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
相关论文
共 50 条
  • [31] Genotyping of DNA using sequence-specific methyltransferases followed by immunochemical detection
    López, OJ
    Quintanar, A
    Padhye, NV
    Nelson, M
    JOURNAL OF IMMUNOASSAY & IMMUNOCHEMISTRY, 2003, 24 (01): : 11 - 28
  • [32] Comprehensive HLA-DP typing using polymerase chain reaction with sequence-specific primers and 95 sequence-specific primer mixes
    Gilchrist, FC
    Bunce, M
    Lympany, PA
    Welsh, KI
    du Bois, RM
    TISSUE ANTIGENS, 1998, 51 (01): : 51 - 61
  • [33] Differentiation of Trichinella genotypes by polymerase chain reaction using sequence-specific primers
    Appleyard, GD
    Zarlenga, D
    Pozio, E
    Gajadhar, AA
    JOURNAL OF PARASITOLOGY, 1999, 85 (03) : 556 - 559
  • [34] Typing of HLA-B*15 alleles using sequence-specific primers
    Yu, N
    Ohashi, M
    Alosco, S
    Salazar, M
    Cao, K
    Vina, MF
    Yunis, EJ
    TISSUE ANTIGENS, 1998, 52 (03): : 260 - 269
  • [35] Improved PCR amplification of multiple specific alleles (PAMSA) using internally mismatched primers
    Okimoto, R
    Dodgson, JB
    BIOTECHNIQUES, 1996, 21 (01) : 20 - &
  • [36] Screening apples for OPD20/600 using sequence-specific primers
    Yang, H
    Korban, SS
    THEORETICAL AND APPLIED GENETICS, 1996, 92 (02) : 263 - 266
  • [37] RHD/CE typing by polymerase chain reaction using sequence-specific primers
    Gassner, C
    Schmarda, A
    KilgaNogler, S
    JennyFeldkircher, B
    Rainer, E
    Muller, TH
    Wagner, FF
    Flegel, WA
    Schonitzer, D
    TRANSFUSION, 1997, 37 (10) : 1020 - 1026
  • [38] HPA genotyping by PCR sequence-specific priming (PCR-SSP): A streamlined method for rapid routine investigations
    Cavanagh, G
    Dunn, AN
    Chapman, CE
    Metcalfe, P
    TRANSFUSION MEDICINE, 1997, 7 (01) : 41 - 45
  • [39] Simultaneous genotyping of human platelet antigens (HPA) 1 through 6 using new sequence-specific primers for HPA-5
    Meyer, O
    Hildebrandt, M
    Schulz, B
    Blasczyk, R
    Salama, A
    TRANSFUSION, 1999, 39 (11-12) : 1256 - 1258
  • [40] IMPACT OF HLA-DR TYPING BY PCR AMPLIFICATION WITH SEQUENCE-SPECIFIC PRIMERS ON CADAVERIC RENAL ALLOCATION
    BRYAN, C
    HARRELL, K
    AEDER, M
    LUGER, A
    NELSON, P
    PIERCE, G
    ROSS, G
    SHIELD, C
    WARADAY, B
    HUMAN IMMUNOLOGY, 1993, 37 : 69 - 69