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A novel PRD I and TG binding activity involved in virus-induced transcription of IFN-A genes.

机译:新型的PRD I和TG结合活性参与病毒诱导的IFN-A基因转录。

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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 1 footprinting and electrophoretic mobility shift assays resulted in identification of a virus-induced binding activity suggested to be involved in NDV-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 TG-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 1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参与NDV诱导的这些基因转录激活。病毒诱导的因子称为VIF,可通过病毒体与细胞的接触而被早期激活。它专门识别可诱导元件共享的PRD I样结构域,以及IE-A4的TG样结构域。该因子不同于IRF-1,IRF-2和αF1结合蛋白,并且呈现出与TG蛋白不同的亲和力模式,被提议作为IFN-I型基因调控的候选者。

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