Han ZF, Niu TH, Chang JB, Lei XG, Zhao MY, Wang Q, Cheng W, Wang JJ, Feng Y, Chai JJ. Crystal structure of the FTO protein reveals basis for its substrate specificity. NATURE 464 (7292): 1103 - 1238 1205-1210, 2010

Abstract Recent studies have unequivocally associated the fat mass and obesity-associated (FTO) gene with the risk of obesity. In vitro FTO protein is an AlkB-like DNA/RNA demethylase with a strong preference for 3-methylthymidine (3-meT) in single-stranded DNA or 3-methyluracil (3-meU) in single-stranded RNA. Here we report the crystal structure of FTO in complex with the mononucleotide 3-meT. FTO comprises an amino-terminal AlkB-like domain and a carboxy-terminal domain with a novel fold. Biochemical assays show that these two domains interact with each other, which is required for FTO catalytic activity. In contrast with the structures of other AlkB members, FTO possesses an extra loop covering one side of the conserved jelly-roll motif. Structural comparison shows that this loop selec......