| Literature DB >> 26363073 |
Li Huang1, Qinfang Liu1, Lijie Zhang1, Quan Zhang2, Liang Hu1, Changyao Li1, Shengnan Wang1, Jiangnan Li1, Yuanfeng Zhang1, Huibin Yu1, Yan Wang3, Zhaohua Zhong4, Tao Xiong5, Xueshan Xia6, Xiaojun Wang1, Li Yu1, Guohua Deng1, Xuehui Cai1, Shangjin Cui7, Changjiang Weng8.
Abstract
TRAF family member-associated NF-κB activator (TANK) is a negative regulator of canonical NF-κB signaling in the Toll-like receptor- and B-cell receptor-mediated signaling pathways. However, functions of TANK in viral infection-mediated NF-κB activation remain unclear. Here, we reported that TANK was cleaved by encephalomyocarditis virus 3C at the 197 and 291 glutamine residues, which depends on its cysteine protease activity. In addition, encephalomyocarditis virus 3C impaired the ability of TANK to inhibit TRAF6-mediated NF-κB signaling. Interestingly, we found that several viral proteases encoded by the foot and mouth disease virus, porcine reproductive and respiratory syndrome virus, and equine arteritis virus also cleaved TANK. Our results suggest that TANK is a novel target of some viral proteases, indicating that some positive RNA viruses have evolved to utilize their major proteases to regulate NF-κB activation.Entities:
Keywords: NF-kappa B (NF-KB); cell signaling; immunology; viral protease; virus
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Year: 2015 PMID: 26363073 PMCID: PMC4646013 DOI: 10.1074/jbc.M115.660761
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157