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小鼠p53蛋白通过抑制SV40大T抗原的起始功能,在体外阻断SV40 DNA的复制。

The murine p53 protein blocks replication of SV40 DNA in vitro by inhibiting the initiation functions of SV40 large T antigen.

作者信息

Wang E H, Friedman P N, Prives C

机构信息

Department of Biological Sciences, Columbia University, New York, New York 10027.

出版信息

Cell. 1989 May 5;57(3):379-92. doi: 10.1016/0092-8674(89)90913-6.

Abstract

We have characterized the effect of murine p53 on SV40 DNA replication in vitro. Purified wild-type murine p53 dramatically inhibited the ability of SV40 T antigen to mediate the replication of a plasmid bearing the viral origin (ori-DNA) in vitro. In contrast, polyoma ori-DNA replication in vitro was unaffected by p53. Surprisingly, both unbound p53 and SV40 T antigen-bound p53 were equally detrimental to SV40 ori-DNA replication. Thus, p53 interferes with interactions between T antigen molecules that are required for DNA synthesis. p53 inhibited the binding to and subsequent unwinding of the SV40 origin by T antigen and thus selectively blocked the initial stages of ori-DNA replication. In contrast to the nononcogenic wild-type murine p53, high concentrations of a mutant transforming p53 failed to block SV40 ori-DNA replication in vitro. These observations may provide insight into a possible role for p53 in the cell.

摘要

我们已经在体外对小鼠p53对SV40 DNA复制的影响进行了表征。纯化的野生型小鼠p53在体外显著抑制了SV40 T抗原介导携带病毒起源(ori-DNA)的质粒复制的能力。相比之下,多瘤病毒ori-DNA在体外的复制不受p53的影响。令人惊讶的是,未结合的p53和与SV40 T抗原结合的p53对SV40 ori-DNA复制同样有害。因此,p53干扰了DNA合成所需的T抗原分子之间的相互作用。p53抑制了T抗原与SV40起源的结合以及随后的解旋,从而选择性地阻断了ori-DNA复制的初始阶段。与非致癌性野生型小鼠p53不同,高浓度的突变型转化p53在体外未能阻断SV40 ori-DNA复制。这些观察结果可能有助于深入了解p53在细胞中的可能作用。

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