Metabolic Disease Group, Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridgeshire, CB10 1SA, UK.
Trends Genet. 2010 Jun;26(6):266-74. doi: 10.1016/j.tig.2010.02.006. Epub 2010 Apr 8.
In 2007, an association of single nucleotide polymorphisms (SNPs) in the fat mass and obesity-associated (FTO) gene region with body mass index (BMI) and risk of obesity was identified in multiple populations, making FTO the first locus unequivocally associated with adiposity. At the time, FTO was a gene of unknown function and it was not known whether these SNPs exerted their effect on adiposity by affecting FTO or neighboring genes. Therefore, this breakthrough association inspired a wealth of in silico, in vitro, and in vivo analyses in model organisms and humans to improve knowledge of FTO function. These studies suggested that FTO plays a role in controlling feeding behavior and energy expenditure. Here, we review the approaches taken that provide a blueprint for the study of other obesity-associated genes in the hope that this strategy will result in increased understanding of the biological mechanisms underlying body weight regulation.
2007 年,在多个人群中发现了脂肪量和肥胖相关(FTO)基因区域中单核苷酸多态性(SNP)与体重指数(BMI)和肥胖风险之间的关联,这使得 FTO 成为第一个明确与肥胖相关的基因。当时,FTO 是一个功能未知的基因,并且尚不清楚这些 SNP 是否通过影响 FTO 或邻近基因来对肥胖产生影响。因此,这一突破性的关联激发了大量在模式生物和人类中进行的计算机模拟、体外和体内分析,以提高对 FTO 功能的认识。这些研究表明,FTO 在控制摄食行为和能量消耗方面发挥作用。在这里,我们回顾了所采用的方法,为研究其他肥胖相关基因提供了蓝图,希望这一策略将导致对体重调节背后的生物学机制的理解的增加。