A comprehensive analysis of recruitment and transactivation potential of K-Rta and K-bZIP during reactivation of Kaposi's sarcoma-associated herpesvirus

被引:52
作者
Ellison, Thomas J. [1 ]
Izumiya, Yoshihiro [1 ,2 ]
Izumiya, Chie [1 ]
Luciw, Paul A. [3 ,4 ]
Kung, Hsing-Jien [1 ]
机构
[1] Univ Calif Davis, Sch Med, UC Davis Canc Ctr, Dept Biol Chem, Sacramento, CA 95817 USA
[2] Univ Calif Davis, Sch Med, UC Davis Canc Ctr, Dept Dermatol, Sacramento, CA 95817 USA
[3] Univ Calif Davis, Ctr Comparat Med, Davis, CA 95616 USA
[4] Univ Calif Davis, Dept Pathol, Davis, CA 95616 USA
基金
美国国家卫生研究院;
关键词
Kaposi's sarcoma; KSHV; HHV-8; Transcription; Chromatin immunoprecipitation; Gene expression; K-Rta/ORF50; K-bZIP/K8; Microarray; Chromatin; EPSTEIN-BARR-VIRUS; LYTIC SWITCH PROTEIN; DEPENDENT DNA-REPLICATION; GENE-EXPRESSION; TRANSCRIPTIONAL REPRESSION; CELLULAR-PROTEIN; PROMOTER; ACTIVATION; BINDING; LATENCY;
D O I
10.1016/j.virol.2009.02.016
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 the etiologic agent of Kaposi's sarcoma. K-Rta and K-bZIP are two major vital transcription factors that control reactivation of this virus. Here we report a genome-wide analysis of transcriptional capacity by evaluation of a comprehensive library of 83 putative KSHV promoters. In reporter assays, 34 viral promoters were activated by K-Rta, whereas K-bZIP activated 21 promoters. When K-Rta and K-bZIP were combined, 3 K-Rta responsive promoters were repressed by K-bZIP. The occupancy of K-Rta and K-bZIP across KSHV promoters was analyzed by chromatin immunoprecipitation with a viral promoter-chip in BCBL-1 cells. In addition, acetylation of local histories was examined to determine accessibility of promoters during latency and reactivation. Finally, 10 promoters were selected to study the dynamics of transcription factor recruitment. This study provides a comprehensive overview of the responsiveness of KSHV promoters to K-Rta and K-bZIP, and describes key chromatin changes during viral reactivation. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:76 / 88
页数:13
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