MRC Harwell, Metabolism and Inflammation, Harwell Science and Innovation Campus, Harwell, UK.
Nat Genet. 2010 Dec;42(12):1086-92. doi: 10.1038/ng.713. Epub 2010 Nov 14.
Genome-wide association studies have identified SNPs within FTO, the human fat mass and obesity-associated gene, that are strongly associated with obesity. Individuals homozygous for the at-risk rs9939609 A allele weigh, on average, ~3 kg more than individuals with the low-risk T allele. Mice that lack FTO function and/or Fto expression display increased energy expenditure and a lean phenotype. We show here that ubiquitous overexpression of Fto leads to a dose-dependent increase in body and fat mass, irrespective of whether mice are fed a standard or a high-fat diet. Our results suggest that increased body mass results primarily from increased food intake. Mice with increased Fto expression on a high-fat diet develop glucose intolerance. This study provides the first direct evidence that increased Fto expression causes obesity in mice.
全基因组关联研究已经确定了 FTO 基因(人类脂肪量和肥胖相关基因)内与肥胖强烈相关的 SNPs。携带风险 rs9939609 A 等位基因的纯合子个体的体重比携带低风险 T 等位基因的个体平均重约 3 公斤。缺乏 FTO 功能和/或 Fto 表达的小鼠表现出增加的能量消耗和瘦表型。我们在这里表明,Fto 的普遍过表达导致体重和脂肪量的剂量依赖性增加,无论小鼠是喂食标准饮食还是高脂肪饮食。我们的结果表明,体重增加主要是由于食物摄入量增加所致。在高脂肪饮食下表达增加的 Fto 的小鼠会发展为葡萄糖不耐受。这项研究首次提供了直接证据,表明增加的 Fto 表达导致了肥胖。