Where to go with FTO?

Trends Endocrinol Metab. 2011 Feb;22(2):53-9. doi: 10.1016/j.tem.2010.11.001. Epub 2010 Dec 4.

Abstract

An understanding of the mechanisms underlying body-weight regulation is crucial to tackle the growing problem of obesity. Recent technological advances in the analysis of genetic variation have given novel insights into the molecular basis of common disease. In particular, genomic variants in the fat mass and obesity-associated (FTO) gene have been consistently associated with human adiposity and metabolic disorders. Studies of the product of this previously mysterious gene have formed a vanguard in the quest to turn statistical association into hard biology. In this review, we examine data from human genetic and murine studies that explore the potential role of FTO, a member of the Fe(II)- and 2-oxoglutarate-dependent oxygenase superfamily, in the regulation of energy homeostasis and metabolism.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Alpha-Ketoglutarate-Dependent Dioxygenase FTO
  • Animals
  • Body Mass Index
  • DNA Methylation
  • Energy Intake
  • Energy Metabolism / genetics
  • Genetic Predisposition to Disease
  • Homeostasis / genetics
  • Humans
  • Mice
  • Mutation
  • Obesity / genetics*
  • Phenotype
  • Polymorphism, Single Nucleotide / genetics
  • Proteins / chemistry
  • Proteins / genetics*
  • Proteins / physiology

Substances

  • Proteins
  • Alpha-Ketoglutarate-Dependent Dioxygenase FTO
  • FTO protein, human