Hepatitis C virus core protein binds to a C-terminal region of NS5B RNA polymerase

被引:14
作者
Uchida, M
Hino, N
Yamanaka, T
Fukushima, H
Imanishi, T
Uchiyama, Y
Kodama, T
Doi, T
机构
[1] Osaka Univ, Grad Sch Pharmaceut Sci, Suita, Osaka 5650871, Japan
[2] Univ Tokyo, Adv Sci & Technol Res Ctr, Meguro Ku, Tokyo 1538904, Japan
关键词
NS5B-core protein complex; immunofluorescence analysis; immunoprecipitation analysis;
D O I
10.1016/S1386-6346(02)00005-0
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Hepatitis C virus (HCV) NS5B has been shown to exhibit RNA-dependent RNA polymerase activity for its viral RNA replication. In this study, we demonstrated the formation of a complex between NS5B and the core protein (NS5B-core protein complex) in mammalian cells, as determined by indirect immunofluorescence and immunoprecipitation analyses. The localization of the core protein was observed to change to the same locus in ER as NS5B locates by its coexpression with NS5B, indicating that the localization of the core protein is determined by NS5B. The truncated NS5B molecule lacking the C-terminal region did not form a complex with the core protein, suggesting that the C-terminal region of NS5B is essential for its interaction with the core protein. Moreover, the change in NS5B localization because of C-terminal deletion indicates that this region includes a certain signal for NS5B retention in ER. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:297 / 306
页数:10
相关论文
共 32 条
[1]   Hepatitis C virus core protein interacts with 14-3-3 protein and activates the kinase Raf-1 [J].
Aoki, H ;
Hayashi, J ;
Moriyama, M ;
Arakawa, Y ;
Hino, O .
JOURNAL OF VIROLOGY, 2000, 74 (04) :1736-1741
[2]   Identification and properties of the RNA-dependent RNA polymerase of hepatitis C virus [J].
Behrens, SE ;
Tomei, L ;
DeFrancesco, R .
EMBO JOURNAL, 1996, 15 (01) :12-22
[3]   Crystal structure of the RNA-dependent RNA polymerase of hepatitis C virus [J].
Bressanelli, S ;
Tomei, L ;
Roussel, A ;
Incitti, I ;
Vitale, RL ;
Mathieu, M ;
De Francesco, R ;
Rey, FA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (23) :13034-13039
[4]   Direct interaction of hepatitis C virus core protein with the cellular lymphotoxin-beta receptor modulates the signal pathway of the lymphotoxin-beta receptor [J].
Chen, CM ;
You, LR ;
Hwang, LH ;
Lee, YHW .
JOURNAL OF VIROLOGY, 1997, 71 (12) :9417-9426
[5]   ISOLATION OF A CDNA CLONE DERIVED FROM A BLOOD-BORNE NON-A, NON-B VIRAL-HEPATITIS GENOME [J].
CHOO, QL ;
KUO, G ;
WEINER, AJ ;
OVERBY, LR ;
BRADLEY, DW ;
HOUGHTON, M .
SCIENCE, 1989, 244 (4902) :359-362
[6]   Heterogeneous nuclear ribonucleoprotein I (hnRNP-I/PTB) selectively binds the conserved 3′ terminus of hepatitis C viral RNA [J].
Chung, RT ;
Kaplan, LM .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 254 (02) :351-362
[7]   AN N-TERMINAL DOMAIN OF THE SENDAI PARAMYXOVIRUS P-PROTEIN ACTS AS A CHAPERONE FOR THE NP PROTEIN DURING THE NASCENT CHAIN ASSEMBLY STEP OF GENOME REPLICATION [J].
CURRAN, J ;
MARQ, JB ;
KOLAKOFSKY, D .
JOURNAL OF VIROLOGY, 1995, 69 (02) :849-855
[8]  
Fan ZY, 1999, J MED VIROL, V59, P131, DOI 10.1002/(SICI)1096-9071(199910)59:2<131::AID-JMV1>3.3.CO
[9]  
2-3
[10]   BOTH THE N-TERMINAL AND THE C-TERMINAL DOMAINS OF THE NOMINAL PHOSPHOPROTEIN OF RABIES VIRUS ARE INVOLVED IN BINDING TO THE NUCLEOPROTEIN [J].
FU, ZF ;
ZHENG, YM ;
WUNNER, WH ;
KOPROWSKI, H ;
DIETZSCHOLD, B .
VIROLOGY, 1994, 200 (02) :590-597