脂肪生成
去甲基化
脱甲基酶
核糖核酸
N6-甲基腺苷
信使核糖核酸
甲基化
细胞生物学
抄写(语言学)
化学
生物化学
小RNA
表观遗传学
生物
DNA甲基化
分子生物学
甲基转移酶
基因表达
体外
基因
哲学
语言学
作者
Lina Wang,Chengli Song,Na Wang,Songyu Li,Qiaoling Liu,Zhen Sun,Kai Wang,Shi‐Cang Yu,Qingkai Yang
标识
DOI:10.1038/s41589-020-0601-2
摘要
Metabolism is often regulated by the transcription and translation of RNA. In turn, it is likely that some metabolites regulate enzymes controlling reversible RNA modification, such as N6-methyladenosine (m6A), to modulate RNA. This hypothesis is at least partially supported by the findings that multiple metabolic diseases are highly associated with fat mass and obesity-associated protein (FTO), an m6A demethylase. However, knowledge about whether and which metabolites directly regulate m6A remains elusive. Here, we show that NADP directly binds FTO, independently increases FTO activity, and promotes RNA m6A demethylation and adipogenesis. We screened a set of metabolites using a fluorescence quenching assay and NADP was identified to remarkably bind FTO. In vitro demethylation assays indicated that NADP enhances FTO activity. Furthermore, NADP regulated mRNA m6A via FTO in vivo, and deletion of FTO blocked NADP-enhanced adipogenesis in 3T3-L1 preadipocytes. These results build a direct link between metabolism and RNA m6A demethylation.
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