Otabe S, Clement K, Dina C, Pelloux V, Guy-Grand B, Froguel P, Vasseur F
CNRS UPRESA 8090, Institute of Biology of Lille, CHRU Lille, France.
Diabetologia. 2000 Feb;43(2):245-9. doi: 10.1007/s001250050037.
AIMS/HYPOTHESIS: In obese French Caucasian subjects we previously described a silent UCP3 Tyr99Tyr mutation, associated with body mass index. We hypothesised that an unknown polymorphism in the vicinity of the gene could contribute to obesity.
Morbidly obese subjects were screened for mutations in 1 kb upstream from the UCP3 gene. Association studies were done between a variant and obesity in 401 morbidly obese and 231 control subjects.
We detected three rare genetic variants and one polymorphism: a +5 G-->A in exon 1, a -155 C-->T, a -439 A insertion and a -55 C-->T located 6 bp from the putative TATA box. This variant was in linkage disequilibrium with the Tyr99Tyr polymorphism. Frequencies of the variant allele at the -55 locus were similar in the obese and control groups (0.23 vs 0.21). The -55 polymorphism was associated with BMI in the obese group (p = 0.0031): BMI was higher in TT than in CC or CT patients. Likewise control subjects with a TT genotype had a higher BMI (p = 0.03). In the obese group, homozygosity for this variant is a risk factor for high BMI (odds ratio: 1:75, p = 0.02). Obese patients were divided into tertiles according to physical activity. In the group with a wild C/C genotype, BMI was negatively associated with physical activity (p = 0.015).
CONCLUSION/INTERPRETATION: The C-->T polymorphism in the 5' sequences of the UCP3 gene might contribute to the corpulence in obese and normal weight subjects and alter the benefit of physical activity. The UCP3 gene can be considered as a gene modifying corpulence.
目的/假设:在肥胖的法国白种人受试者中,我们之前描述了一种与体重指数相关的沉默型UCP3 Tyr99Tyr突变。我们推测该基因附近的一个未知多态性可能与肥胖有关。
对病态肥胖受试者进行UCP3基因上游1 kb区域的突变筛查。在401例病态肥胖受试者和231例对照受试者中进行了一个变异体与肥胖的关联研究。
我们检测到三个罕见的基因变异和一个多态性:外显子1中的+5 G→A、-155 C→T、-439 A插入以及位于假定TATA框6 bp处的-55 C→T。该变异体与Tyr99Tyr多态性处于连锁不平衡状态。肥胖组和对照组中-55位点变异等位基因的频率相似(分别为0.23和0.21)。肥胖组中-55多态性与体重指数相关(p = 0.0031):TT基因型患者的体重指数高于CC或CT基因型患者。同样,TT基因型的对照受试者体重指数也较高(p = 0.03)。在肥胖组中,该变异体的纯合性是高体重指数的一个危险因素(优势比:1:75,p = 0.02)。肥胖患者根据体力活动水平分为三分位数。在野生C/C基因型组中,体重指数与体力活动呈负相关(p = 0.015)。
结论/解读:UCP3基因5'序列中的C→T多态性可能导致肥胖和正常体重受试者肥胖,并改变体力活动的益处。UCP3基因可被视为一个影响肥胖的修饰基因。