PKACs attenuate innate antiviral response by phosphorylating VISA and priming it for MARCH5-mediated degradation.
Sensing of viral RNA by RIG-I-like receptors initiates innate antiviral response, which is mediated by the central adaptor VISA. How the RIG-I-VISA-mediated antiviral response is terminated at the late phase of infection is enigmatic. Here we identified the protein kinase A catalytic (PKAC) subunits α and β as negative regulators ... of RNA virus-triggered signaling in a redundant manner. Viral infection up-regulated cellular cAMP levels and activated PKACs, which then phosphorylated VISA at T54. This phosphorylation abrogated virus-induced aggregation of VISA and primed it for K48-linked polyubiquitination and degradation by the E3 ligase MARCH5, leading to attenuation of virus-triggered induction of downstream antiviral genes. PKACs-deficiency or inactivation by the inhibitor H89 potentiated innate immunity to RNA viruses in cells and mice. Our findings reveal a critical mechanism of attenuating innate immune response to avoid host damage at the late phase of viral infection by the house-keeping PKA kinase.
Mesh Terms:
Adaptor Proteins, Signal Transducing, Animals, Cyclic AMP-Dependent Protein Kinase Catalytic Subunits, HEK293 Cells, Humans, Immunity, Innate, Immunoblotting, Immunoprecipitation, Membrane Proteins, Mice, Phosphorylation, Respirovirus Infections, Sendai virus, Ubiquitin-Protein Ligases
Adaptor Proteins, Signal Transducing, Animals, Cyclic AMP-Dependent Protein Kinase Catalytic Subunits, HEK293 Cells, Humans, Immunity, Innate, Immunoblotting, Immunoprecipitation, Membrane Proteins, Mice, Phosphorylation, Respirovirus Infections, Sendai virus, Ubiquitin-Protein Ligases
PLoS Pathog.
Date: Sep. 01, 2017
PubMed ID: 28934360
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