Wu Ting-Ting, Park Tina, Kim Hana, Tran Thuy, Tong Leming, Martinez-Guzman DeeAnn, Reyes Nichole, Deng Hongyu, Sun Ren
Department of Molecular and Medical Pharmacology, University of California at Los Angeles, Los Angeles, California 90095, USA.
J Virol. 2009 Mar;83(5):2265-73. doi: 10.1128/JVI.01785-08. Epub 2008 Dec 17.
A hallmark of productive infection by DNA viruses is the coupling of viral late gene expression to genome replication. Here we report the identification of open reading frame 30 (ORF30) and ORF34 as viral trans factors crucial for activating late gene transcription following viral DNA replication during lytic infection of murine gammaherpesvirus 68 (MHV-68). The mutant virus lacking either ORF30 or ORF34 underwent normal DNA replication but failed to express viral late gene transcripts, leading to nonproductive infection. In a reporter assay system, ORF30 and ORF34 were required for MHV-68 to activate the viral late gene promoters. Furthermore, studies using chromatin immunoprecipitation assays showed that the recruitment of RNA polymerase II to the viral late promoters during lytic infection was significantly reduced in the absence of ORF30 or ORF34. Together, the results suggest that ORF30 and ORF34 may play an important role in the assembly of the transcription initiation complex at the late gene promoters. Our discovery of the viral mutants that uncouple late gene transcription from DNA replication lays an important foundation to dissect the mechanism of this critical step of gene expression regulation.
DNA病毒有效感染的一个标志是病毒晚期基因表达与基因组复制的偶联。在此,我们报告了开放阅读框30(ORF30)和开放阅读框34被鉴定为病毒反式作用因子,它们对于小鼠γ疱疹病毒68(MHV - 68)裂解感染期间病毒DNA复制后激活晚期基因转录至关重要。缺失ORF30或ORF34的突变病毒进行了正常的DNA复制,但未能表达病毒晚期基因转录本,导致感染无 productive。在报告基因检测系统中,MHV - 68激活病毒晚期基因启动子需要ORF30和ORF34。此外,使用染色质免疫沉淀分析的研究表明,在裂解感染期间,在没有ORF30或ORF34的情况下,RNA聚合酶II募集到病毒晚期启动子的情况显著减少。总之,结果表明ORF30和ORF34可能在晚期基因启动子处转录起始复合物的组装中起重要作用。我们发现了使晚期基因转录与DNA复制解偶联的病毒突变体,为剖析这一基因表达调控关键步骤的机制奠定了重要基础。