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烟酰胺腺嘌呤二核苷酸磷酸(NADP)通过增强脂肪量和肥胖相关蛋白(FTO)的活性来调节RNA N6-甲基腺嘌呤(mA)甲基化及脂肪生成。

NADP modulates RNA mA methylation and adipogenesis via enhancing FTO activity.

作者信息

Wang Lina, Song Chengli, Wang Na, Li Songyu, Liu Qiaoling, Sun Zhen, Wang Kai, Yu Shi-Cang, Yang Qingkai

机构信息

Institute of Cancer Stem Cell, DaLian Medical University, Dalian, Liaoning, China.

Department of Stem Cell and Regenerative Medicine, Southwest Hospital, Third Military Medical University (Army Medical University), Chongqing, China.

出版信息

Nat Chem Biol. 2020 Dec;16(12):1394-1402. doi: 10.1038/s41589-020-0601-2. Epub 2020 Jul 27.

Abstract

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 N-methyladenosine (mA), 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 mA demethylase. However, knowledge about whether and which metabolites directly regulate mA remains elusive. Here, we show that NADP directly binds FTO, independently increases FTO activity, and promotes RNA mA 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 mA 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 mA demethylation.

摘要

新陈代谢通常受RNA转录和翻译的调控。反过来,一些代谢物可能会调节控制可逆RNA修饰(如N-甲基腺苷(mA))的酶,从而调控RNA。这一假说至少部分得到了以下研究结果的支持:多种代谢性疾病与mA去甲基化酶——脂肪量和肥胖相关蛋白(FTO)高度相关。然而,关于代谢物是否以及哪些代谢物直接调控mA,目前仍不清楚。在这里,我们表明烟酰胺腺嘌呤二核苷酸磷酸(NADP)直接结合FTO,独立增加FTO活性,并促进RNA的mA去甲基化和脂肪生成。我们使用荧光猝灭测定法筛选了一组代谢物,发现NADP能与FTO显著结合。体外去甲基化测定表明,NADP增强了FTO活性。此外,NADP在体内通过FTO调节mRNA的mA,敲除FTO可阻断NADP增强的3T3-L1前脂肪细胞的脂肪生成。这些结果建立了新陈代谢与RNA的mA去甲基化之间的直接联系。

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