| Literature DB >> 27033607 |
Yangchao Dong1, Wei Ye1, Jing Yang1, Peijun Han1, Yuan Wang1, Chuantao Ye1, Daihui Weng1, Fanglin Zhang1, Zhikai Xu2, Yingfeng Lei3.
Abstract
Successful DENV infection relies on its ability to evade the host innate immune system. By using iTRAQ labeling followed by LC-MS/MS analysis, DDX21 was identified as a new host RNA helicase involved in the DENV life cycle. In DENV infected cells, DDX21 translocates from nucleus to cytoplasm to active the innate immune response and thus inhibits DENV replication in the early stages of infection. DDX21 is then degraded by the viral NS2B-NS3 protease complex and the innate immunity is thus subverted to facilitate DENV replication. The results reveal a new mechanism in which DENV subverts the host innate immune system to facilitate its replication in host cells.Entities:
Keywords: DDX21; DENV; Innate immune response; NS2B/3 protease; iTRAQ
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Year: 2016 PMID: 27033607 DOI: 10.1016/j.bbrc.2016.03.120
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575