Jackson D G, Capra J D
Center for Diabetes Research, University of Texas Southwestern Medical Center at Dallas 75235-9048.
Proc Natl Acad Sci U S A. 1993 Dec 1;90(23):11079-83. doi: 10.1073/pnas.90.23.11079.
It has been previously demonstrated that individuals with certain DR alleles have an increased relative risk of developing insulin-dependent diabetes mellitus (IDDM). The disease association is even stronger with certain DQ alleles but there is little association with DP providing a boundary of disease association to the 430 kb between DQ and DP. The recently described TAP (transporter associated with antigen processing) genes have been mapped approximately midway between DP and DQ. Therefore, it was of interest to determine if any TAP alleles were associated with IDDM. In addition to the alleles of TAP1 that have been described, others were identified during this study. Diabetics and normal controls were screened for TAP1 using single-stranded conformational polymorphism and relative risk was determined. In the same population group we have studied extensively in the past, we found a higher association of a TAP1 allele with IDDM than with any single HLA-DP allele but the risk was lower than with HLA-DQB1*0302. These data provide new limits for IDDM susceptibility to the 190-kb interval between TAP1 and HLA-DQB1.
先前已经证明,具有某些DR等位基因的个体患胰岛素依赖型糖尿病(IDDM)的相对风险增加。与某些DQ等位基因的疾病关联更强,但与DP的关联很小,这为DQ和DP之间430 kb的疾病关联划定了界限。最近描述的TAP(与抗原加工相关的转运蛋白)基因已定位在DP和DQ之间大约中间位置。因此,确定是否有任何TAP等位基因与IDDM相关是很有意义的。除了已描述的TAP1等位基因外,在本研究中还鉴定出了其他等位基因。使用单链构象多态性对糖尿病患者和正常对照进行TAP1筛查,并确定相对风险。在我们过去广泛研究的同一人群组中,我们发现一个TAP1等位基因与IDDM的关联高于任何单个HLA-DP等位基因,但风险低于HLA-DQB1*0302。这些数据为IDDM易感性提供了新的界限,范围在TAP1和HLA-DQB1之间的190 kb区间。