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Simian virus 40 (SV40) DNA replication: SV40 large T antigen unwinds DNA containing the SV40 origin of replication.

机译:猿猴病毒40(SV40)DNA复制:SV40大T抗原解链包含SV40复制起点的DNA。

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摘要

The simian virus 40 (SV40) large T antigen (large tumor antigen), in conjunction with a topoisomerase, a DNA binding protein, and ATP, catalyzed the conversion of a circular duplex DNA molecule containing the SV40 origin of replication to a form with unusual electrophoretic mobility that we have named form U. Analysis of this molecule revealed it to be a highly underwound covalently closed circle. DNA unwinding was not detected with DNA containing a SV40 T-antigen binding site II mutation that renders the DNA inactive in replication. The unwinding reaction requires the action of a helicase, and SV40 T-antigen preparations contain such an activity. The T-antigen-associated ability to unwind DNA copurified with other activities intrinsic to T antigen [ability to support replication of SV40 DNA containing the SV40 origin, poly(dT)-stimulated ATPase activity, and DNA helicase]. However, in contrast to the unwinding activity, the SV40 T-antigen-associated helicase activity was not sequence-specific. A variety of labeled oligonucleotides hybridized with circular single-stranded DNA were displaced by T antigen in the presence of ATP.
机译:猿猴病毒40(SV40)大T抗原(大肿瘤抗原)与拓扑异构酶,DNA结合蛋白和ATP一起催化了包含SV40复制起点的环状双链DNA分子转化为异常形式电泳迁移率,我们已命名为U。对该分子的分析表明,它是一个高度未加共价共价闭合的圆圈。含有SV40 T抗原结合位点II突变的DNA未检测到DNA释放,该突变使DNA不能复制。解开反应需要解旋酶的作用,并且SV40 T-抗原制剂具有这种活性。与T抗原相关的解开DNA的能力与T抗原固有的其他活性共纯化[支持包含SV40起源的SV40 DNA复制,poly(dT)刺激的ATPase活性和DNA解旋酶的复制能力]。然而,与展开活性相反,SV40 T-抗原相关的解旋酶活性不是序列特异性的。在ATP存在下,多种与环状单链DNA杂交的标记寡核苷酸被T抗原取代。

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