Wiedmer Andreas, Wang Pu, Zhou Jing, Rennekamp Andrew J, Tiranti Valeria, Zeviani Massimo, Lieberman Paul M
The Wistar Institute, 3601 Spruce St., Philadelphia, PA 19104, USA.
J Virol. 2008 May;82(9):4647-55. doi: 10.1128/JVI.02198-07. Epub 2008 Feb 27.
Disruption of cellular metabolic processes and usurpation of host proteins are hallmarks of herpesvirus lytic infection. Epstein-Barr virus (EBV) lytic replication is initiated by the immediate-early protein Zta. Zta is a multifunctional DNA binding protein that stimulates viral gene transcription, nucleates a replication complex at the viral origin of lytic replication, and inhibits cell cycle proliferation. To better understand these functions and identify cellular collaborators of Zta, we purified an epitope-tagged version of Zta in cells capable of supporting lytic replication. FLAG-tagged Zta was purified from a nuclear fraction using FLAG antibody immunopurification and peptide elution. Zta-associated proteins were isolated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and identified by mass spectrometry. The Zta-associated proteins included members of the HSP70 family and various single-stranded DNA and RNA binding proteins. The nuclear replication protein A subunits (RPA70 and RPA32) and the human mitochondrial single-stranded DNA binding protein (mtSSB) were confirmed by Western blotting to be specifically enriched in the FLAG-Zta immunopurified complex. mtSSB coimmunoprecipitated with endogenous Zta during reactivation of EBV-positive Burkitt lymphoma and lymphoblastoid cell lines. Small interfering RNA depletion of mtSSB reduced Zta-induced lytic replication of EBV but had only a modest effect on transcription activation function. A point mutation in the Zta DNA binding domain (C189S), which is known to reduce lytic cycle replication, eliminated mtSSB association with Zta. The predominantly mitochondrial localization of mtSSB was shifted to partly nuclear localization in cells expressing Zta. Mitochondrial DNA synthesis and genome copy number were reduced by Zta-induced EBV lytic replication. We conclude that Zta interaction with mtSSB serves the dual function of facilitating viral and blocking mitochondrial DNA replication.
细胞代谢过程的破坏和宿主蛋白的篡夺是疱疹病毒裂解感染的标志。爱泼斯坦-巴尔病毒(EBV)的裂解复制由立即早期蛋白Zta启动。Zta是一种多功能DNA结合蛋白,可刺激病毒基因转录,在裂解复制的病毒起源处形成复制复合物,并抑制细胞周期增殖。为了更好地理解这些功能并鉴定Zta的细胞协同因子,我们在能够支持裂解复制的细胞中纯化了一个带有表位标签的Zta版本。使用FLAG抗体免疫纯化和肽洗脱从核部分纯化了FLAG标签的Zta。通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳分离Zta相关蛋白,并通过质谱鉴定。Zta相关蛋白包括HSP70家族成员以及各种单链DNA和RNA结合蛋白。通过蛋白质印迹法证实核复制蛋白A亚基(RPA70和RPA32)和人线粒体单链DNA结合蛋白(mtSSB)在FLAG-Zta免疫纯化复合物中特异性富集。在EBV阳性伯基特淋巴瘤和成淋巴细胞系的重新激活过程中,mtSSB与内源性Zta共免疫沉淀。mtSSB的小干扰RNA缺失减少了Zta诱导的EBV裂解复制,但对转录激活功能只有适度影响。已知可减少裂解周期复制的Zta DNA结合域中的点突变(C189S)消除了mtSSB与Zta的结合。在表达Zta的细胞中,mtSSB主要的线粒体定位转移到部分核定位。Zta诱导的EBV裂解复制减少了线粒体DNA合成和基因组拷贝数。我们得出结论,Zta与mtSSB的相互作用具有促进病毒和阻断线粒体DNA复制的双重功能。