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A NOVEL PRD I AND TG BINDING ACTIVITY INVOLVED IN VIRUS-INDUCED TRANSCRIPTION OF IFN-A GENES

机译:病毒诱导的IFN-A基因转录中PRD I和TG结合的新活性

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摘要

Comparative analysis of the inducible elements of the mouse interferon A4 and A11 gene promoters (IE-A4 and IE-A11) by transient transfection experiments, DNase I footprinting and electrophoretic mobility shift assays resulted in identification of a virus-induced binding activity suggested to be involved in NBV-induced activation of transcription of these genes, The virus-induced factor, termed VIF, is activated early by contact of virions with cells, It specifically recognizes the PRD I-like domain shared by both inducible elements, as well as the TO-like domain of IE-A4, This factor, distinct from the IRF-1, IRF-2 and the alpha F1 binding proteins and presenting a different affinity pattern from that of the TG protein, is proposed as a candidate for IFN-type I gene regulation.
机译:通过瞬时转染实验,DNase I足迹和电泳迁移率变动分析对小鼠干扰素A4和A11基因启动子(IE-A4和IE-A11)的诱导因子进行比较分析,结果表明鉴定出病毒诱导的结合活性是与NBV诱导的这些基因的转录激活有关,病毒诱导的因子称为VIF,是通过病毒体与细胞的接触而被早期激活的。它特异性地识别了两种诱导因子以及与之相关的PRD I样结构域。提议将IE-A4的TO样结构域与IRF-1,IRF-2和αF1结合蛋白区分开,并呈现与TG蛋白不同的亲和力模式,作为IFN-型候选物。我基因调控。

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