NADP modulates RNA m6A methylation and adipogenesis via enhancing FTO activity

被引:99
作者
Wang, Lina [1 ]
Song, Chengli [1 ]
Wang, Na [1 ]
Li, Songyu [1 ]
Liu, Qiaoling [1 ]
Sun, Zhen [1 ]
Wang, Kai [1 ]
Yu, Shi-Cang [2 ]
Yang, Qingkai [1 ]
机构
[1] DaLian Med Univ, Inst Canc Stem Cell, Dalian, Liaoning, Peoples R China
[2] Third Mil Med Univ, Army Med Univ, Southwest Hosp, Dept Stem Cell & Regenerat Med, Chongqing, Peoples R China
基金
中国国家自然科学基金;
关键词
GENOME-WIDE ASSOCIATION; METABOLISM; INHIBITION; N-6-METHYLADENOSINE; PROLIFERATION; DEMETHYLATION; INACTIVATION; SUBSTRATE; PROTECTS; PATHWAY;
D O I
10.1038/s41589-020-0601-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
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 asN(6)-methyladenosine (m(6)A), 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 m(6)A demethylase. However, knowledge about whether and which metabolites directly regulate m(6)A remains elusive. Here, we show that NADP directly binds FTO, independently increases FTO activity, and promotes RNA m(6)A 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 m(6)A 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 m(6)A demethylation.
引用
收藏
页码:1394 / +
页数:29
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