Shiri-Sverdlov Ronit, Custers Anne, van Vliet-Ostaptchouk Jana V, van Gorp Patrick J J, Lindsey Patrick J, van Tilburg Jonathan H O, Zhernakova Sasha, Feskens Edith J M, van der A Daphne L, Dollé Martijn E T, van Haeften Timon W, Koeleman Bobby P C, Hofker Marten H, Wijmenga Cisca
Department of Molecular Genetics, Maastricht University, the Netherlands.
Diabetes. 2006 Feb;55(2):385-9. doi: 10.2337/diabetes.55.02.06.db05-0997.
Previously, we identified a locus on 11p influencing obesity in families with type 2 diabetes. Based on mouse studies, we selected TUB as a functional candidate gene and performed association studies to determine whether this controls obesity. We analyzed the genotypes of 13 single nucleotide polymorphisms (SNPs) around TUB in 492 unrelated type 2 diabetic patients with known BMI values. One SNP (rs1528133) was found to have a significant effect on BMI (1.54 kg/m(2), P = 0.006). This association was confirmed in a population enriched for type 2 diabetes, using 750 individuals who were not selected for type 2 diabetes. Two SNPs in linkage disequilibrium with rs1528133 and mapping to the 3' end of TUB, rs2272382, and rs2272383 also affected BMI by 1.3 kg/m2 (P = 0.016 and P = 0.010, respectively). Combined analysis confirmed this association (P = 0.005 and P = 0.002, respectively). Moreover, comparing 349 obese subjects (BMI >30 kg/m(2)) from the combined cohort with 289 normal subjects (BMI <25 kg/m(2)) revealed that the protective alleles have a lower frequency in obese subjects (odds ratio 1.32 [95% CI 1.04-1.67], P = 0.022). Altogether, data from the tubby mouse as well as these data suggest that TUB could be an important factor in controlling the central regulation of body weight in humans.
此前,我们在2型糖尿病家族中确定了11号染色体短臂上的一个影响肥胖的基因座。基于小鼠研究,我们选择TUB作为一个功能候选基因,并进行了关联研究,以确定其是否控制肥胖。我们分析了492名已知BMI值的非亲缘关系2型糖尿病患者中TUB周围13个单核苷酸多态性(SNP)的基因型。发现一个SNP(rs1528133)对BMI有显著影响(1.54kg/m²,P=0.006)。在一个未选择2型糖尿病的750人队列中,该关联在一个富含2型糖尿病的人群中得到了证实。与rs1528133处于连锁不平衡且定位于TUB 3'端的两个SNP,rs2272382和rs2272383也使BMI分别增加了1.3kg/m²(P分别为0.016和0.010)。联合分析证实了这种关联(P分别为0.005和0.002)。此外,将合并队列中的349名肥胖受试者(BMI>30kg/m²)与289名正常受试者(BMI<25kg/m²)进行比较,发现保护等位基因在肥胖受试者中的频率较低(优势比1.