Construction of SNP-STR Multiplex Amplification System with Genetic Markers and Its Forensic Application.
10.12116/j.issn.1004-5619.2020.03.005
- Author:
Qiu Yue WANG
1
;
Yi Wen YANG
1
;
Yue Yan CAO
1
;
Qiang ZHU
1
;
Yu Guo HUANG
1
;
Yu Han HU
1
;
Yi Jun ZHOU
1
;
Xi LI
1
;
Yi Fan WEI
1
;
Pan Yin SHU
1
;
Yu Fang WANG
1
;
Ji ZHANG
1
Author Information
1. West China School of Basic Medical Sciences & Forensic Medicine, Sichuan University, Chengdu 610041, China.
- Publication Type:Journal Article
- Keywords:
forensic genetics;
polymorphism, single nucleotide;
short tandem repeat;
allele specific-polymerase chain reaction;
mixed DNA
- MeSH:
China;
DNA Fingerprinting;
DNA Primers;
Gene Frequency;
Genetic Markers;
Humans;
Microsatellite Repeats;
Polymerase Chain Reaction;
Polymorphism, Single Nucleotide
- From:
Journal of Forensic Medicine
2020;36(3):316-315
- CountryChina
- Language:English
-
Abstract:
Objective To select and develop a SNP-STR multiplex amplification system with genetic markers compatible with current STR databases. To understand its genetic polymorphisms in Sichuan Han population and its application value in DNA mixture analysis. Methods Based on the STR genetic markers in commercial kits, SNPs adjacent to these STR markers were selected to be SNP-STR genetic markers. A SNP-STR multiplex amplification system with genetic markers based on allele-specific amplification was constructed using allele-specific amplification primers. The genetic polymorphism of the system in the Sichuan Han population was investigated and the efficiency of systems with different numbers of loci to detect the two individual DNA mixture samples was evaluated. Results An allele-specific multiplex amplification system constituted of 13 SNP-STR genetic markers was selected and constructed. In Sichuan Han population, the heterozygosity of each locus ranged from 0.76 to 0.88, and the combined discrimination power reached 0.999 999 999 999 999 968. In the analysis of the two individual DNA mixture samples： for single-locus amplification, the genotype of the minor components can still be detected when the mixture ratio reaches 1 000∶1; for multiple loci multiplex amplification, the maximum mixture ratio can reach 500∶1. As the number of loci in the system increased, the detection efficiency of the minor components in the DNA mixture decreased. Conclusion SNP-STR genetic markers have a higher polymorphism than STR. The multiplex amplification system made of SNP-STR genetic markers has a better analysis efficiency for mixed samples than traditional STR multiplex amplification system.
