Kaposi's sarcoma-associated herpesvirus K-bZIP is a coregulator of K-Rta: Physical association and promoter-dependent transcriptional repression

被引:95
作者
Izumiya, Y
Lin, SF
Ellison, T
Chen, LY
Izumiya, C
Luciw, P
Kung, HJ
机构
[1] Univ Calif Davis, Ctr Canc, Sch Med, Dept Biol Chem, Sacramento, CA 95817 USA
[2] Univ Calif Davis, Ctr Comparat Med, Davis, CA 95616 USA
关键词
D O I
10.1128/JVI.77.2.1441-1451.2003
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Kaposi's sarcoma-associated herpesvirus (KSHV) is a human gammaherpesvirus that has been implicated in the pathogenesis of Kaposi's sarcoma and B-cell neoplasms. The genomic organization of KSHV is similar to that of Epstein-Barr virus (EBV). EBV encodes two transcriptional factors, Rta and Zta, which functionally interact to transactivate EBV genes during replication and reactivation from latency. KSHV encodes a basic leucine zipper protein (K-bZIP), a homologue of EBV Zta, and K-Rta, the homologue of EBV Rta. EBV Rta and Zta are strong transcriptional transactivators. Although there is ample evidence that K-Rta is a potent transactivator, the role of K-bZIP as a transcriptional factor is much less clear. In this study, we report that K-bZIP modulates K-Rta function. We show that K-bZIP directly interacts with K-Rta in vivo and in vitro. This association is specific, requiring the basic domain (amino acids 122 to 189) of K-bZIP and a specific region (amino acids 499 to 550) of K-Rta, and can be detected with K-bZIP and K-Rta endogenously expressed in BCBL-1 cells treated with tetradecanoyl phorbol acetate. The functional relevance of this association was revealed by the observation that K-bZIP represses the transactivation of the ORF57 promoter by K-Rta in a dose-dependent manner. K-bZIP lacking the interaction domain fails to repress K-Rta-mediated transactivation; this finding attests to the specificity of the repression. Interestingly, this repression is not observed for the promoter of polyadenylated nuclear (PAN) RNA, another target of K-Rta; thus, repression is promoter dependent. Finally, we provide evidence that the modulation of K-Rta by K-bZIP also occurs in vivo during reactivation of the viral genome in BCBL-1 cells. When K-bZIP is overexpressed in BCBL-1 cells, the level of expression of ORF57 but not PAN RNA is repressed. These data support the model that one function of K-bZIP is to modulate the activity of the transcriptional transactivator K-Rta.
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页码:1441 / 1451
页数:11
相关论文
共 41 条
[1]   Human herpesvirus-8/Kaposi's sarcoma-associated herpesvirus in organ transplant patients with immunosupression [J].
Alkan, S ;
Karcher, DS ;
Ortiz, A ;
Khalil, S ;
Akhtar, M ;
Ali, MA .
BRITISH JOURNAL OF HAEMATOLOGY, 1997, 96 (02) :412-414
[2]   KAPOSIS SARCOMA-ASSOCIATED HERPESVIRUS INFECTS ENDOTHELIAL AND SPINDLE CELLS [J].
BOSHOFF, C ;
SCHULZ, TF ;
KENNEDY, MM ;
GRAHAM, AK ;
FISHER, C ;
THOMAS, A ;
MCGEE, JO ;
WEISS, RA ;
OLEARY, JJ .
NATURE MEDICINE, 1995, 1 (12) :1274-1278
[3]   KAPOSIS SARCOMA-ASSOCIATED HERPESVIRUS-LIKE DNA-SEQUENCES IN AIDS-RELATED BODY-CAVITY-BASED LYMPHOMAS [J].
CESARMAN, E ;
CHANG, Y ;
MOORE, PS ;
SAID, JW ;
KNOWLES, DM .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 332 (18) :1186-1191
[4]   Synergistic interactions between over-lapping binding sites for the serum response factor and ELK-1 proteins mediate both basal enhancement and phorbol ester responsiveness of primate cytomegalovirus major immediate-early promoters in monocyte and T-lymphocyte cell types [J].
Chan, YJ ;
Chiou, CJ ;
Huang, Q ;
Hayward, GS .
JOURNAL OF VIROLOGY, 1996, 70 (12) :8590-8605
[5]   Open reading frame 50 protein of Kaposi's sarcoma-associated herpesvirus directly activates the viral PAN and K12 genes by binding to related response elements [J].
Chang, PJ ;
Shedd, D ;
Gradoville, L ;
Cho, MS ;
Chen, LW ;
Chang, J ;
Miller, G .
JOURNAL OF VIROLOGY, 2002, 76 (07) :3168-3178
[6]   IDENTIFICATION OF HERPESVIRUS-LIKE DNA-SEQUENCES IN AIDS-ASSOCIATED KAPOSIS-SARCOMA [J].
CHANG, Y ;
CESARMAN, E ;
PESSIN, MS ;
LEE, F ;
CULPEPPER, J ;
KNOWLES, DM ;
MOORE, PS .
SCIENCE, 1994, 266 (5192) :1865-1869
[7]   Transcriptional regulation of the Kaposi's sarcoma-associated herpesvirus viral interferon regulatory factor gene [J].
Chen, JG ;
Ueda, K ;
Sakakibara, S ;
Okuno, T ;
Yamanishi, K .
JOURNAL OF VIROLOGY, 2000, 74 (18) :8623-8634
[8]   BOTH EPSTEIN-BARR-VIRUS (EBV)-ENCODED TRANS-ACTING FACTORS, EB1 AND EB2, ARE REQUIRED TO ACTIVATE TRANSCRIPTION FROM AN EBV EARLY PROMOTER [J].
CHEVALLIERGRECO, A ;
MANET, E ;
CHAVRIER, P ;
MOSNIER, C ;
DAILLIE, J ;
SERGEANT, A .
EMBO JOURNAL, 1986, 5 (12) :3243-3249
[9]   ACTIVATION OF EXPRESSION OF LATENT EPSTEIN-BARR HERPESVIRUS AFTER GENE-TRANSFER WITH A SMALL CLONED SUBFRAGMENT OF HETEROGENEOUS VIRAL-DNA [J].
COUNTRYMAN, J ;
MILLER, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (12) :4085-4089
[10]   AN ENHANCER WITHIN THE DIVERGENT PROMOTER OF EPSTEIN-BARR VIRUS RESPONDS SYNERGISTICALLY TO THE R-TRANSACTIVATORS AND Z-TRANSACTIVATORS [J].
COX, MA ;
LEAHY, J ;
HARDWICK, JM .
JOURNAL OF VIROLOGY, 1990, 64 (01) :313-321