HLA-DR51 expression failure caused by a two-base deletion at exon 2 of a DRB5 null allele (DRB5*0110N) in a Spanish gypsy family

被引:7
作者
Balas, A
Ocon, P
Vicario, JL
Alonso, A
机构
[1] Reg Ctr Transfus Madrid, Madrid 28009, Spain
[2] Carlos Haya Hosp, Dept Immunol, Malaga, Spain
来源
TISSUE ANTIGENS | 2000年 / 55卷 / 05期
关键词
DR51; DRB5; null allele; HLA; deletion;
D O I
10.1034/j.1399-0039.2000.550513.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Here we describe a new HLA class II null allele at the DRB5 gene. Serologic HLA typing of a Spanish gypsy family rendered the following paternal haplotype: A2-Cblk-B52-Bw4-DR15-DQ5. However, DNA typing demonstrated the presence of a DRB5 gene in the haplotype DRB1*1502-DRB5*0102-DQB1*D5031. Complete DRB5 cDNA sequencing revealed a DRB5*0102 allele with a deletion of two nucleotides at exon 2 (239-240) in codon 80. This change generates a frame shift leading to a stop codon at position 86, and could explain the lack of DR51 protein at the cell surface. This is the second DRB5 nun allele described together with DRB5*0108N, raising the number of HLA alleles with an expression disorder.
引用
收藏
页码:467 / 469
页数:3
相关论文
共 13 条
  • [1] HLA CLASS-I ALLELE (HLA-A2) EXPRESSION DEFECT ASSOCIATED WITH A MUTATION IN ITS ENHANCER-B INVERTED CAT BOX IN 2 FAMILIES
    BALAS, A
    GARCIASANCHEZ, F
    GOMEZREINO, F
    VICARIO, JL
    [J]. HUMAN IMMUNOLOGY, 1994, 41 (01) : 69 - 73
  • [2] BATCHELOR JR, 1989, IMMUNOBIOLOGY HLA, V1, P240
  • [3] Bodmer JG, 1999, HUM IMMUNOL, V60, P361
  • [4] A DNA-based detection and screening system for identifying HLA class I expression variants by sequence-specific primers
    Bunce, M
    Procter, J
    Welsh, KI
    [J]. TISSUE ANTIGENS, 1999, 53 (05): : 498 - 506
  • [5] An intronic mutation responsible for a low level of expression of an HLA-A*24 allele
    Laforet, M
    Froelich, N
    Parissiadis, A
    Bausinger, H
    Pfeiffer, B
    Tongio, MM
    [J]. TISSUE ANTIGENS, 1997, 50 (04): : 340 - 346
  • [6] POLYMORPHISM IN THE REGULATORY REGION OF HLA-DRB GENES CORRELATING WITH HAPLOTYPE EVOLUTION
    LOUIS, P
    ELIAOU, JF
    KERLANCANDON, S
    PINET, V
    VINCENT, R
    CLOT, J
    [J]. IMMUNOGENETICS, 1993, 38 (01) : 21 - 26
  • [7] Marsh SGE, 1998, TISSUE ANTIGENS, V51, P467
  • [8] Filling in the blanks
    Parham, P
    [J]. TISSUE ANTIGENS, 1997, 50 (04): : 318 - 321
  • [9] OLIGONUCLEOTIDE TYPING ANALYSIS FOR THE LINKAGE DISEQUILIBRIUM BETWEEN THE POLYMORPHIC DRB1 AND DRB5 LOCI IN DR2 HAPLOTYPES
    TIERCY, JM
    JEANNET, M
    MACH, B
    [J]. TISSUE ANTIGENS, 1991, 37 (04): : 161 - 164
  • [10] The absence of DR51 in a DRB5-positive individual DR2ES is caused by a null allele (DRB5*0108N)
    Voorter, CEM
    Roeffaers, HET
    duToit, ED
    vandenBergLoonen, EM
    [J]. TISSUE ANTIGENS, 1997, 50 (04): : 326 - 333