Nishimura Masataka, Obayashi Hiroshi, Mizuta Ikuko, Hara Hirokazu, Adachi Tetsuo, Ohta Mitsuhiro, Tegoshi Hisataka, Fukui Michiaki, Hasegawa Goji, Shigeta Hirofumi, Kitagawa Yoshihiro, Nakano Koji, Kaji Ryuji, Nakamura Naoto
Department of the Clinical Neuroscience, Tokushima University Hospital, Japan.
Hum Immunol. 2003 Feb;64(2):302-9. doi: 10.1016/s0198-8859(02)00799-1.
The human leukocyte antigen (HLA) class III region, located on chromosome 6p21, has been regarded as one of the susceptible loci for type 1 diabetes. Because it contains many genes related to inflammatory and immune responses, including tumor necrosis factor (TNF), lymphotoxin-alpha (LT-alpha), and allograft inflammatory factor 1 (AIF-1) genes, it is unclear which gene within the class III region is responsible for the susceptibility to the disease. We sequenced the AIF-1 gene region and detected three novel polymorphisms, all of which were diallelic and localized at introns. Then, we investigated AIF-1, TNF, and LT-alpha gene polymorphisms in 165 patients with type 1 diabetes, consisting of 90 patients with young-onset type 1 diabetes, 75 patients with adult-onset type 1 diabetes, and 200 control patients. We also analyzed TNF receptors type 1 (TNFR1) and type 2 (TNFR2) gene polymorphisms, located on chromosome 12p13 and 1p36, respectively. Although there were significant differences between type 1 diabetes patients and controls in the distributions of TNF promoter polymorphisms at position -1031 and -857, and LT-alpha gene NcoI polymorphism, none of them was independently associated with the disease after two-locus analysis with HLA class II alleles. We detected the significantly increased frequency of the -383C allele, located in the TNFR-1 promoter region, in both young-onset and adult-onset diabetes patients compared with controls. In addition, the -383C allele was found to be associated with higher expression of the TNFR1 gene than that of -383A allele in in vitro expression. These results suggest that the TNFR1 gene region might be a susceptible locus to type 1 diabetes in Japanese.
人类白细胞抗原(HLA)Ⅲ类区域位于6号染色体p21上,一直被视为1型糖尿病的易感基因座之一。由于该区域包含许多与炎症和免疫反应相关的基因,包括肿瘤坏死因子(TNF)、淋巴毒素-α(LT-α)和移植炎症因子1(AIF-1)基因,因此尚不清楚Ⅲ类区域内的哪个基因导致了该疾病的易感性。我们对AIF-1基因区域进行了测序,检测到三个新的多态性,均为双等位基因且位于内含子中。然后,我们调查了165例1型糖尿病患者(包括90例早发型1型糖尿病患者、75例成人型1型糖尿病患者)和200例对照患者的AIF-1、TNF和LT-α基因多态性。我们还分析了分别位于12号染色体p13和1号染色体p36上的肿瘤坏死因子受体1型(TNFR1)和2型(TNFR₂)基因多态性。虽然1型糖尿病患者与对照在TNF启动子-1031和-857位点多态性以及LT-α基因NcoI多态性的分布上存在显著差异,但在与HLAⅡ类等位基因进行两位点分析后,这些差异均与疾病无独立相关性。我们检测到,与对照相比,早发型和成人型糖尿病患者中位于TNFR-1启动子区域的-383C等位基因频率显著增加。此外,在体外表达中发现-383C等位基因与TNFR1基因的表达高于-383A等位基因相关。这些结果表明,TNFR1基因区域可能是日本人1型糖尿病的一个易感基因座。