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E1和E2蛋白与牛乳头瘤病毒复制起点的结合。

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

作者信息

Sedman T, Sedman J, Stenlund A

机构信息

Cold Spring Harbor Laboratory, New York 11724, USA.

出版信息

J Virol. 1997 Apr;71(4):2887-96. doi: 10.1128/JVI.71.4.2887-2896.1997.

Abstract

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.

摘要

牛乳头瘤病毒(BPV)的DNA复制需要由E1和E2开放阅读框编码的两种病毒蛋白。E1和E2是序列特异性DNA结合蛋白,它们与BPV复制起点(ori)中的同源结合位点结合。E1和E2蛋白可以相互发生物理作用,当两种蛋白的结合位点都存在时,这种相互作用会导致协同结合。我们使用DNA酶I足迹分析、凝胶迁移率变动分析和干涉分析,分析了在不存在和存在E2的情况下E1与ori的结合情况。我们还在E1结合位点产生了大量点突变,并测试了它们与E1的结合情况以及在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以不同形式与ori结合,并且E2对E1的结合具有定量和定性影响。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,并且在存在和不存在E2的情况下,这些识别序列的不同子集用于E1的结合。

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