Ubiquitin-Conjugating Enzyme 2S Enhances Viral Replication by Inhibiting Type I IFN Production through Recruiting USP15 to Deubiquitinate TBK1

文献类型： 外文期刊

第一作者： Huang, Li

作者： Huang, Li;Liu, Hongyang;Zhang, Kunli;Meng, Qingwen;Hu, Liang;Zhang, Yuanfeng;Xiang, Zhida;Li, Jiangnan;Bu, Zhigao;Weng, Changjiang;Liu, Hongyang;Xiang, Zhida;Yang, Yuying;Weng, Changjiang;Chen, Yali;Cui, Shangjin;Tang, Hong;Pei, Huadong;Pei, Huadong

作者机构：

期刊名称：CELL REPORTS （ 影响因子：9.423； 五年影响因子：10.394 ）

ISSN： 2211-1247

年卷期： 2020 年 32 卷 7 期

页码：

收录情况： SCI

摘要： Type I interferon (IFN) plays an essential role in the host innate immune responses. Several ubiquitin-conjugating enzyme (E2) family members were reported to regulate type I IFN production and host antiviral immune responses. However, the molecular mechanisms are still not fully understood. Here, we report that UBE2S acts as a negative regulator in the type I IFN signaling pathway. Ectopic expression of UBE2S inhibits host antiviral immune responses and enhances viral replications, whereas deficiency of UBE2S enhances host antiviral immune responses and suppresses viral replications both in vitro and in vivo. Inhibition of type I IFN production by UBE2S is independent on its E2 and E3 enzymic activity. Mechanistically, UBE2S interacts with TBK1 and recruits ubiquitin-specific protease 15 (USP15) to remove Lys63 (K63)-linked polyubiquitin chains of TBK1 Our findings reveal a role of the UBE2S-USP15-TBK1 axis in the regulation of host antiviral innate immune responses.

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