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SENP2 negatively regulates cellular antiviral response by deSUMOylating IRF3 and conditioning it for ubiquitination and degradation Free
Yong Ran1, Tian-Tian Liu1, Qian Zhou1, Shu Li1, Ai-Ping Mao1, Ying Li1, Li-Juan Liu1, Jin-Ke Cheng2, and Hong-Bing Shu1,*
1College of Life Sciences, Wuhan University, Wuhan 430072, China
2Department of Biochemistry and Molecular Cell Biology, School of Medicine, Shanghai Jiao Tong University, Shanghai 200025, China *Correspondence to:Hong-Bing Shu, E-mail: shuh@whu.edu.cn
J Mol Cell Biol, Volume 3, Issue 5, October 2011, 283-292,  https://doi.org/10.1093/jmcb/mjr020
Keyword: SENP2, IRF3, deSUMOylation, ubiquitination, innate immunity
Transcription factor IRF3-mediated type I interferon induction is essential for antiviral innate immunity. We identified the deSUMOylating enzyme Sentrin/SUMO-specific protease (SENP) 2 as a negative regulator of virus-triggered IFN-β induction. Overexpression of SENP2 caused IRF3 deSUMOylation, K48-linked ubiquitination, and degradation, whereas depletion of SENP2 had opposite effects. Both the SUMOylation and K48-linked ubiquitination of IRF3 occurred at lysines 70 and 87, and these processes are competitive. The level of virus-triggered IFN-β was markedly up-regulated and viral replication was reduced in SENP2-deficient cells comparing with wild-type controls. Our findings suggest that SENP2 regulates antiviral innate immunity by deSUMOylating IRF3 and conditioning it for ubiquitination and degradation, and provide an example of cross-talk between the ubiquitin and SUMO pathways in innate immunity.