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Regulation of Human Polyomavirus JC Virus Gene Transcription by AP-1 in Glial Cells

机译:AP-1在胶质细胞中对人多瘤病毒JC病毒基因转录的调控

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摘要

The activating transcription factor 1 (AP-1) family of proteins consists of a large number of inducible factors that are implicated in many biological processes, including cellular and viral gene expression, cell proliferation, differentiation, and tumorigenesis. Here, we investigated the role of the AP-1 family members c-Jun and c-Fos in transcriptional regulation of the JC virus (JCV) promoter in glial cells. DNA binding studies demonstrated the specific association of c-Jun with its DNA sequences corresponding to the AP-1 site within the JCV promoter. Functional analysis of the promoter showed that ectopic expression of c-Jun and c-Fos results in an additive activation of the JCV early and late promoters. Further functional assays indicated that the JCV AP-1 binding site is sufficient to confer responsiveness to both c-Jun/c-Fos- and UV-induced activation when transposed to a heterologous promoter. Analysis of c-Jun expression during the viral infection cycle by Western blotting revealed that c-Jun is posttranslationally modified by phosphorylation and its protein level is substantially increased at the late phases of infection cycle. Altogether, our findings indicate that AP-1 family members may play a role in the pathogenesis of JCV-induced disease in the human brain by modulating JCV gene transcription.
机译:蛋白质的激活转录因子1(AP-1)家族由许多诱导性因子组成,这些因子与许多生物学过程有关,包括细胞和病毒基因表达,细胞增殖,分化和肿瘤发生。在这里,我们调查了AP-1家族成员c-Jun和c-Fos在神经胶质细胞JC病毒(JCV)启动子的转录调控中的作用。 DNA结合研究表明c-Jun与它对应于JCV启动子内AP-1位点的DNA序列有特定的联系。启动子的功能分析表明,c-Jun和c-Fos的异位表达导致JCV早期和晚期启动子的加性激活。进一步的功能分析表明,JCV AP-1结合位点在转位至异源启动子时足以赋予对c-Jun / c-Fos-和UV诱导的激活的响应性。通过蛋白质印迹分析病毒感染周期中c-Jun的表达表明,c-Jun在磷酸化后被翻译后修饰,其蛋白水平在感染周期的后期显着增加。总之,我们的发现表明AP-1家族成员可能通过调节JCV基因转录在人脑JCV诱发疾病的发病机理中发挥作用。

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