4.8 Article

ISG56 is a negative-feedback regulator of virus-triggered signaling and cellular antiviral response

出版社

NATL ACAD SCIENCES
DOI: 10.1073/pnas.0900818106

关键词

interferon; MITA; negative-feedback regulation; IRF3; NF-kappa B

资金

  1. Chinese 973 Program [2006CB504301]
  2. National Natural Science Foundation of China [30630019, 30700431]
  3. Chinese 863 Program [2006AA02A306]
  4. Chinese Science and Technology Key Project [2008ZX10002-014]

向作者/读者索取更多资源

IFN-stimulated gene 56 (ISG56) is one of the first identified proteins induced by viruses and type I IFNs. In this study, we identified ISG56 as a virus-induced protein associated with MITA, an adapter protein involved in virus-triggered induction of type I IFNs. Overexpression of ISG56 inhibited Sendai virus-triggered activation of IRF3, NF-kappa B, and the IFN-beta promoter, whereas knockdown of ISG56 had opposite effects. Consistently, overexpression of ISG56 reversed cytoplasmic poly(I:C)-induced inhibition of vesicular stomatitis virus (VSV) replication, whereas knockdown of ISG56 inhibited VSV replication. Competitive coimmunoprecipitation experiments indicated that ISG56 disrupted the interactions between MITA and VISA or TBK1, two components in the virus-triggered IFN signaling pathways. These results suggest that ISG56 is a mediator of negative-feedback regulation of virus-triggered induction of type I IFNs and cellular antiviral responses.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据