N⁶-methyladenosine RNA modification suppresses antiviral innate sensing pathways via reshaping double-stranded RNA.

ABSTRACT: Double-stranded RNA (dsRNA) is a virus-encoded signature capable of triggering intracellular Rig-like receptors (RLR) to activate antiviral signaling, but whether intercellular dsRNA structural reshaping mediated by the N⁶-methyladenosine (m⁶A) modification modulates this process remains largely unknown. Here, we show that, in response to infection by the RNA virus Vesicular Stomatitis Virus (VSV), the m⁶A methyltransferase METTL3 translocates into the cytoplasm to increase m⁶A modification on virus-derived transcripts and decrease viral dsRNA formation, thereby reducing virus-sensing efficacy by RLRs such as RIG-I and MDA5 and dampening antiviral immune signaling. Meanwhile, the genetic ablation of METTL3 in monocyte or hepatocyte causes enhanced type I IFN expression and accelerates VSV clearance. Our findings thus implicate METTL3-mediated m⁶A RNA modification on viral RNAs as a negative regulator for innate sensing pathways of dsRNA, and also hint METTL3 as a potential therapeutic target for the modulation of anti-viral immunity.

SUBMITTER: Qiu W 

PROVIDER: S-EPMC7952553 | biostudies-literature | 2021 Mar

REPOSITORIES: biostudies-literature