Department of Molecular and Genetic Epidemiology, Faculty of Medicine, University of Tsukuba, Tsukuba, Ibaraki, Japan.
Int J Obes (Lond). 2013 Sep;37(9):1204-10. doi: 10.1038/ijo.2012.206. Epub 2012 Dec 11.
Obesity is a growing health concern in the Oceanic populations. To investigate the genetic factors associated with adult obesity in the Oceanic populations, the association of single nucleotide polymorphisms (SNPs) of the beta-2 adrenergic receptor (ADRB2) gene with obesity was examined in 694 adults living in Tonga and Solomon Islands.
A screening for variation in 16 Oceanic subjects detected 17 SNPs in the entire region of ADRB2, of which nine SNPs including two non-synonymous ones, rs1042713 (Arg16Gly) and rs1042714 (Gln27Glu), were further genotyped for all subjects. The rs34623097-A allele, at a SNP located upstream of ADRB2, showed the strongest association with risk for obesity in a logistic regression analysis adjusted for age, sex, and population (P=5.6 × 10(-4), odds ratio [OR]=2.5, 95% confidence interval [CI]=1.5-4.2). The 27Glu was also significantly associated with obesity in the single-point association analysis (P=0.013, OR=2.0, 95%CI=1.2-3.4); however, this association was no longer significant after adjustment for rs34623097 since these SNPs were in linkage disequilibrium with each other. A copy of the obesity-risk allele, rs34623097-A, led to a 1.6 kg/m(2) increase in body mass index (BMI; defined as weight in kilograms divided by height in meters squared) (P=0.0019). A luciferase reporter assay indicated that rs34623097-A reduced the transcriptional activity of the luciferase reporter gene by approximately 10% compared with rs34623097-G. An electrophoretic mobility shift assay demonstrated that rs34623097 modulated the binding affinity with nuclear factors. An evolutionary analysis implies that a G>A mutation at rs34623097 occurred in the Neandertal genome and then the rs34623097-A allele flowed into the ancestors of present-day humans.
The present results suggest that rs34623097-A, which would lead to lower expression of ADRB2, contributes to the onset of obesity in the Oceanic populations.
肥胖是大洋洲人群日益严重的健康问题。为了研究与成年肥胖相关的遗传因素,我们在居住在汤加和所罗门群岛的 694 名成年人中研究了β-2 肾上腺素能受体(ADRB2)基因的单核苷酸多态性(SNP)与肥胖之间的关联。
对 16 名大洋洲个体的变异进行筛查,在 ADRB2 的整个区域发现了 17 个 SNP,其中包括两个非同义 SNP,rs1042713(Arg16Gly)和 rs1042714(Gln27Glu),对所有受试者进一步进行了基因分型。位于 ADRB2 上游的 SNP rs34623097-A 等位基因在调整年龄、性别和人群的逻辑回归分析中与肥胖风险最强相关(P=5.6×10(-4),优势比[OR]=2.5,95%置信区间[CI]=1.5-4.2)。单点关联分析也表明 27Glu 与肥胖显著相关(P=0.013,OR=2.0,95%CI=1.2-3.4);然而,由于这些 SNP 之间存在连锁不平衡,在调整 rs34623097 后,这种关联不再显著。肥胖风险等位基因 rs34623097-A 的一个拷贝导致体重指数(BMI;定义为体重以千克为单位除以身高以米为单位)增加 1.6kg/m(2)(P=0.0019)。荧光素酶报告基因检测表明,与 rs34623097-G 相比,rs34623097-A 降低了荧光素酶报告基因的转录活性约 10%。电泳迁移率变动分析表明,rs34623097 调节了与核因子的结合亲和力。进化分析表明,rs34623097 处的 G>A 突变发生在尼安德特人基因组中,然后 rs34623097-A 等位基因流入了当今人类的祖先。
本研究结果表明,导致 ADRB2 表达降低的 rs34623097-A 等位基因可能导致大洋洲人群肥胖的发生。