Gogolin K J, Kolaga V J, Baker L, Lisak R P, Zmijewski C M, Spielman R S
Department of Human Genetics, University of Pennsylvania School of Medicine, Philadelphia 19104-6072.
Ann Hum Genet. 1989 Oct;53(4):327-38. doi: 10.1111/j.1469-1809.1989.tb01802.x.
We have used the HLA-DQB1 gene as a Southern hybridization probe with TaqI-digested genomic DNA in a study of 600 haplotypes from unrelated individuals and have characterized HLA-DQB1 RFLP patterns associated with the DR specificities DR1-DRw10 and DN1. For six of the specificities (DR2, 4, w6, 7, w8 and 9), we have also identified subtypes (multiple DQB1 band patterns). In a previous study (Cox et al. 1988), we identified RFLPs and subtypes with a DRB1 probe. Using the present results from DQB1 RFLPs to supplement those from DRB1 RFLPs, it was possible to discriminate among all the DR specificities with the exception of a minority of DR7 and DR9 subtypes. A comparison of DQB1 and DRB1 subtypes in the same subjects showed strong linkage disequilibrium for subtypes of some but not all DR specificities. We have also determined the allele frequencies of the DQB1 subtypes in controls and in patients with insulin-dependent diabetes mellitus (IDDM) or multiple sclerosis (MS). A consideration of subtypes in patients and controls indicated that for most DR specificities, neither IDDM nor MS was more strongly associated with any of the DQB1 subtypes than with the serologically defined DR antigens. The exceptions were the DQB1 patterns corresponding to the DQw3.2 subtype of DR4 and the rarer subtype of DR2, which were found in higher frequency in IDDM patients, as has been previously reported.
我们在一项对600个无关个体单倍型的研究中,将HLA - DQB1基因用作Southern杂交探针,与经TaqI酶切的基因组DNA杂交,并对与DR特异性DR1 - DRw10和DN1相关的HLA - DQB1限制性片段长度多态性(RFLP)模式进行了特征分析。对于其中六种特异性(DR2、4、w6、7、w8和9),我们还鉴定出了亚型(多种DQB1条带模式)。在之前的一项研究(Cox等人,1988年)中,我们用DRB1探针鉴定了RFLP和亚型。利用目前DQB1 RFLP的结果来补充DRB1 RFLP的结果,除了少数DR7和DR9亚型外,能够区分所有的DR特异性。对同一受试者的DQB1和DRB1亚型进行比较,结果显示部分而非全部DR特异性的亚型之间存在强连锁不平衡。我们还测定了对照组以及胰岛素依赖型糖尿病(IDDM)或多发性硬化症(MS)患者中DQB1亚型的等位基因频率。对患者和对照组的亚型进行分析表明,对于大多数DR特异性而言,IDDM和MS与任何DQB1亚型的关联都不比与血清学定义的DR抗原的关联更强。例外情况是与DR4的DQw3.2亚型相对应的DQB1模式以及DR2的较罕见亚型,正如之前所报道的,它们在IDDM患者中出现的频率更高。