INSERM U758, Unité de Virologie humaine, Lyon, France.
J Virol. 2012 Jun;86(11):6023-32. doi: 10.1128/JVI.00159-12. Epub 2012 Mar 28.
That the expression of late genes is coupled to viral genome replication is well established for all herpesviruses, but the exact mechanisms of their regulation, especially by viral proteins, are poorly understood. Here, we report the identification of the Epstein-Barr virus (EBV) early protein BcRF1 as a viral factor crucial for the activation of late gene transcription following viral DNA replication during the productive cycle. In order to study the function of the BcRF1 protein, we constructed a recombinant EBV lacking this gene. In HEK293 cells, this recombinant virus underwent normal DNA replication during the productive cycle but failed to express high levels of late gene transcripts or proteins, resulting in a nonproductive infection. Interestingly, a TATT motif is present in the promoter of most EBV late genes, at the position of the TATA box. We show here that BcRF1 forms a complex with the TATT motif and that this interaction is required for activation of late viral gene expression. Moreover, our results suggest that BcRF1 acts via interaction with other viral proteins.
所有疱疹病毒的基因表达都与病毒基因组复制偶联,这一点已得到充分证实,但它们的调控机制,特别是病毒蛋白的调控机制,还知之甚少。在这里,我们报告了 Epstein-Barr 病毒(EBV)早期蛋白 BcRF1 的鉴定,它是一种病毒因子,对于在有性周期中病毒 DNA 复制后晚期基因转录的激活至关重要。为了研究 BcRF1 蛋白的功能,我们构建了一种缺失该基因的重组 EBV。在 HEK293 细胞中,这种重组病毒在有性周期中正常进行 DNA 复制,但不能高水平表达晚期基因转录物或蛋白质,导致非生产性感染。有趣的是,大多数 EBV 晚期基因的启动子中都存在一个 TATT 基序,位于 TATA 盒的位置。我们在这里表明,BcRF1 与 TATT 基序形成复合物,这种相互作用对于晚期病毒基因表达的激活是必需的。此外,我们的结果表明,BcRF1 通过与其他病毒蛋白的相互作用发挥作用。