Tseng L H, Chen P J, Lin M T, Shau W Y, Chaung S M, Martin P J, Hansen J A
Department of Medical Genetics, Pathology and Oncology, National Taiwan University Hospital, and Graduate Institutes of Clinical Medicine and Cancer Research Center, National Taiwan University, Taipei, Taiwan.
Tissue Antigens. 2001 Apr;57(4):318-24. doi: 10.1034/j.1399-0039.2001.057004318.x.
Previous studies have suggested that a variable number tandem repeat (VNTR) polymorphism in the second intron of the interleukin-1 receptor antagonist (IL-1Ra) gene and the single nucleotide polymorphisms at positions -511 and +3954 of the IL-1beta gene might be associated with increased risks of chronic inflammatory diseases, autoimmune diseases and gastric cancer. In the present study, IL-1beta and IL-1Ra genotypes were analyzed among Asians in Taiwan and Caucasians in North America. We identified a novel polymorphism with 3 nucleotide substitutions in the IL-1Ra VNTR 2-repeat allele. One of the substitutions corresponds with the fourth 3' end nucleotide of the reverse primer that is often used for analysis of the IL-1Ra-associated VNTR locus. Mismatching between this primer and the 2-repeat allele can cause misleading amplification results when stringent conditions are used for annealing. The estimated haplotype frequencies of the variant IL-1 genes were significantly different between Taiwanese and Caucasians. The frequency of the pro-inflammatory IL-1Ra 2-repeat allele was significantly lower in Taiwanese than in Caucasians. In contrast, the frequencies of the pro-inflammatory IL-1beta -511T allele and +3954C allele were significantly higher among Taiwanese compared with Caucasians.
先前的研究表明,白细胞介素-1受体拮抗剂(IL-1Ra)基因第二内含子中的可变数目串联重复序列(VNTR)多态性以及IL-1β基因-511和+3954位置的单核苷酸多态性可能与慢性炎症性疾病、自身免疫性疾病和胃癌风险增加有关。在本研究中,对台湾的亚洲人和北美的白种人的IL-1β和IL-1Ra基因型进行了分析。我们在IL-1Ra VNTR 2重复等位基因中鉴定出一种具有3个核苷酸替换的新型多态性。其中一个替换与常用于分析IL-1Ra相关VNTR位点的反向引物的第四个3'末端核苷酸相对应。当使用严格条件进行退火时,该引物与2重复等位基因之间的错配会导致误导性的扩增结果。台湾人和白种人之间变异IL-1基因的估计单倍型频率存在显著差异。促炎IL-1Ra 2重复等位基因的频率在台湾人中显著低于白种人。相反,与白种人相比,台湾人中促炎IL-1β -511T等位基因和+3954C等位基因的频率显著更高。