Toyoda H, Redford A, Magalong D
Department of Medicine, Cedars-Sinai Medical Center, UCLA School of Medicine 90048.
Dis Markers. 1992 Jan-Feb;10(1):7-18.
The DNA methylation state of the 5'-regulatory region of human HLA-DQ beta genes was examined. Two restriction enzymes were utilized to detect methylated (meCG) dinucleotides in the 5'-regulatory region of the DQ-beta genes: the restriction enzyme Msp I, which recognizes CCGG and CmeCGG, and Hpa II recognizes only the unmethylated CG sequence. DNA samples were prepared from 95 HLA-typed individuals including 40 B-lymphoblastoid cell lines and peripheral blood leukocytes of 55 individuals. Of these samples, 20 were from parents of individuals with insulin-dependent diabetes. Allele specific methylation was observed in particular DR-associated DQ-beta gene alleles. The DQw8 (DQw3.2) allele, most DQw7 (DQw3.1) alleles, and the DR3-associated DQw2 allele were all unmethylated. The parental methylation state was stably transmitted to offspring. Because these DQ alleles are highly associated with several autoimmune diseases, our results raise the possibility that the regulation of expression of these particular DQ-beta alleles might be different from that of other alleles, and that the 5'-regulatory DNA sequences of these particular DQ beta alleles may be responsible for, or contribute to, susceptibility to autoimmune diseases.
对人类HLA-DQβ基因5'-调控区的DNA甲基化状态进行了检测。使用两种限制性内切酶来检测DQ-β基因5'-调控区中的甲基化(meCG)二核苷酸:限制性内切酶Msp I可识别CCGG和CmeCGG,而Hpa II仅识别未甲基化的CG序列。从95名进行了HLA分型的个体中制备了DNA样本,其中包括40个B淋巴母细胞系以及55名个体的外周血白细胞。在这些样本中,有20个来自胰岛素依赖型糖尿病患者的父母。在特定的与DR相关的DQ-β基因等位基因中观察到了等位基因特异性甲基化。DQw8(DQw3.2)等位基因、大多数DQw7(DQw3.1)等位基因以及与DR3相关的DQw2等位基因均未甲基化。亲代的甲基化状态稳定地传递给了子代。由于这些DQ等位基因与多种自身免疫性疾病高度相关,我们的结果提示,这些特定DQ-β等位基因的表达调控可能与其他等位基因不同,并且这些特定DQβ等位基因的5'-调控DNA序列可能导致或促成自身免疫性疾病的易感性。