Holbeck S L, Nepom G T
Immunogenetics. 1986;24(4):251-8. doi: 10.1007/BF00364529.
The HLA genetic region consists of a large multigene complex which includes a number of highly homologous alpha and beta genes encoding class II polypeptides, clustered in three major loci, DP, DQ, and DR. Analysis of genomic polymorphisms at each of these loci is of considerable interest due to the role of particular structural polymorphisms in immune function, but this analysis has been hampered by difficulty in distinguishing between such highly homologous loci. We have identified locus-specific and exon-specific class II gene sequences in order to produce synthetic oligonucleotide probes which hybridize specifically to DQ beta genes. Two such oligonucleotide probes are described which are specific for the beta 1 and beta 2 exons of DQ (DC) beta, which identify DQ beta genes in digests of cellular DNA and which can be used to characterize restriction sites flanking the two oligonucleotide-specific regions. By sequentially hybridizing these probes in modified Southern analyses, we have been able to generate a tentative "restriction map" of a newly identified DQ beta allele from digests of total genomic DNA. This oligonucleotide mapping technique discriminates between two HLA-DQw3+ alleles, DQ3.1 and DQ3.2, permitting the recognition of structural polymorphisms with DQ beta which are highly associated with type I diabetes mellitus.
HLA基因区域由一个大型多基因复合体组成,其中包括许多编码II类多肽的高度同源的α和β基因,这些基因聚集在三个主要位点,即DP、DQ和DR。由于特定结构多态性在免疫功能中的作用,对这些位点中每个位点的基因组多态性进行分析具有相当大的意义,但这种分析因难以区分这些高度同源的位点而受到阻碍。我们已经鉴定出基因座特异性和外显子特异性的II类基因序列,以便生产能与DQβ基因特异性杂交的合成寡核苷酸探针。本文描述了两种这样的寡核苷酸探针,它们对DQ(DC)β的β1和β2外显子具有特异性,能在细胞DNA消化物中识别DQβ基因,并且可用于鉴定两个寡核苷酸特异性区域侧翼的限制性酶切位点。通过在改良的Southern分析中依次杂交这些探针,我们已经能够从总基因组DNA消化物中生成一个新鉴定的DQβ等位基因的初步“限制性图谱”。这种寡核苷酸图谱技术能够区分两种HLA-DQw3+等位基因,即DQ3.1和DQ3.2,从而能够识别与I型糖尿病高度相关的DQβ结构多态性。