4.6 Review

Where to go with FTO?

Journal

TRENDS IN ENDOCRINOLOGY AND METABOLISM
Volume 22, Issue 2, Pages 53-59

Publisher

ELSEVIER SCIENCE LONDON
DOI: 10.1016/j.tem.2010.11.001

Keywords

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Funding

  1. UK Medical Research Council Centre for Obesity and Related Metabolic Disorders (MRC-CORD)
  2. MRC [G09000554, ID 91140]
  3. EU [FP7-HEALTH-2009-241592 EuroCHIP]
  4. Medical Research Council [G0900554] Funding Source: researchfish
  5. MRC [G0900554] Funding Source: UKRI

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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.

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