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乳头瘤病毒E2蛋白与Brm染色质重塑复合物的相互作用导致转录激活增强。

Interaction of papillomavirus E2 protein with the Brm chromatin remodeling complex leads to enhanced transcriptional activation.

作者信息

Kumar R Ajay, Naidu Samisubbu R, Wang Xiaoyu, Imbalzano Anthony N, Androphy Elliot J

机构信息

Department of Medicine, University of Massachusetts Medical School, 364 Plantation Street, LRB 327, Worcester, MA 01605, USA.

出版信息

J Virol. 2007 Mar;81(5):2213-20. doi: 10.1128/JVI.01746-06. Epub 2006 Dec 6.

Abstract

Papillomavirus E2 is a sequence-specific DNA binding protein that regulates transcription and replication of the viral genome. The transcriptional activities of E2 are typically evaluated by transient transfection of nonreplicating E2-dependent reporters. We sought to address whether E2 activates transcription in an episomal context and its potential interaction with the chromatin remodeling proteins. Using an Epstein-Barr virus-based episomal reporter, we demonstrate that E2 stimulates transcription from an E2-dependent promoter in a chromatin context. This activation is enhanced by the presence of proteins associated with SWI/SNF complexes, which are ATP-dependent chromatin remodeling enzymes. We show that exogenous expression of the Brm ATPase enhances E2 activity in SWI/SNF-deficient cell lines and that the amino-terminal transactivation domain of E2 mediates association with the Brm complex in vivo. Using chromatin immunoprecipitation assays, we demonstrate that Brm enhances promoter occupancy by E2 in an episomal context. Our results demonstrate that E2 activates transcription from an episomal reporter system and reveal a novel property of E2 in collaborating with the Brm chromatin remodeling complex in enhancing transcriptional activation.

摘要

乳头瘤病毒E2是一种序列特异性DNA结合蛋白,可调节病毒基因组的转录和复制。E2的转录活性通常通过非复制型E2依赖性报告基因的瞬时转染来评估。我们试图探讨E2在附加体环境中是否激活转录及其与染色质重塑蛋白的潜在相互作用。使用基于爱泼斯坦-巴尔病毒的附加体报告基因,我们证明E2在染色质环境中刺激来自E2依赖性启动子的转录。与SWI/SNF复合物相关的蛋白质(即ATP依赖性染色质重塑酶)的存在增强了这种激活作用。我们表明,Brm ATP酶的外源性表达增强了SWI/SNF缺陷细胞系中的E2活性,并且E2的氨基末端反式激活结构域在体内介导与Brm复合物的结合。使用染色质免疫沉淀分析,我们证明Brm在附加体环境中增强了E2对启动子的占据。我们的结果表明,E2从附加体报告系统激活转录,并揭示了E2在与Brm染色质重塑复合物协同增强转录激活方面的新特性。

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