Proceedings of the National Academy of Sciences · 2013 · 169 citations · 25 references
Life SciencesMolecular BiologyMolecular GeneticsMetabolic RegulationMetabolismSignal TransductionAdipose TissueAmino Acid MetabolismMetabolic SignalingNutrient SensingNutrient-gene RegulationNutrient-sensing PathwaysAmino Acid Sensing PathwaysAmino AcidsLoss-of-function MutationsMammalian Target Of Rapamycin SignalingMtor Complex 1 RegulationMtor Complex 1 SignalingMurine ModelsNutrient-regulated Signal Transduction
SNPs in the first intron of FTO (fat mass and obesity associated) are strongly associated with human obesity. While it is not yet formally established that this effect is mediated through the actions of the FTO protein itself, loss of function mutations in FTO or its murine homologue Fto result in severe growth retardation, and mice globally overexpressing FTO are obese. The mechanisms through which FTO influences growth and body composition are unknown. We describe a role for FTO in the coupling of amino acid levels to mammalian target of rapamycin complex 1 signaling. These findings suggest that FTO may influence body composition through playing a role in cellular nutrient sensing.
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