Chau Charles M, Lieberman Paul M
The Wistar Institute, 3601 Spruce Street, Philadelphia, PA 19104, USA.
J Virol. 2004 Nov;78(22):12308-19. doi: 10.1128/JVI.78.22.12308-12319.2004.
The oncogenic potential of latent Epstein-Barr virus (EBV) can be regulated by epigenetic factors controlling LMP1 and EBNA2 gene transcription. The EBV latency control region (LCR) constitutes approximately 12 kb of viral sequence spanning the divergent promoters of LMP1 and EBNA2 and encompasses the EBV latent replication origin OriP and RNA polymerase III-transcribed EBV-encoded RNA genes. We have used the chromatin immunoprecipitation assay to examine the chromatin architecture of the LCR in different types of EBV latency programs. We have found that histone H3 K4 methylation (H3mK4) was enriched throughout a large domain that extended from internal repeat 1 (IR1) to the terminal repeat in type III latency where EBNA2 and LMP1 genes are expressed. In type I latency where EBNA2 and LMP1 genes are transcriptionally silent, the H3mK4 domain contracts and does not enter the EBNA2 or LMP1 promoters. In contrast, histone H3 K9 methylation (H3mK9), associated with silent heterochromatin, was enriched in the EBNA2 and LMP1 upstream control regions in type I but not type III cells. MTA [5'-deoxy-5'(methylthio)adenosine], a pharmacological inhibitor of protein methylation, globally reduced histone H3mK4 and inhibited EBNA2 transcription in type III cells. 5'-Azacytidine, an inhibitor of DNA methylation that derepresses EBNA2 transcription in type I latency, caused H3mK4 expansion and a corresponding loss of H3mK9 at IR1. The chromatin boundary protein and transcription repressor CCCTC-binding factor was enriched at the EBNA2 transcription control region in type I but not type III cells. We also present evidence that OriP binding factors EBNA1 and ORC2 can interact with sequences outside of OriP including a region within IR1 that may influence EBNA2 transcription status. These results indicate that types I and III latency programs have distinct histone methylation patterns in the LCR and suggest that chromatin architecture coordinates gene expression of LMP1 and EBNA2.
潜伏性爱泼斯坦-巴尔病毒(EBV)的致癌潜力可由控制LMP1和EBNA2基因转录的表观遗传因素调节。EBV潜伏控制区(LCR)由约12 kb的病毒序列组成,跨越LMP1和EBNA2的不同启动子,包含EBV潜伏复制起点OriP和RNA聚合酶III转录的EBV编码RNA基因。我们利用染色质免疫沉淀试验检测了不同类型EBV潜伏程序中LCR的染色质结构。我们发现,在III型潜伏中,组蛋白H3 K4甲基化(H3mK4)在从内部重复序列1(IR1)延伸至末端重复序列的大区域内富集,此时EBNA2和LMP1基因表达。在I型潜伏中,EBNA2和LMP1基因转录沉默,H3mK4结构域收缩,不进入EBNA2或LMP1启动子。相反,与沉默异染色质相关的组蛋白H3 K9甲基化(H3mK9)在I型而非III型细胞的EBNA2和LMP1上游控制区富集。MTA[5'-脱氧-5'(甲硫基)腺苷],一种蛋白质甲基化的药理学抑制剂,在III型细胞中整体降低组蛋白H3mK4并抑制EBNA2转录。5'-氮杂胞苷,一种DNA甲基化抑制剂,可在I型潜伏中解除对EBNA2转录的抑制,导致H3mK4扩展以及IR1处H3mK9相应减少。染色质边界蛋白和转录抑制因子CCCTC结合因子在I型而非III型细胞的EBNA2转录控制区富集。我们还提供证据表明,OriP结合因子EBNA1和ORC2可与OriP以外的序列相互作用,包括IR1内可能影响EBNA2转录状态的区域。这些结果表明,I型和III型潜伏程序在LCR中具有不同的组蛋白甲基化模式,并提示染色质结构协调LMP1和EBNA2的基因表达。