Dimorphic primers derived from intron I for use in the molecular typing of HLA-B alleles

被引:80
作者
Cereb, N
Yang, SY
机构
[1] Immunology Program, Mem. Sloan-Kettering Cancer Center, New York, NY
[2] Box 41, Immunology Program, Mem. Sloan-Kettering Cancer Center, New York, NY 10021
来源
TISSUE ANTIGENS | 1997年 / 50卷 / 01期
关键词
HLA class I; polymorphism; DNA typing; intronic sequence;
D O I
10.1111/j.1399-0039.1997.tb02839.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We have identified a dimorphic site in intron 1 of the HLA-B gene. Oligotyping was performed on about 3000 samples using primers derived from this dimorphic site in combination with a locus-specific primer derived from intron 3. The distribution of B-alleles bearing each of the dimorphic sequences was approximately equal. These primers were mutually exclusive and yielded approximately 50% of the heterozygous samples as apparently homozygous in PCR products. Intermediate and almost high-resolution oligotyping of HLA-B alleles was achieved using 35 and 63 hybridization probes, respectively. This dimorphic site will provide a useful tool for other PCR-based HLA-B typing approaches.
引用
收藏
页码:74 / 76
页数:3
相关论文
共 14 条
  • [1] EFFECT OF HLA INCOMPATIBILITY ON GRAFT-VERSUS-HOST DISEASE, RELAPSE, AND SURVIVAL AFTER MARROW TRANSPLANTATION FOR PATIENTS WITH LEUKEMIA OR LYMPHOMA
    ANASETTI, C
    BEATTY, PG
    STORB, R
    MARTIN, PJ
    MORI, M
    SANDERS, JE
    THOMAS, ED
    HANSEN, JA
    [J]. HUMAN IMMUNOLOGY, 1990, 29 (02) : 79 - 91
  • [2] EFFECT OF HLA COMPATIBILITY ON ENGRAFTMENT OF BONE-MARROW TRANSPLANTS IN PATIENTS WITH LEUKEMIA OR LYMPHOMA
    ANASETTI, C
    AMOS, D
    BEATTY, PG
    APPELBAUM, FR
    BENSINGER, W
    BUCKNER, CD
    CLIFT, R
    DONEY, K
    MARTIN, PJ
    MICKELSON, E
    NISPEROS, B
    OQUIGLEY, J
    RAMBERG, R
    SANDERS, JE
    STEWART, P
    STORB, R
    SULLIVAN, KM
    WITHERSPOON, RP
    THOMAS, ED
    HANSEN, JA
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1989, 320 (04) : 197 - 204
  • [3] ANASETTI C, 1994, BONE MARROW TRANSPL, P665
  • [4] HLA-B LOCUS DNA TYPING - DETECTION OF B-ASTERISK-7801 AND 7 ADDITIONAL ALLELES BY BW6-SPECIFIC EXON 2 AMPLIFICATION
    ANDRIEN, M
    TIERCY, JM
    DEFLEUR, V
    BOUILLENNE, C
    TOUNGOUZ, M
    JEANNET, M
    DUPONT, E
    [J]. TISSUE ANTIGENS, 1993, 42 (05): : 480 - 487
  • [5] COMPREHENSIVE, SEROLOGICALLY EQUIVALENT DNA TYPING FOR HLA-B BY PCR USING SEQUENCE-SPECIFIC PRIMERS (PCR-SSP)
    BUNCE, M
    FANNING, GC
    WELSH, KI
    [J]. TISSUE ANTIGENS, 1995, 45 (02): : 81 - 90
  • [6] Cereb N, 1996, J IMMUNOL, V156, P18
  • [7] LOCUS-SPECIFIC AMPLIFICATION OF HLA CLASS-I GENES FROM GENOMIC DNA - LOCUS-SPECIFIC SEQUENCES IN THE FIRST AND 3RD INTRONS OF HLA-A, HLA-B, AND HLA-C ALLELES
    CEREB, N
    MAYE, P
    LEE, S
    KONG, Y
    YANG, SY
    [J]. TISSUE ANTIGENS, 1995, 45 (01): : 1 - 11
  • [8] POPULATION DIVERSITY OF B-LOCUS ALLELES OBSERVED BY HIGH-RESOLUTION DNA TYPING
    FERNANDEZVINA, M
    LAZARO, AM
    SUN, Y
    MILLER, S
    FORERO, L
    STASTNY, P
    [J]. TISSUE ANTIGENS, 1995, 45 (03): : 153 - 168
  • [9] Typing the HLA-B locus by a nested primer approach and oligonucleotide hybridization
    Inamdar, A
    Sintasath, DM
    Husted, L
    Henson, V
    Ng, J
    Hartzman, RJ
    Hurley, CK
    [J]. TISSUE ANTIGENS, 1996, 47 (06): : 519 - 529
  • [10] PRASAD VK, 1996, TISSUE ANTIGENS, V47, P583