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Colocalization of Interferon Regulatory Factor 7 (IRF7) with Latent Membrane Protein 1 (LMP1) of Epstein-Barr Virus

机译:干扰素调节因子7(IRF7)与爱泼斯坦-巴尔病毒的潜在膜蛋白1(LMP1)的共定位

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摘要

Interferon regulatory factor 7 (IRF7) is one of the transcriptional factors for the activation of type I Interferon (IFN) genes. It is known that IRF7 and the latent membrane protein 1 (LMP1) of Epstein-Barr virus (EBV) are highly expressed in EBV type III latency cells, and LMP1 induces mRNA expression of IRF7. In this study, the expression pattern of endogenous IRF7 was observed in several B cell lines with or without EBV infection by immunofluorescence staining. IRF7 was localized in the cytoplasm of EBV-negative B cells and EBV type I latency B cell lines. However, IRF7 was located both in the cytoplasm and nucleus of EBV type III latency cell lines. In the Jijoye cell (type III latency cell), IRF7 was colocalized with LMP1 in the cytoplasm in a capping configuration, and their interaction was confirmed by co-immunoprecipitation of LMP1 and IRF7. This colocalization was confirmed by co-transfection of IRF7 and LMP1 plasmids in EBV-negative B cells. These results suggest that the IRF7 and LMP1 interact with each other, and this may relate to the mechanism whereby LMP1 exerts functional effects in B-lymphocytes.
机译:干扰素调节因子7(IRF7)是激活I型干扰素(IFN)基因的转录因子之一。众所周知,爱泼斯坦-巴尔病毒(EBV)的IRF7和潜伏膜蛋白1(LMP1)在EBV III型潜伏期细胞中高度表达,LMP1诱导IRF7的mRNA表达。在这项研究中,通过免疫荧光染色在带有或不带有EBV感染的几种B细胞系中观察到了内源性IRF7的表达模式。 IRF7位于EBV阴性B细胞和EBV I型潜伏期B细胞系的细胞质中。但是,IRF7位于EBV III型潜伏期细胞系的细胞质和细胞核中。在Jijoye细胞(III型潜伏期细胞)中,IRF7与LMP1在细胞质中处于定位状态,并且处于封闭状态,并且通过LMP1和IRF7的共免疫沉淀来确认它们的相互作用。通过在EBV阴性B细胞中共转染IRF7和LMP1质粒,证实了这种共定位。这些结果表明IRF7和LMP1相互作用,这可能与LMP1在B淋巴细胞发挥功能作用的机制有关。

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