首页> 美国卫生研究院文献>Journal of Virology >Interferon Regulatory Factor 5 Represses Expression of the Epstein-Barr Virus Oncoprotein LMP1: Braking of the IRF7/LMP1 Regulatory Circuit
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Interferon Regulatory Factor 5 Represses Expression of the Epstein-Barr Virus Oncoprotein LMP1: Braking of the IRF7/LMP1 Regulatory Circuit

机译: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:IRF7 / LMP1调节电路的制动

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摘要

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.
机译:我们已经报道了干扰素调节因子7(IRF7)和爱泼斯坦-巴尔病毒(EBV)癌蛋白1(LMP1)之间存在正调节回路的证据(S. Ning,AM Hahn和JS Pagano,J.Virol。77:9359 -9368,2003)。为了探索该电路的可能制动机制,分析了几种II型EBV感染的细胞系,它们表达不同水平的LMP1和IRF7蛋白,因此便于研究LMP1表达的调节。 IRF7和LMP1的内源性水平直接相关。 IRF7显性负突变体的瞬时表达降低了LMP1水平。内源性IRF5和IRF7蛋白在EBV阳性细胞中表现出物理结合。 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显性阴性构建体或IRF5小干扰RNA会导致内源性LMP1水平升高。这些结果表明,IRF5最有可能通过与IRF7相互作用而下调IRF7对LMP1表达的诱导,并提供一种调节IRF7与LMP1之间调节电路的手段。

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