Hepatitis C virus core protein interacts with 14-3-3 protein and activates the kinase Raf-1

被引:129
作者
Aoki, H
Hayashi, J
Moriyama, M
Arakawa, Y
Hino, O
机构
[1] Japanese Fdn Canc Res, Inst Canc, Dept Expt Pathol, Toshima Ku, Tokyo 1708455, Japan
[2] Nihon Univ, Sch Med, Dept Internal Med 3, Itabashi Ku, Tokyo 1738610, Japan
关键词
D O I
10.1128/JVI.74.4.1736-1741.2000
中图分类号
Q93 [微生物学];
学科分类号
071005 [微生物学]; 100705 [微生物与生化药学];
摘要
Persistent hepatitis C virus (HCV) infection is a major cause of chronic liver dysfunction in humans and is epidemiologically protein has been reported to be implicated in cell growth regulation both in vitro and in vivo, although mechanisms explaining those effects are still unclear. In the present study, we identified that members of the 14-3-3 protein family associate with HCV core protein. 14-3-3 protein bound to HCV core protein in a phosphoserine-dependent manner, Introduction of HCV core protein caused a substantial increase in Raf-1 kinase activity in HepG2 cells and in a yeast genetic assay. Furthermore, the HCV core-14-3-3 interaction was essential for Raf-1 kinase activation by HCV core protein. These results suggest that HCV core protein may represent a novel type of Raf-1 kinase-activating protein through its interaction with 14-3-3 protein and may contribute to hepatocyte growth regulation.
引用
收藏
页码:1736 / 1741
页数:6
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