Department of Dermatology, University of California, Davis, School of Medicine, Sacramento, California, USA.
J Virol. 2013 Jun;87(12):6782-93. doi: 10.1128/JVI.00011-13. Epub 2013 Apr 10.
Kaposi's sarcoma-associated herpesvirus (KSHV) latent genomes are tethered to host histones to form a minichromosome also known as an "episome." Histones, which are core components of chromatin, are heavily modified by various histone-targeting enzymes. Posttranslational modifications of histones significantly influence accessibility of transcriptional factors and thus have profound effects on gene expression. Recent studies showed that epigenetic marks on the KSHV episome are well organized, exemplified by the absence of histone H3 lysine 9 (H3K9) methylation, a heterochromatic histone mark, from immediate early and latent gene promoters in naturally infected cells. The present study revealed a mechanistic insight into KSHV epigenome regulation via a complex consisting of LANA and the H3K9me1/2 histone demethylase JMJD1A/KDM3A. This complex was isolated from HeLa cell nuclear extracts stably expressing LANA and was verified by coimmunoprecipitation analyses and with purified proteins. LANA recruitment sites on the KSHV genome inversely correlated with H3K9me2 histone marks in naturally infected cells, and methylation of H3K9 significantly inhibited LANA binding to the histone H3 tail. Chromatin immunoprecipitation coupled with KSHV tiling arrays identified the recruitment sites of the complex, while depletion of LANA expression or overexpression of a KDM3A binding-deficient mutant decreased KDM3A recruitment to the KSHV genome. Finally, ablation of KDM3A expression from latently KSHV-infected cells significantly inhibited KSHV gene expression, leading to decreased KSHV replication during reactivation. Taken together, our results suggest that LANA may play a role in regulation of epigenetic marks on the KSHV genome, which is in part through association with the histone demethylase KDM3A.
卡波西肉瘤相关疱疹病毒(KSHV)潜伏基因组与宿主组蛋白相连,形成一个被称为“附加体”的微染色体。组蛋白是染色质的核心成分,被各种组蛋白靶向酶进行了大量修饰。组蛋白的翻译后修饰显著影响转录因子的可及性,因此对基因表达有深远影响。最近的研究表明,KSHV 附加体上的表观遗传标记组织良好,例如在天然感染细胞中,早期和潜伏基因启动子上没有组蛋白 H3 赖氨酸 9(H3K9)甲基化,这是一种异染色质组蛋白标记。本研究通过包含 LANA 和 H3K9me1/2 组蛋白去甲基酶 JMJD1A/KDM3A 的复合物,揭示了 KSHV 表观基因组调控的机制。该复合物从稳定表达 LANA 的 HeLa 细胞核提取物中分离出来,并通过共免疫沉淀分析和纯化蛋白进行了验证。KSHV 基因组上 LANA 的募集位点与天然感染细胞中 H3K9me2 组蛋白标记呈负相关,并且 H3K9 的甲基化显著抑制了 LANA 与组蛋白 H3 尾部的结合。与 KSHV 平铺阵列相结合的染色质免疫沉淀鉴定了复合物的募集位点,而 LANA 表达的缺失或 KDM3A 结合缺陷突变体的过表达会降低 KDM3A 对 KSHV 基因组的募集。最后,潜伏感染 KSHV 的细胞中 KDM3A 的表达缺失显著抑制了 KSHV 基因的表达,导致在重新激活时 KSHV 复制减少。总之,我们的结果表明,LANA 可能在 KSHV 基因组上的表观遗传标记的调节中发挥作用,部分是通过与组蛋白去甲基酶 KDM3A 相关联来实现的。