DQB1*0202 and the new DQB1*0203 allele: A fourth pair of DQB1 alleles differing only at codon 57

被引:12
作者
Olerup, O
AldenerCannava, A
FogdellHahn, A
Getty, RR
Wagenknecht, DR
McIntyre, JA
机构
[1] HUDDINGE HOSP,KAROLINSKA INST,DIV CLIN IMMUNOL,S-14186 HUDDINGE,SWEDEN
[2] METHODIST HOSP INDIANA,METHODIST CTR REPROD & TRANSPLANTAT IMMUNOL,INDIANAPOLIS,IN 46202
来源
TISSUE ANTIGENS | 1997年 / 49卷 / 03期
关键词
evolution; haplotype; histocompatibility testing; HLA-DQB1; nucleotide sequencing;
D O I
10.1111/j.1399-0039.1997.tb02750.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Amino acid 57 of DQ beta chains is of functional importance as it influences peptide binding, is part of B and T cell epitopes, and is associated with susceptibility and resistance to insulin-dependent diabetes mellitus and humoral immunodeficiencies. Polymorphism of codon 57 is conserved in primates and in HLA class II B genes implying that balancing selection operates on this residue. Previously, three DQB1 allele pairs have been described, that only differ at residue 57. In an African-American Black individual with the HLA phenotype A23,30;B58,63;Cw6;DR18, 12;DR52;DQ5,2, we found a fourth example of this dimorphism; the new DQB1*0203 allele, that was identical to DQB1*0202 except for codon 57, which encodes aspartic acid and alanine respectively in the two alleles. The class II haplotype carrying the new allele was deduced to be DRB1*0302,DRB3*0101,DQA1*05011,DQB1*0203.
引用
收藏
页码:271 / 273
页数:3
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