McDevitt H O
J Rheumatol Suppl. 1983 Nov;10:50-3.
The availability of cDNA probes for Class I and Class II major histocompatibility complex (MHC) antigens has revealed the existence of more genes in both the Class I and Class II subsets than had been previously detected. The use of restriction endonucleases has demonstrated that restriction enzyme site polymorphisms exist in the flanking sequences for many of the Class I and Class II genes of the MHC. The development of locus specific probes should permit utilization of these restriction site polymorphisms in characterizing particular HLA haplotypes (combinations of HLA A, B, C, DR, DC, and SB) and the availability of allele specific probes, if feasible, would permit direct determination of genotype by DNA hybridization methods. These methods would greatly enhance our understanding of Class I and Class II HLA population genetics, linkage disequilibrium, and association of HLA with susceptibility to autoimmune diseases.
用于I类和II类主要组织相容性复合体(MHC)抗原的cDNA探针的出现,揭示了I类和II类亚群中存在比以前检测到的更多的基因。限制性内切酶的使用表明,MHC的许多I类和II类基因的侧翼序列中存在限制性酶切位点多态性。位点特异性探针的开发应允许利用这些限制性位点多态性来表征特定的HLA单倍型(HLA A、B、C、DR、DC和SB的组合),如果可行的话,等位基因特异性探针的可用性将允许通过DNA杂交方法直接确定基因型。这些方法将极大地增进我们对I类和II类HLA群体遗传学、连锁不平衡以及HLA与自身免疫性疾病易感性关联的理解。