Obesity and FTO: Changing Focus at a Complex Locus

Cell Metab. 2014 Nov 4;20(5):710-718. doi: 10.1016/j.cmet.2014.09.010. Epub 2014 Oct 23.

Abstract

The fat mass and obesity-associated (FTO) gene was placed center stage when common intronic variants within the gene were robustly associated with human obesity. Murine models of perturbed Fto expression have shown effects on body weight and composition. However, a clear understanding of the link between FTO intronic variants and FTO activity has remained elusive. Two recent reports now indicate that obesity-associated SNPs appear functionally connected not with FTO but with two neighboring genes: IRX3 and RPGRIP1L. Here, we review these new findings and consider the implications for future analysis of GWAS hits.

Publication types

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

MeSH terms

  • Animals
  • Dopamine / metabolism
  • Genetic Loci*
  • Genome-Wide Association Study
  • Humans
  • Mixed Function Oxygenases / genetics*
  • Obesity / genetics*
  • Polymorphism, Single Nucleotide / genetics

Substances

  • Mixed Function Oxygenases
  • Dopamine