甲基化
RNA甲基化
核糖核酸
细胞生物学
程序性细胞死亡
癌症研究
生物
化学
甲基转移酶
细胞凋亡
遗传学
基因
作者
Shuang Li,Xiangyu Deng,Deepak Pathak,Rashmi Basavaraj,Lina Sun,Yating Cheng,Jianrong Li,Marissa Burke,Gavin W. Britz,Chao Cheng,Yang Gao,Yi‐Lan Weng
标识
DOI:10.1101/2024.06.29.601251
摘要
Abstract m 6 A RNA methylation suppresses the immunostimulatory potential of endogenous RNA. Deficiency of m 6 A provokes inflammatory responses and cell death, but the underlying mechanisms remain elusive. Here we showed that the noncoding RNA 7SK gains immunostimulatory potential upon m 6 A depletion and subsequently activates the RIG-I/MAVS axis to spark interferon (IFN) signaling cascades. Concomitant excess of IFN and m 6 A deficiency synergistically facilitate the formation of RNA G-quadruplexes (rG4) to promote ZBP1-mediated necroptotic cell death. Collectively, our findings delineate a hitherto uncharacterized mechanism that links m 6 A dysregulation with ZBP1 activity in triggering inflammatory cell death.
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