去甲基化
核酸
FTO基因
化学
信使核糖核酸
DNA去甲基化
核糖核酸
生物化学
脱甲基酶
基因
分子生物学
基因表达
生物
表观遗传学
DNA甲基化
基因型
单核苷酸多态性
作者
Thomas Gerken,Christophe A. Girard,Yi‐Chun 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
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2007-11-08
卷期号:318 (5855): 1469-1472
被引量:1496
标识
DOI:10.1126/science.1151710
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.
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