Norman R A, Bogardus C, Ravussin E
Clinical Diabetes and Nutrition Section, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Phoenix, Arizona 85016, USA.
J Clin Invest. 1995 Jul;96(1):158-62. doi: 10.1172/JCI118016.
Because tumor necrosis factor-alpha (TNF-alpha) expression is increased in adipose tissue of both rodent models of obesity and obese humans, it has been considered as a candidate gene for obesity. Pima Indians were scored for genotypes at three polymorphic dinucleotide repeat loci (markers) near the gene TNF-alpha at 6p21.3. In a sib-pair linkage analysis, percent body fat, as measured by hydrostatic weighing, was linked (304 sib-pairs, P = 0.002) to the marker closest (10 kb) to TNF-alpha. The same marker was associated (P = 0.01) by analysis of variance with BMI. To search for possible DNA variants in TNF-alpha that contribute to obesity, single stranded conformational polymorphism analysis was performed from 20 obese and 20 lean subjects. Primer pairs were designed for the entire TNF-alpha protein coding region and part of the promoter. Only a single polymorphism located in the promoter region was detected. No association could be demonstrated between alleles at this polymorphism and percent body fat. We conclude that the linkage of TNF-alpha to obesity might be due to a sequence variant undetected in TNF-alpha or due to a variant in some other closely linked gene.
由于在肥胖啮齿动物模型和肥胖人类的脂肪组织中肿瘤坏死因子-α(TNF-α)表达均增加,它已被视为肥胖的候选基因。对皮马印第安人在位于6p21.3的TNF-α基因附近的三个多态性二核苷酸重复位点(标记)的基因型进行了评分。在同胞对连锁分析中,通过水下称重测量的体脂百分比与距离TNF-α最近(10 kb)的标记相关联(304对同胞,P = 0.002)。通过方差分析,同一标记与BMI相关(P = 0.01)。为了寻找TNF-α中可能导致肥胖的DNA变异,对20名肥胖和20名瘦受试者进行了单链构象多态性分析。针对整个TNF-α蛋白编码区和部分启动子设计了引物对。仅在启动子区域检测到一个多态性。该多态性的等位基因与体脂百分比之间未显示出关联。我们得出结论,TNF-α与肥胖的连锁可能是由于TNF-α中未检测到的序列变异或其他一些紧密连锁基因中的变异所致。