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Negative Regulation of Nmi on Virus-Triggered Type I IFN Production by Targeting IRF7
Author(s) -
Jie Wang,
Bo Yang,
Yu Hu,
Yuhan Zheng,
Haiyan Zhou,
Yanming Wang,
Yonglei Ma,
Kairui Mao,
Leilei Yang,
Guomei Lin,
Yongyong Ji,
Xiaodong Wu,
Bing Sun
Publication year - 2013
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.1300740
Subject(s) - irf7 , sendai virus , vesicular stomatitis virus , biology , regulator , gene knockdown , virology , virus , microbiology and biotechnology , immune system , innate immune system , cell culture , immunology , gene , biochemistry , genetics
Viral infection causes host cells to produce type I IFNs, which play a critical role in viral clearance. IFN regulatory factor (IRF) 7 is the master regulator of type I IFN-dependent immune responses. In this article, we report that N-Myc and STATs interactor (Nmi), a Sendai virus-inducible protein, interacted with IRF7 and inhibited virus-triggered type I IFN production. The overexpression of Nmi inhibited the Sendai virus-triggered induction of type I IFNs, whereas the knockdown of Nmi promoted IFN production. Furthermore, the enhanced production of IFNs resulting from Nmi knockdown was sufficient to protect cells from infection by vesicular stomatitis virus. In addition, Nmi was found to promote the K48-linked ubiquitination of IRF7 and the proteasome-dependent degradation of this protein. Finally, an impairment of antiviral responses is also detectable in Nmi-transgenic mice. These findings suggest that Nmi is a negative regulator of the virus-triggered induction of type I IFNs that targets IRF7.

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