Herpes virus proteins BICP0 and BICP0 can activate NF-κB by catalyzing IκBα ubiquitination

被引:61
作者
Diao, LR
Zhang, BH
Fan, JK
Gao, X
Sun, SG
Yang, K
Dan, X
Jin, NH
Geng, YQ
Wang, C
机构
[1] Chinese Acad Sci, Shanghai Inst Biol Sci, Inst Biochem & Cell Biol, Mol & Cellular Biol Lab, Shanghai 200031, Peoples R China
[2] Nankai Univ, Coll Life Sci, Tianjin 300071, Peoples R China
基金
中国国家自然科学基金;
关键词
herpes virus; ICP0; BICP0; ubiquitin; I kappa B alpha;
D O I
10.1016/j.cellsig.2004.07.003
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The immediate early proteins ICPO and BICPO from Herpes virus are promiscuous activators of both viral and cellular genes and play a critical role in virus life cycle. Here we report that ICPO and BICPO could induce NF-kappaB translocation from cytoplasm into nucleus and strongly activate NF-kappaB responsive genes specifically. This process was dependent on the RING domain of both proteins. In addition, ICPO interacted specifically with IkappaBalpha and its activating effect was attenuated by Ubch5A(C85A) and MG132, but not by IkappaBalpha(S32A/S36A). Remarkably, IkappaBalpha was poly-ubiquitinated by both ICPO and BICPO, in vitro and in vivo. These data indicate that ICPO and BICPO, functioning as ubiquitin ligases, are bona fide activators of NF-kappaB signaling pathway. Our study identifies a new way ICPO and BICPO explore to regulate gene expression. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:217 / 229
页数:13
相关论文
共 42 条
[1]  
Bate MW, 2000, METH MOL B, V99, P277
[2]   The herpes simplex virus type 1 (HSV-1) regulatory protein ICP0 interacts with and ubiquitinates p53 [J].
Boutell, C ;
Everett, RD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (38) :36596-36602
[3]   Herpes simplex virus type 1 immediate-early protein ICP0 and its isolated RING finger domain act as ubiquitin E3 ligases in vitro [J].
Boutell, C ;
Sadis, S ;
Everett, RD .
JOURNAL OF VIROLOGY, 2002, 76 (02) :841-850
[4]   Herpes virus induced proteasome-dependent degradation of the nuclear bodies-associated PML and Sp100 proteins [J].
Chelbi-Alix, MK ;
de Thé, H .
ONCOGENE, 1999, 18 (04) :935-941
[5]   NF-κB signaling:: Many roads lead to Madrid [J].
Dixit, V ;
Mak, TW .
CELL, 2002, 111 (05) :615-619
[6]   HSV-1 IE PROTEIN VMW110 CAUSES REDISTRIBUTION OF PML [J].
EVERETT, RD ;
MAUL, GG .
EMBO JOURNAL, 1994, 13 (21) :5062-5069
[7]   The disruption of ND10 during herpes simplex virus infection correlates with the Vmw11O- and proteasome-dependent loss of several PML isoforms [J].
Everett, RD ;
Freemont, P ;
Saitoh, H ;
Dasso, M ;
Orr, A ;
Kathoria, M ;
Parkinson, J .
JOURNAL OF VIROLOGY, 1998, 72 (08) :6581-6591
[8]  
Everett RD, 2000, BIOESSAYS, V22, P761, DOI 10.1002/1521-1878(200008)22:8<761::AID-BIES10>3.0.CO
[9]  
2-A
[10]   A novel ubiquitin-specific protease is dynamically associated with the PML nuclear domain and binds to a herpesvirus regulatory protein [J].
Everett, RD ;
Meredith, M ;
Orr, A ;
Cross, A ;
Kathoria, M ;
Parkinson, J .
EMBO JOURNAL, 1997, 16 (07) :1519-1530