期刊
JOURNAL OF BIOLOGICAL CHEMISTRY
卷 288, 期 18, 页码 12596-12604出版社
AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.M112.444794
关键词
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资金
- Chinese Ministry of Science and Technology [2012CB910201, 2010DFA31100]
- National Science Foundation of China [91029302, 31130020, 31221061]
- Chinese 111 project [B06018]
- Ministry of Education of China
Viral infection causes activation of the transcription factor IRF3, which is critical for production of type I interferons (IFNs) and innate antiviral immune response. How virus-induced type I IFN signaling is controlled is not fully understood. Here we identified the transcription factor FoxO1 as a negative regulator for virus-triggered IFN-beta induction. Overexpression of FoxO1 inhibited virus-triggered ISRE activation, IFN-beta induction as well as cellular antiviral response, whereas knockdown of FoxO1 had opposite effects. FoxO1 interacted with IRF3 in a viral infection-dependent manner and promoted K48-linked polyubiquitination and degradation of IRF3 in the cytosol. Furthermore, FoxO1-mediated degradation of IRF3 was independent of the known E3 ubiquitin ligases for IRF3, including RBCK1 and RAUL. Our findings thus suggest that FoxO1 negatively regulates cellular antiviral response by promoting IRF3 ubiquitination and degradation, providing a previously unknown mechanism for control of type I IFN induction and cellular antiviral response.
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