SENP2 negatively regulates cellular antiviral response by deSUMOylating IRF3 and conditioning it for ubiquitination and degradation
doi: 10.1093/jmcb/mjr020
pmid: 22028379
SENP2 negatively regulates cellular antiviral response by deSUMOylating IRF3 and conditioning it for ubiquitination and degradation
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.
- Shanghai Jiao Tong University China (People's Republic of)
- Wuhan University China (People's Republic of)
Mice, Knockout, Ubiquitination, Sumoylation, Interferon-beta, Virus Replication, Sendai virus, Immunity, Innate, Cysteine Endopeptidases, Mice, HEK293 Cells, Multienzyme Complexes, Endopeptidases, Small Ubiquitin-Related Modifier Proteins, Animals, Humans, Interferon Regulatory Factor-3, RNA Interference, Signal Transduction
Mice, Knockout, Ubiquitination, Sumoylation, Interferon-beta, Virus Replication, Sendai virus, Immunity, Innate, Cysteine Endopeptidases, Mice, HEK293 Cells, Multienzyme Complexes, Endopeptidases, Small Ubiquitin-Related Modifier Proteins, Animals, Humans, Interferon Regulatory Factor-3, RNA Interference, Signal Transduction
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