The biology of FTO: from nucleic acid demethylase to amino acid sensor

被引:39
|
作者
Gulati, Pawan [1 ,2 ]
Yeo, Giles S. H. [1 ,2 ]
机构
[1] Univ Cambridge, MRC Metab Dis Unit, Wellcome Trust MRC Inst Metab Sci, Addenbrookes Hosp,Metab Res Labs, Cambridge CB2 0QQ, England
[2] Addenbrookes Hosp, NIHR Cambridge Biomed Res Ctr, Cambridge, England
基金
英国医学研究理事会;
关键词
Demethylation; Food intake; Genetics; Growth; GWAS; mTOR; Nutrients; Obesity; Review; Translation; BODY-MASS INDEX; TRANSFER-RNA SYNTHETASES; EARLY-ONSET OBESITY; ENERGY-INTAKE; FOOD-INTAKE; GENETIC-VARIANTS; FAT MASS; WAIST CIRCUMFERENCE; FRAMESHIFT MUTATION; NEUROTROPHIC FACTOR;
D O I
10.1007/s00125-013-2999-5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Genome-wide association studies have revealed that single-nucleotide polymorphisms in the first intron of the gene encoding fat mass and obesity-associated protein (FTO) are robustly associated with BMI and obesity. Subsequently, this association with body weight, which is replicable across multiple populations and different age groups, has been unequivocally linked to increased food intake. Although evidence from a number of animal models with perturbed FTO expression indicates a role for FTO in energy homeostasis, to date, no conclusive link has been made between the risk alleles and FTO expression or its physiological role. FTO is a nucleic acid demethylase, and a deficiency in FTO leads to a complex phenotype highlighted by postnatal growth retardation, pointing to some fundamental developmental role. Recent emerging data now points to a role for FTO in the sensing of nutrients and the regulation of translation and growth. In this review, we explore the in vivo and in vitro evidence detailing the complex biology of FTO and discuss how these might link to the regulation of body weight.
引用
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页码:2113 / 2121
页数:9
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