溶解循环
BZLF1型
生物
爱泼斯坦-巴尔病毒
交易激励
基因敲除
病毒潜伏期
病毒学
分子生物学
转录因子
抄写(语言学)
组蛋白
病毒
细胞培养
DNA
疱疹病毒科
遗传学
病毒复制
基因
病毒性疾病
语言学
哲学
作者
Huey‐Huey Chua,Hsin‐Yi Chiu,Sue‐Jane Lin,Pei‐Lun Weng,Jiun‐Han Lin,Shao‐Wen Wu,Shu‐Chun Tsai,Ching‐Hwa Tsai
摘要
Abstract Epstein–Barr virus (EBV) belongs to the gammaherpesvirus family. To produce infectious progeny, EBV reactivates from latency into the lytic cycle by expressing the determinative lytic transactivator, Zta. In the presence of histone deacetylase inhibitor (HDACi), p53 is a prerequisite for the initiation of the EBV lytic cycle by facilitating the expression of Zta. In this study, a serial mutational analysis of Zta promoter (Zp) indicated an important role for the ZID element in responding to HDACi induction and p53 binds to this ZID element together with Sp1, a universal transcription factor. Abolition of the DNA‐binding ability of Sp1 reduces the inducibility of ZID by HDACi and also reduces the amount of p53 binding to ZID. Finally, it was shown that EBV in p53‐positive‐lymphoblastoid cell lines (LCLs) can enter into the lytic cycle spontaneously; however, knockdown of p53 in LCLs leads to retardation of EBV reactivation. J. Med. Virol. 84: 1279–1288, 2012. © 2012 Wiley Periodicals, Inc.
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