Key result
Respirovirus C protein binds to IFNAR2 and inhibits IFN-α-stimulated tyrosine phosphorylation of receptor-associated kinases JAK1 and TYK2, thereby blocking JAK-STAT signaling.
Why the study?
Respirovirus C protein inhibits IFN-stimulated STAT tyrosine phosphorylation, but the underlying mechanism was poorly understood.
Respirovirus C protein blocks JAK-STAT signaling by binding to IFNAR2 and inhibiting activation of JAK1 and TYK2.
Suggests target for blocking viral IFN suppression; leaves open whether this applies to human respirovirus disease.
Respirovirus C protein blocks the type I interferon (IFN)-stimulated activation of the JAK-STAT pathway. It has been reported that C protein inhibits IFN-α-stimulated tyrosine phosphorylation of STATs, but the underlying mechanism is poorly understood. Here, we show that the C protein of Sendai virus (SeV), a member of the Respirovirus genus, binds to the IFN receptor subunit IFN-α/β receptor subunit (IFNAR)2 and inhibits IFN-α-stimulated tyrosine phosphorylation of the upstream receptor-associated kinases, JAK1 and TYK2. Analysis of various SeV C mutant (Cm) proteins demonstrates the importance of the inhibitory effect on receptor-associated kinase phosphorylation for blockade of JAK-STAT signaling. Furthermore, this inhibitory effect and the IFNAR2 binding capacity are observed for all the respirovirus C proteins examined. Our results suggest that respirovirus C protein inhibits activation of the receptor-associated kinases JAK1 and TYK2 possibly through interaction with IFNAR2.
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Kitagawa et al. (2019) studied this question. Respirovirus C protein was evaluated on Inhibition of IFN-α-stimulated tyrosine phosphorylation of JAK1 and TYK2. Respirovirus C protein binds to IFNAR2 and inhibits IFN-α-stimulated tyrosine phosphorylation of receptor-associated kinases JAK1 and TYK2, thereby blocking JAK-STAT signaling.
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