The Obesity-AssociatedFTOGene Encodes a 2-Oxoglutarate-Dependent Nucleic Acid Demethylase
Author(s) -
Thomas Gerken,
Christophe A. Girard,
YiChun Loraine Tung,
Celia J. Webby,
Vladimı́r Saudek,
Kirsty S. Hewitson,
Giles S.H. Yeo,
M.A. McDonough,
Sharon L. Cunliffe,
Luke A. McNeill,
Juris Galvanovskis,
Patrik Rorsman,
Peter Robins,
Xavier Prieur,
Anthony P. Coll,
Marcella Ma,
Z Jovanović,
I. Sadaf Farooqi,
Barbara Sedgwick,
Inês Barroso,
Tomas Lindahl,
Chris P. Ponting,
Frances M. Ashcroft,
Stephen O’Rahilly,
Christopher J. Schofield
Publication year - 2007
Publication title -
science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.1151710
Subject(s) - demethylation , nucleic acid , fto gene , chemistry , messenger rna , dna demethylation , rna , biochemistry , demethylase , gene , microbiology and biotechnology , gene expression , biology , epigenetics , dna methylation , genotype , single nucleotide polymorphism
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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