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人巨细胞病毒天然和实验潜伏模型中潜伏病毒基因表达的分析及其与潜伏启动子处组蛋白修饰的相关性。

Analysis of latent viral gene expression in natural and experimental latency models of human cytomegalovirus and its correlation with histone modifications at a latent promoter.

机构信息

Department of Medicine, University of Cambridge, Addenbrooke's Hospital, Cambridge CB2 2QQ, UK.

出版信息

J Gen Virol. 2010 Mar;91(Pt 3):599-604. doi: 10.1099/vir.0.015602-0. Epub 2009 Nov 11.

DOI:10.1099/vir.0.015602-0
PMID:19906945
Abstract

Human cytomegalovirus (HCMV) is an opportunistic human pathogen that establishes a lifelong latent infection, which can reactivate periodically. If unchecked by a robust immune response, this reactivation can result in severe disease in immunocompromised patients. Reactivation of latent virus in myeloid progenitor cells is concomitant with cellular differentiation through regulation of the major immediate-early promoter (MIEP) by chromatin remodelling. In this study, we analysed the expression of the latent gene transcript UL81-82as (LUNA). LUNA is expressed in latently infected CD34(+) cells and its expression decreases as CD34(+) cells differentiate to immature dendritic cells. Upon maturation (and HCMV reactivation), a second wave of transcription occurs, consistent with expression during lytic infection. Furthermore, we show that the LUNA promoter is associated with acetylated histones during HCMV latency in experimentally and naturally infected CD34(+) cells, thus suggesting that latent gene promoters are, like the MIEP, regulated by post-translational modifications of their associated histone proteins.

摘要

人类巨细胞病毒(HCMV)是一种机会性人类病原体,可建立终身潜伏感染,这种感染可周期性地重新激活。如果未被强大的免疫反应所遏制,这种重新激活可能会导致免疫功能低下的患者发生严重疾病。潜伏病毒在髓系祖细胞中的重新激活伴随着细胞分化,这是通过染色质重塑对主要即刻早期启动子(MIEP)的调节来实现的。在这项研究中,我们分析了潜伏基因转录本 UL81-82as(LUNA)的表达。LUNA 在潜伏感染的 CD34+细胞中表达,并且随着 CD34+细胞分化为未成熟树突状细胞,其表达水平降低。在成熟(和 HCMV 重新激活)时,会发生第二波转录,与裂解感染期间的表达一致。此外,我们表明,在实验和自然感染的 CD34+细胞中,LUNA 启动子与潜伏期间的乙酰化组蛋白相关,因此表明潜伏基因启动子与 MIEP 一样,受其相关组蛋白蛋白的翻译后修饰调节。

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