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韩国人群中肿瘤坏死因子基因多态性的频率。

Frequencies of the tumor necrosis factor gene polymorphisms in the Korean population.

作者信息

Um Jae-Young, Kim Hyung-Min

机构信息

Department of Pharmacology, College of Oriental Medicine, Kyung Hee University, Seoul, South Korea.

出版信息

Hereditas. 2003;139(3):184-8. doi: 10.1111/j.1601-5223.2003.01741.x.

Abstract

Tumor necrosis factor (TNF), a potent immuno-modulator and pro-inflammatory cytokine, has been implicated in many pathological processes. The TNFA and the TNFB genes, which encode TNFalpha and TNFbeta, respectively, are both located on the short arm of chromosome 6 between the class I and class II regions of the HLA complex. A striking feature of the entire HLA complex is a high degree of genetic variation. Two biallelic polymorphisms in the TNFA (- 308G/A) and TNFB (+ 252A/G) genes have been reported to be associated with TNF production and with susceptibility to inflammatory diseases. Population information on polymorphisms is essential for the study of genetic diseases. The aim of this study is to obtain accurate information about polymorphisms in the TNF genes in the Korean population. Allele frequencies of TNFA (- 308G/A) and TNFB (+ 252A/G) were measured in 581 unrelated Korean individuals by PCR-RFLP. Allele frequencies of each polymorphism were determined and compared with those previously reported in other populations. A significant difference was found for the allele frequencies of TNFA and TNFB gene in Koreans compared with Europeans. The - 308/A allele in the TNFA gene was very rare in Asians (0.008-0.096). The frequency of the - 308/A allele in Koreans was considerably lower than in Europeans (0.120-0.189). Contrary to lower frequency of the -308/A allele, that of + 252/G allele in the TNFB gene was higher than in Koreans (0.445) compared with Europeans (0.29-0.39). The polymorphisms and allele frequencies obtained in this study will be useful for genetic studies of common inflammatory diseases.

摘要

肿瘤坏死因子(TNF)是一种强效免疫调节剂和促炎细胞因子,与许多病理过程有关。分别编码TNFα和TNFβ的TNFA和TNFB基因均位于6号染色体短臂上,在HLA复合体的I类和II类区域之间。整个HLA复合体的一个显著特征是高度的遗传变异。据报道,TNFA基因(-308G/A)和TNFB基因(+252A/G)中的两个双等位基因多态性与TNF产生以及炎症性疾病易感性相关。多态性的群体信息对于遗传疾病研究至关重要。本研究的目的是获取韩国人群中TNF基因多态性的准确信息。通过PCR-RFLP对581名无亲缘关系的韩国个体测量了TNFA基因(-308G/A)和TNFB基因(+252A/G)的等位基因频率。确定了每种多态性的等位基因频率,并与先前在其他群体中报道的频率进行比较。发现韩国人TNFA和TNFB基因的等位基因频率与欧洲人有显著差异。TNFA基因中的-308/A等位基因在亚洲人中非常罕见(0.008 - 0.096)。韩国人中-308/A等位基因的频率明显低于欧洲人(0.120 - 0.189)。与-308/A等位基因较低频率相反,TNFB基因中+252/G等位基因的频率在韩国人(0.445)中高于欧洲人(0.29 - 0.39)。本研究中获得的多态性和等位基因频率将有助于常见炎症性疾病的遗传研究。

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