- Zhang, Qian;
- Meng, Fansen;
- Chen, Shasha;
- Plouffe, Steven W;
- Wu, Shiying;
- Liu, Shengduo;
- Li, Xinran;
- Zhou, Ruyuan;
- Wang, Junxian;
- Zhao, Bin;
- Liu, Jianming;
- Qin, Jun;
- Zou, Jian;
- Feng, Xin-Hua;
- Guan, Kun-Liang;
- Xu, Pinglong
The Hippo pathway senses cellular conditions and regulates YAP/TAZ to control cellular and tissue homeostasis, while TBK1 is central for cytosolic nucleic acid sensing and antiviral defence. The correlation between cellular nutrient/physical status and host antiviral defence is interesting but not well understood. Here we find that YAP/TAZ act as natural inhibitors of TBK1 and are vital for antiviral physiology. Independent of transcriptional regulation and through the transactivation domain, YAP/TAZ associate directly with TBK1 and abolish virus-induced TBK1 activation, by preventing TBK1 Lys63-linked ubiquitylation and the binding of adaptors/substrates. Accordingly, YAP/TAZ deletion/depletion or cellular conditions inactivating YAP/TAZ through Lats1/2 kinases relieve TBK1 suppression and boost antiviral responses, whereas expression of the transcriptionally inactive YAP dampens cytosolic RNA/DNA sensing and weakens the antiviral defence in cells and zebrafish. Thus, we describe a function of YAP/TAZ and the Hippo pathway in innate immunity, by linking cellular nutrient/physical status to antiviral host defence.