Chang Shih-Shin, Lo You-Chang, Chua Huey-Huey, Chiu Hsin-Yi, Tsai Shu-Chun, Chen Jen-Yang, Lo Kwok-Wai, Tsai Ching-Hwa
Graduate Institute of Microbiology, College of Medicine, National Taiwan University, No. 1, Sec. 1, Ren-Ai Rd., Taipei 10051, Taiwan.
J Virol. 2008 Aug;82(15):7745-51. doi: 10.1128/JVI.02717-07. Epub 2008 May 21.
The tumor suppressor gene p53 plays a central role in the maintenance of normal cell growth and genetic integrity, while its impact on the Epstein-Barr virus (EBV) life cycle remains elusive. We found that p53 is important for histone deacetylase inhibitor-induced EBV lytic gene expression in nasopharyngeal carcinoma cells. Restoration of p53 in p53-null, EBV-infected H1299 cells augments the potential for viral lytic cycle initiation. Evidence from reporter assays demonstrated that p53 contributes to the expression of the immediate-early viral Zta gene. Further analysis indicated that the DNA-binding ability of p53 and phosphorylation of Ser392 may be critical. This study provides the first evidence that p53 is involved in the regulation of EBV lytic cycle initiation.
肿瘤抑制基因p53在维持正常细胞生长和遗传完整性方面发挥着核心作用,但其对爱泼斯坦-巴尔病毒(EBV)生命周期的影响仍不清楚。我们发现p53对组蛋白去乙酰化酶抑制剂诱导的鼻咽癌细胞中EBV裂解基因表达很重要。在p53缺失、EBV感染的H1299细胞中恢复p53可增强病毒裂解周期启动的可能性。报告基因检测的证据表明p53有助于病毒早期即刻Zta基因的表达。进一步分析表明p53的DNA结合能力和Ser392的磷酸化可能至关重要。本研究首次提供了p53参与调控EBV裂解周期启动的证据。