A simple ABO genotyping by PCR using sequence-specific primers with mismatched nucleotides

被引:11
|
作者
Taki, Takashi [1 ]
Kibayashi, Kazuhiko [1 ]
机构
[1] Tokyo Womens Med Univ, Sch Med, Dept Legal Med, Shinjuku Ku, Tokyo 1628666, Japan
关键词
ABO genotyping; Allele-specific PCR; Pseudo-positive signal; POLYMERASE-CHAIN-REACTION; ALLELE-SPECIFIC PRIMERS; BLOOD-GROUP; POLYMORPHISM; ELECTROPHORESIS; IDENTIFICATION; PHENOTYPES; MUTS;
D O I
10.1016/j.legalmed.2014.02.007
中图分类号
DF [法律]; D9 [法律]; R [医药、卫生];
学科分类号
0301 ; 10 ;
摘要
In forensics, the specific ABO blood group is often determined by analyzing the ABO gene. Among various methods used, PCR employing sequence-specific primers (PCR-SSP) is simpler than other methods for ABO typing. When performing the PCR-SSP, the pseudo-positive signals often lead to errors in ABO typing. We introduced mismatched nucleotides at the second and the third positions from the 3'-end of the primers for the PCR-SSP method and examined whether reliable typing could be achieved by suppressing pseudo-positive signals. Genomic DNA was extracted from nail clippings of 27 volunteers, and the ABO gene was examined with PCR-SSP employing primers with and without mismatched nucleotides. The ABO blood group of the nail clippings was also analyzed serologically, and these results were compared with those obtained using PCR-SSP. When mismatched primers were employed for amplification, the results of the ABO typing matched with those obtained by the serological method. When primers without mismatched nucleotides were used for PCR-SSP, pseudo-positive signals were observed. Thus our method may be used for achieving more reliable ABO typing. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:168 / 172
页数:5
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