| Literature DB >> 12559634 |
Masataka Nishimura1, Hiroshi Obayashi, Ikuko Mizuta, Hirokazu Hara, Tetsuo Adachi, Mitsuhiro Ohta, Hisataka Tegoshi, Michiaki Fukui, Goji Hasegawa, Hirofumi Shigeta, Yoshihiro Kitagawa, Koji Nakano, Ryuji Kaji, Naoto Nakamura.
Abstract
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.Entities:
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Year: 2003 PMID: 12559634 DOI: 10.1016/s0198-8859(02)00799-1
Source DB: PubMed Journal: Hum Immunol ISSN: 0198-8859 Impact factor: 2.850