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Identification and characterization of G-quadruplex formation within the EP0 promoter of pseudorabies virus

机译:伪狂犬病病毒EP0启动子中G四联体形成的鉴定和表征

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摘要

EP0 is an important early gene that modulates the life cycle of pseudorabies virus (PRV). A guanine-rich sequence overlapping with three Sp1 binding sites is located upstream of the transcription start site (TSS) in the EP0 promoter. Using native polyacrylamide gel electrophoresis (PAGE) and circular dichroism (CD), we verified that the G-rich region in the EP0 promoter forms an intramolecular parallel G-quadruplex (G4) in the presence of K+ ions. Further dimethyl sulphate (DMS) footprinting and Taq polymerase stop assays indicates the potential polymorphic folding of G4. In addition, a small chemical ligand, pyridostatin (PDS), promotes and stabilizes the formation of G4. Interestingly, based on the results of electrophoretic mobility shift assays (EMSA), the Sp1 protein bound to G4-bearing DNA with more affinity than DNA lacking the G4 structure. According to the luciferase reporter assay, G4 negatively regulates the EP0 promoter activity. These results demonstrate that Sp1 and G4 cooperate to regulate EP0 promoter activity.
机译:EP0是调节伪狂犬病病毒(PRV)生命周期的重要早期基因。与三个Sp1结合位点重叠的富含鸟嘌呤的序列位于EP0启动子中转录起始位点(TSS)的上游。使用天然聚丙烯酰胺凝胶电泳(PAGE)和圆二色性(CD),我们验证了在存在K + 的情况下,EP0启动子中富含G的区域形成了分子内平行G-四链体(G4)。离子。进一步的硫酸二甲酯(DMS)足迹和Taq聚合酶终止试验表明了G4的潜在多态性折叠。另外,一种小的化学配体,吡ido他汀(PDS),可促进并稳定G4的形成。有趣的是,基于电泳迁移率变动分析(EMSA)的结果,Sp1蛋白与带有G4的DNA结合的亲和力比缺乏G4结构的DNA更高。根据荧光素酶报告基因测定,G4负调节EP0启动子活性。这些结果表明,Sp1和G4共同调节EP0启动子的活性。

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