescence, respectively. A primer set included two forward (reverse) allelic specific primers with different sizes and a generic reverse (forward) primer. Blood sam-ples from 200 unrelated individuals were analyzed by AS-PCR and capillary electrophoresis. Three ran-dom samples at least for each SNP site were examined and verified by direct sequencing. The haplotype frequency was investigated. Results Distinct electropherograms of 200 blood samples were obtained suc-cessfully. The typing results of direct sequencing were identical to those obtained from AS-PCR. The minimum detectable DNA concentration was 0.2 pg under the system of 10μL. The sensitivity of the DNA concentrations ranged from 0.5 to 5 pg. The 200 individuals were assigned into 15 haplotype, and the haplotype diversity was 0.906 0. Conclusion AS-PCR is a simple, rapid and efficient method for mtDNA SNP typing, and can be applied to forensic practice.

关键词

法医遗传学/多态性,单核苷酸/等位基因/聚合酶链反应/单倍型

Key words

forensic genetics/polymorphism, single nucleotide/alleles/polymerase chain reaction/haplotype

分类

社会科学

引用本文复制引用

聂燕钗,张晨,刘亚楠,黄江平,焦海涛,吴丹,周怀谷..AS-PCR技术检测20个mtDNA SNP位点及单倍型频率[J].法医学杂志,2014,(2):96-100,109,6.

基金项目

公安部科技基础工作专项资助项目 ()

法医学杂志

OACHSSCDCSCDCSTPCDMEDLINE

1004-5619

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