Author:
Li Shuang,Deng Xiangyu,Pathak Deepak,Basavaraj Rashmi,Sun Lina,Cheng Yating,Li Jian-Rong,Burke Marissa,Britz Gavin W.,Cheng Chao,Gao Yang,Weng Yi-Lan
Abstract
Abstractm6A RNA methylation suppresses the immunostimulatory potential of endogenous RNA. Deficiency of m6A provokes inflammatory responses and cell death, but the underlying mechanisms remain elusive. Here we showed that the noncoding RNA 7SK gains immunostimulatory potential upon m6A depletion and subsequently activates the RIG-I/MAVS axis to spark interferon (IFN) signaling cascades. Concomitant excess of IFN and m6A 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 m6A dysregulation with ZBP1 activity in triggering inflammatory cell death.
Publisher
Cold Spring Harbor Laboratory