The Obesity-Associated <i>FTO</i> Gene Encodes a 2-Oxoglutarate-Dependent Nucleic Acid Demethylase

Thomas Gerken(Mansfield University), Christophe A. Girard(Mansfield University), Yi‐Chun Loraine Tung(Mansfield University), Celia J. Webby(Mansfield University), Vladimı́r Saudek(Mansfield University), Kirsty S. Hewitson(Mansfield University), Giles S.H. Yeo(Mansfield University), M.A. McDonough(Mansfield University), Sharon L. Cunliffe(Mansfield University), Luke A. McNeill(Mansfield University), Juris Galvanovskis(Mansfield University), Patrik Rorsman(Mansfield University), Peter Robins(Mansfield University), Xavier Prieur(Mansfield University), Anthony P. Coll(Mansfield University), Marcella Ma(Mansfield University), Z Jovanović(Mansfield University), I. Sadaf Farooqi(Mansfield University), Barbara Sedgwick(Mansfield University), Inês Barroso(Mansfield University), Tomas Lindahl(Mansfield University), Chris P. Ponting(Mansfield University), Frances M. Ashcroft(Mansfield University), Stephen O’Rahilly(Mansfield University), Christopher J. Schofield(Mansfield University)
Science
November 8, 2007
Cited by 1,522Open Access
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Abstract

Variants in the FTO (fat mass and obesity associated) gene are associated with increased body mass index in humans. Here, we show by bioinformatics analysis that FTO shares sequence motifs with Fe(II)- and 2-oxoglutarate-dependent oxygenases. We find that recombinant murine Fto catalyzes the Fe(II)- and 2OG-dependent demethylation of 3-methylthymine in single-stranded DNA, with concomitant production of succinate, formaldehyde, and carbon dioxide. Consistent with a potential role in nucleic acid demethylation, Fto localizes to the nucleus in transfected cells. Studies of wild-type mice indicate that Fto messenger RNA (mRNA) is most abundant in the brain, particularly in hypothalamic nuclei governing energy balance, and that Fto mRNA levels in the arcuate nucleus are regulated by feeding and fasting. Studies can now be directed toward determining the physiologically relevant FTO substrate and how nucleic acid methylation status is linked to increased fat mass.


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