Hepatitis C virus NS5A protein is phosphorylated by casein kinase II

被引:65
作者
Kim, J [1 ]
Lee, D [1 ]
Choe, J [1 ]
机构
[1] Korea Adv Inst Sci & Technol, Dept Biol Sci, Taejon 305701, South Korea
关键词
D O I
10.1006/bbrc.1999.0460
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hepatitis C virus (HCV) has a positive-strand RNA genome that encodes a polyprotein, which is posttranslationally processed by cellular and viral proteinases into three structural and six non-structural (NS) proteins. The NS5A protein, expressed in mammalian cells, exists as two phosphorylated forms of 56 kDa and 58 kDa. In this study, we provide evidence for a stable association between NS5A and a protein kinase from rat-1 cells by affinity to immobilized glutathione-S-transferase (GST)-NS5A fusion protein. This protein kinase was associated through the N-terminus of NS5A and was not regulated by cell cycle. The GST-NS5A was also phosphorylated in vitro by the purified casein kinase II (CKII), a member of the CMCG kinase family. Since CKII and the NS5A-associated protein kinase have the same molecular size and property by In-gel kinase assay and an inhibitor treatment test, we conclude that HCV NS5A protein is phosphorylated by CKII. (C) 1999 Academic Press.
引用
收藏
页码:777 / 781
页数:5
相关论文
共 21 条
[1]   The N-terminal region of hepatitis C virus-encoded NS5A is important for NS4A-dependent phosphorylation [J].
Asabe, SI ;
Tanji, Y ;
Satoh, S ;
Kaneko, T ;
Kimura, K ;
Shimotohno, K .
JOURNAL OF VIROLOGY, 1997, 71 (01) :790-796
[2]   CHARACTERIZATION OF ROUS-SARCOMA VIRUS SRC GENE PRODUCTS SYNTHESIZED INVITRO [J].
BEEMON, K ;
HUNTER, T .
JOURNAL OF VIROLOGY, 1978, 28 (02) :551-566
[3]   Activation of nuclear transcription factor NF-κB by interleukin-1 is accompanied by casein kinase II-mediated phosphorylation of the p65 subunit [J].
Bird, TA ;
Schooley, K ;
Dower, SK ;
Hagen, H ;
Virca, GD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (51) :32606-32612
[4]   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
[5]   GENETIC ORGANIZATION AND DIVERSITY OF THE HEPATITIS-C VIRUS [J].
CHOO, QL ;
RICHMAN, KH ;
HAN, JH ;
BERGER, K ;
LEE, C ;
DONG, C ;
GALLEGOS, C ;
COIT, D ;
MEDINASELBY, A ;
BARR, PJ ;
WEINER, AJ ;
BRADLEY, DW ;
KUO, G ;
HOUGHTON, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (06) :2451-2455
[6]   CHARACTERIZATION OF THE HEPATITIS-C VIRUS-ENCODED SERINE PROTEINASE - DETERMINATION OF PROTEINASE-DEPENDENT POLYPROTEIN CLEAVAGE SITES [J].
GRAKOUI, A ;
MCCOURT, DW ;
WYCHOWSKI, C ;
FEINSTONE, SM ;
RICE, CM .
JOURNAL OF VIROLOGY, 1993, 67 (05) :2832-2843
[7]  
HATHAWAY GM, 1980, J BIOL CHEM, V255, P8038
[8]  
HATHAWAY GM, 1982, CURR TOP CELL REGUL, V21, P101
[9]   GENE-MAPPING OF THE PUTATIVE STRUCTURAL REGION OF THE HEPATITIS-C VIRUS GENOME BY INVITRO PROCESSING ANALYSIS [J].
HIJIKATA, M ;
KATO, N ;
OOTSUYAMA, Y ;
NAKAGAWA, M ;
SHIMOTOHNO, K .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (13) :5547-5551
[10]   Characterization of the nuclear localization signal and subcellular distribution of hepatitis C virus nonstructural protein NS5A [J].
Ide, Y ;
Zhang, LW ;
Chen, M ;
Inchauspe, G ;
Bahl, C ;
Sasaguri, Y ;
Padmanabhan, R .
GENE, 1996, 182 (1-2) :203-211