Department of Systems Biotechnology, Chung-Ang University, Anseong, Korea.
Institute of Molecular Biology, University of Oregon, Eugene, OR, 97403, USA.
Nat Commun. 2020 Feb 13;11(1):877. doi: 10.1038/s41467-019-14152-8.
Epstein-Barr virus (EBV) genomes persist in latently infected cells as extrachromosomal episomes that attach to host chromosomes through the tethering functions of EBNA1, a viral encoded sequence-specific DNA binding protein. Here we employ circular chromosome conformation capture (4C) analysis to identify genome-wide associations between EBV episomes and host chromosomes. We find that EBV episomes in Burkitt's lymphoma cells preferentially associate with cellular genomic sites containing EBNA1 binding sites enriched with B-cell factors EBF1 and RBP-jK, the repressive histone mark H3K9me3, and AT-rich flanking sequence. These attachment sites correspond to transcriptionally silenced genes with GO enrichment for neuronal function and protein kinase A pathways. Depletion of EBNA1 leads to a transcriptional de-repression of silenced genes and reduction in H3K9me3. EBV attachment sites in lymphoblastoid cells with different latency type show different correlations, suggesting that host chromosome attachment sites are functionally linked to latency type gene expression programs.
EB 病毒(EBV)基因组作为附加体以染色体外形式存在于潜伏感染的细胞中,通过 EBNA1 的连接功能附着在宿主染色体上,EBNA1 是一种病毒编码的序列特异性 DNA 结合蛋白。在这里,我们采用环状染色体构象捕获(4C)分析来鉴定 EBV 附加体与宿主染色体之间的全基因组关联。我们发现,伯基特淋巴瘤细胞中的 EBV 附加体优先与包含 EBNA1 结合位点的细胞基因组位点结合,这些位点富含 B 细胞因子 EBF1 和 RBP-jK、抑制性组蛋白标记 H3K9me3 和富含 A/T 的侧翼序列。这些附着位点与转录沉默基因相对应,GO 富集分析表明这些基因具有神经元功能和蛋白激酶 A 途径的特征。EBNA1 的缺失导致沉默基因的转录去抑制和 H3K9me3 的减少。具有不同潜伏类型的淋巴母细胞系中的 EBV 附着位点显示出不同的相关性,这表明宿主染色体附着位点与潜伏类型基因表达程序在功能上相关。