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The Obesity-Associated FTO Gene Encodes a 2-Oxoglutarate-Dependent Nucleic Acid Demethylase

机译:肥胖相关的FTO基因编码2-氧戊二酸依赖性核酸脱甲基酶

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摘要

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.
机译:FTO(肥胖和肥胖相关)基因的变异与人类体重指数增加有关。在这里,我们通过生物信息学分析表明FTO与Fe(II)和2-氧代戊二酸酯依赖性加氧酶共享序列基序。我们发现重组鼠Fto催化单链DNA中3-甲基胸腺嘧啶的Fe(II)-和2OG依赖性脱甲基化,同时产生琥珀酸盐,甲醛和二氧化碳。与在核酸去甲基化中的潜在作用一致,Fto定位于转染细胞中的核。对野生型小鼠的研究表明,Fto信使RNA(mRNA)在大脑中含量最高,尤其是在下丘脑核中控制能量平衡,并且弓形核中的Fto mRNA水平受进食和禁食的调节。现在,研究可以直接用于确定生理相关的FTO底物,以及核酸甲基化状态如何与增加的脂肪量相关联。

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