Aubry Valentin, Mure Fabrice, Mariamé Bernard, Deschamps Thibaut, Wyrwicz Lucjan S, Manet Evelyne, Gruffat Henri
CIRI, Centre International de Recherche en Infectiologie, Oncogenic Herpesviruses Team, Université de Lyon, Lyon, France INSERM, U1111, Lyon, France Ecole Normale Supérieure de Lyon, Lyon, France Université Lyon 1, Centre International de Recherche en Infectiologie, Lyon, France CNRS, UMR5308, Lyon, France.
CNRS, UMR 5099-LBME (Laboratoire de Biologie Moléculaire des Eucaryotes), USR 3505-ITAV (Institut des Technologies Avancées des Sciences du Vivant), Toulouse, France.
J Virol. 2014 Nov;88(21):12825-38. doi: 10.1128/JVI.02139-14. Epub 2014 Aug 27.
During their productive cycle, herpesviruses exhibit a strictly regulated temporal cascade of gene expression that has three general stages: immediate early (IE), early (E), and late (L). Promoter complexity differs strikingly between IE/E genes and L genes. IE and E promoters contain cis-regulating sequences upstream of a TATA box, whereas L promoters comprise a unique cis element. In the case of the gammaherpesviruses, this element is usually a TATT motif found in the position where the consensus TATA box of eukaryotic promoters is typically found. Epstein-Barr virus (EBV) encodes a protein, called BcRF1, which has structural homology with the TATA-binding protein and interacts specifically with the TATT box. However, although necessary for the expression of the L genes, BcRF1 is not sufficient, suggesting that other viral proteins are also required. Here, we present the identification and characterization of a viral protein complex necessary and sufficient for the expression of the late viral genes. This viral complex is composed of five different proteins in addition to BcRF1 and interacts with cellular RNA polymerase II. During the viral productive cycle, this complex, which we call the vPIC (for viral preinitiation complex), works in concert with the viral DNA replication machinery to activate expression of the late viral genes. The EBV vPIC components have homologs in beta- and gammaherpesviruses but not in alphaherpesviruses. Our results not only reveal that beta- and gammaherpesviruses encode their own transcription preinitiation complex responsible for the expression of the late viral genes but also indicate the close evolutionary history of these viruses.
Control of late gene transcription in DNA viruses is a major unsolved question in virology. In eukaryotes, the first step in transcriptional activation is the formation of a permissive chromatin, which allows assembly of the preinitiation complex (PIC) at the core promoter. Fixation of the TATA box-binding protein (TBP) is a key rate-limiting step in this process. This study provides evidence that EBV encodes a complex composed of six proteins necessary for the expression of the late viral genes. This complex is formed around a viral TBP-like protein and interacts with cellular RNA polymerase II, suggesting that it is directly involved in the assembly of a virus-specific PIC (vPIC).
在其生产周期中,疱疹病毒呈现出严格调控的基因表达时间级联,分为三个一般阶段:立即早期(IE)、早期(E)和晚期(L)。IE/E基因和L基因的启动子复杂性存在显著差异。IE和E启动子在TATA框上游包含顺式调控序列,而L启动子包含一个独特的顺式元件。对于γ疱疹病毒而言,该元件通常是一个TATT基序,位于真核启动子的共有TATA框通常所在的位置。爱泼斯坦 - 巴尔病毒(EBV)编码一种名为BcRF1的蛋白质,它与TATA结合蛋白具有结构同源性,并与TATT框特异性相互作用。然而,尽管BcRF1对L基因的表达是必需的,但并不充分,这表明还需要其他病毒蛋白。在这里,我们展示了一种对晚期病毒基因表达既必要又充分的病毒蛋白复合物的鉴定和特征。除了BcRF1之外,这种病毒复合物由五种不同的蛋白质组成,并与细胞RNA聚合酶II相互作用。在病毒生产周期中,我们将这种复合物称为vPIC(病毒预起始复合物),它与病毒DNA复制机制协同作用以激活晚期病毒基因的表达。EBV vPIC的成分在β和γ疱疹病毒中有同源物,但在α疱疹病毒中没有。我们的结果不仅揭示了β和γ疱疹病毒编码它们自己的负责晚期病毒基因表达的转录预起始复合物,还表明了这些病毒密切的进化史。
DNA病毒中晚期基因转录的控制是病毒学中一个主要未解决的问题。在真核生物中,转录激活的第一步是形成允许的染色质,这允许在核心启动子处组装预起始复合物(PIC)。TATA框结合蛋白(TBP)的固定是这个过程中的关键限速步骤。这项研究提供了证据,表明EBV编码一种由六种蛋白质组成的复合物,对晚期病毒基因的表达是必需的。这种复合物围绕一种病毒TBP样蛋白形成,并与细胞RNA聚合酶II相互作用,表明它直接参与病毒特异性PIC(vPIC)的组装。