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Binding of the E1 and E2 proteins to the origin of replication of bovine papillomavirus.

机译:E1和E2蛋白与牛乳头瘤病毒复制起点的结合。

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摘要

DNA replication of bovine papillomavirus (BPV) requires two viral proteins encoded from the E1 and E2 open reading frames. E1 and E2 are sequence-specific DNA binding proteins that bind to their cognate binding sites in the BPV origin of replication (ori). The E1 and E2 proteins can interact physically with each other, and this interaction results in cooperative binding when binding sites for both proteins are present. We have analyzed the binding of E1 to the ori in the absence and presence of E2, using DNase I footprint analysis, gel mobility shift assays, and interference analysis. We have also generated a large number of point mutations in the E1 binding site and tested them for binding of E1 as well as for activity in DNA replication. Our results demonstrate that E1 binds to the ori in different forms in the absence and presence of E2 and that E2 has both a quantitative and a qualitative effect on the binding of E1. Our results also suggest that the ori contains multiple overlapping individual E1 recognition sequences which together constitute the E1 binding site and that different subsets of these recognition sequences are used for binding of E1 in the presence and absence of E2.
机译:牛乳头瘤病毒(BPV)的DNA复制需要从E1和E2开放阅读框编码的两种病毒蛋白。 E1和E2是与BPV复制起点(ori)中其同源结合位点结合的序列特异性DNA结合蛋白。 E1和E2蛋白可以彼此物理相互作用,并且当存在两种蛋白的结合位点时,这种相互作用会导致协同结合。我们已经使用DNase I足迹分析,凝胶迁移率移动分析和干扰分析在E2不存在和存在的情况下分析了E1与ori的结合。我们还在E1结合位点产生了大量的点突变,并测试了它们与E1的结合以及DNA复制中的活性。我们的结果表明,在不存在和存在E2的情况下,E1以不同的形式与ori结合,并且E2对E1的结合具有定量和定性作用。我们的结果还表明,ori包含多个重叠的单个E1识别序列,这些序列共同构成E1结合位点,并且这些识别序列的不同子集用于在存在和不存在E2的情况下结合E1。

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