Fernandez-Viña M A, Gao X J, Moraes M E, Moraes J R, Salatiel I, Miller S, Tsai J, Sun Y P, An J B, Layrisse Z
Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas 75235-8886.
Immunogenetics. 1991;34(5):299-312. doi: 10.1007/BF00211994.
The use of polymerase chain reaction (PCR) and oligonucleotide hybridization offers a new approach for the definition of HLA class II alleles. It has been possible to determine 43 alleles of DRB1, four of DRB3, two of DRB4, four of DRB5, eight of DQA1, and 14 of DQB1. These alleles are inherited together in members of families and form closely associated groups which are found repeatedly and in characteristic patterns in different populations. We have determined the HLA class II alleles and analyzed their association in 431 healthy unrelated subjects including 161 North American Caucasians, 53 Latin Americans, 61 Blacks, 88 Chinese, and 68 Israeli Jews. For-locus haplotypes (DRB1; DRB3/4/5; DQA1; DQB1) were derived from 79 B cell lines and the analysis of segregation in 34 nuclear families. The B-cell lines yielded 37 and the families showed the same, and 20 other, haplotypic combinations. In addition to these 57 haplotypes, associated alleles were assigned in the unrelated panels following certain rules. The resulting haplotypes were assigned to groups known to share associated alleles. The groups were: 1) DR1, DR2, and DRw10 (13 haplotypes); 2) DR3 and DRw6 (26 haplotypes); 3) DR5 and DRw8 (24 haplotypes); 4) DR4, DR7, and DR9 (24 haplotypes). Their distribution in populations with different ethnic backgrounds was analyzed. The expressed DRB4 allele and its null mutant were determined by PCR and oligonucleotide hybridization. The different DR7 haplotypes resulting from these determinations were analyzed in a panel of 130 North American Caucasoids. This comprehensive analysis of class II HLA haplotypes in human populations should be useful in understanding the role of these genes and in various applications including anthropology, disease susceptibility, and transplantation of allogeneic organs and tissues.
聚合酶链反应(PCR)和寡核苷酸杂交技术的应用为确定HLA - II类等位基因提供了一种新方法。现已能够确定DRB1的43个等位基因、DRB3的4个等位基因、DRB4的2个等位基因、DRB5的4个等位基因、DQA1的8个等位基因以及DQB1的14个等位基因。这些等位基因在家族成员中共同遗传,并形成紧密相关的组群,在不同人群中以特征性模式反复出现。我们已确定了431名健康无关个体的HLA - II类等位基因,并分析了它们之间的关联,这些个体包括161名北美白种人、53名拉丁美洲人、61名黑人、88名中国人和68名以色列犹太人。对于基因座单倍型(DRB1;DRB3/4/5;DQA1;DQB1),是从79个B淋巴细胞系以及对34个核心家庭的分离分析中得出的。B淋巴细胞系产生了37种单倍型,家庭分析显示了相同的以及另外20种单倍型组合。除了这57种单倍型外,还按照特定规则在无关个体样本中确定了相关等位基因。所得到的单倍型被归入已知共享相关等位基因的组群中。这些组群分别是:1)DR1、DR2和DRw10(13种单倍型);2)DR3和DRw6(2种单倍型);3)DR5和DRw8(24种单倍型);4)DR4、DR7和DR9(24种单倍型)。分析了它们在不同种族背景人群中的分布情况。通过PCR和寡核苷酸杂交确定了表达的DRB4等位基因及其无效突变体。在一组130名北美白种人中分析了由这些测定结果产生的不同DR7单倍型。对人类群体中II类HLA单倍型的这种全面分析,对于理解这些基因的作用以及在包括人类学、疾病易感性和异体器官与组织移植等各种应用中应是有用的。