Overexpression of Fto leads to increased food intake and results in obesity

Nat Genet. 2010 Dec;42(12):1086-92. doi: 10.1038/ng.713. Epub 2010 Nov 14.

Abstract

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adiposity / drug effects
  • Adiposity / genetics
  • Alpha-Ketoglutarate-Dependent Dioxygenase FTO
  • Animals
  • Area Under Curve
  • Body Temperature
  • Circadian Rhythm / drug effects
  • Circadian Rhythm / genetics
  • Dietary Fats / administration & dosage
  • Dietary Fats / pharmacology
  • Energy Metabolism / drug effects
  • Energy Metabolism / genetics
  • Feeding Behavior / drug effects
  • Feeding Behavior / physiology*
  • Female
  • Glucose / metabolism
  • Glucose Tolerance Test
  • Homeostasis / genetics
  • Male
  • Mice
  • Mixed Function Oxygenases
  • Models, Animal
  • Motor Activity / drug effects
  • Obesity / blood
  • Obesity / genetics*
  • Oxo-Acid-Lyases / genetics
  • Oxo-Acid-Lyases / metabolism*

Substances

  • Dietary Fats
  • Mixed Function Oxygenases
  • FTO protein, mouse
  • Alpha-Ketoglutarate-Dependent Dioxygenase FTO
  • Oxo-Acid-Lyases
  • Glucose