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本文引用的文献

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Hyperphosphorylation of EBNA2 by Epstein-Barr virus protein kinase suppresses transactivation of the LMP1 promoter.爱泼斯坦-巴尔病毒蛋白激酶对EBNA2的过度磷酸化抑制了LMP1启动子的反式激活。
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Interferon regulatory factor 7 is associated with Epstein-Barr virus-transformed central nervous system lymphoma and has oncogenic properties.干扰素调节因子7与爱泼斯坦-巴尔病毒转化的中枢神经系统淋巴瘤相关,并具有致癌特性。
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干扰素调节因子5抑制爱泼斯坦-巴尔病毒癌蛋白LMP1的表达:对IRF7/LMP1调节回路的抑制作用

Interferon regulatory factor 5 represses expression of the Epstein-Barr virus oncoprotein LMP1: braking of the IRF7/LMP1 regulatory circuit.

作者信息

Ning Shunbin, Huye Leslie E, Pagano Joseph S

机构信息

Lineberger Comprehensive Cancer Center, University of North Carolina, School of Medicine, Campus Box 7295, Chapel Hill, NC 27599, USA.

出版信息

J Virol. 2005 Sep;79(18):11671-6. doi: 10.1128/JVI.79.18.11671-11676.2005.

DOI:10.1128/JVI.79.18.11671-11676.2005
PMID:16140744
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1212628/
Abstract

We have reported evidence for a positive regulatory circuit between interferon regulatory factor 7 (IRF7) and the Epstein-Barr virus (EBV) oncoprotein 1 (LMP1) (S. Ning, A. M. Hahn, and J. S. Pagano, J. Virol. 77:9359-9368, 2003). To explore a possible braking mechanism for this circuit, several type II EBV-infected cell lines that express different levels of LMP1 and IRF7 proteins and therefore are convenient for studying modulation of expression of LMP1 were analyzed. Endogenous levels of IRF7 and LMP1 were directly correlated. Transient expression of an IRF7 dominant-negative mutant decreased LMP1 levels. Endogenous IRF5 and IRF7 proteins were shown to physically associate in EBV-positive cells. Transient expression of IRF5 decreased activation of the LMP1 promoter by IRF7 in a dose-dependent manner. Finally, transfection of either an IRF5 dominant-negative construct or IRF5 small interfering RNA in these cells resulted in increases in endogenous levels of LMP1. These results indicate that IRF5 can downregulate IRF7's induction of expression of LMP1 most likely by interacting with IRF7 and provide a means of modulating a regulatory circuit between IRF7 and LMP1.

摘要

我们已报道了干扰素调节因子7(IRF7)与爱泼斯坦-巴尔病毒(EBV)癌蛋白1(LMP1)之间存在正向调节回路的证据(S.宁、A.M.哈恩和J.S.帕加诺,《病毒学杂志》77:9359 - 9368,2003年)。为探究该回路可能的制动机制,我们分析了几种II型EBV感染的细胞系,这些细胞系表达不同水平的LMP1和IRF7蛋白,因此便于研究LMP1表达的调控。IRF7和LMP1的内源性水平直接相关。IRF7显性负性突变体的瞬时表达降低了LMP1水平。在EBV阳性细胞中,内源性IRF5和IRF7蛋白显示出物理性结合。IRF5的瞬时表达以剂量依赖的方式降低了IRF7对LMP1启动子的激活。最后,在这些细胞中转染IRF5显性负性构建体或IRF5小干扰RNA导致LMP1内源性水平升高。这些结果表明,IRF5最有可能通过与IRF7相互作用来下调IRF7对LMP1表达的诱导,并提供了一种调节IRF7与LMP1之间调节回路的方法。