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T抗原对猴病毒40复制起点结构变化的差异诱导

Differential induction of structural changes in the simian virus 40 origin of replication by T antigen.

作者信息

Borowiec J A, Dean F B, Hurwitz J

机构信息

Program in Molecular Biology and Virology, Memorial Sloan-Kettering Cancer Center, New York, New York 10021.

出版信息

J Virol. 1991 Mar;65(3):1228-35. doi: 10.1128/JVI.65.3.1228-1235.1991.

Abstract

The ATP-dependent binding of the simian virus 40 (SV40) large tumor antigen (T antigen) to the SV40 origin of replication (ori) results in the structural distortion of two critical elements within flanking regions of ori and the untwisting of the DNA helix. We examined the effect of changes in temperature, ATP concentration, and other reaction parameters on the generation of these DNA structural changes. We found that induction of the two localized structural transitions were highly and differentially sensitive to reaction conditions. Significant distortion of the early palindrome element, shown previously to result from DNA melting, required low levels of ATP (10 to 30 microM) but temperatures above 25 degrees C. Distortion of the AT tract occurred at low temperatures (5 degrees C) but required relatively high concentrations of ATP (greater than 300 microM). Thus, T antigen can induce structural changes within one critical element of ori without generating significant structural distortion within the second element. The response of ori untwisting to reaction conditions generally increased in parallel with or fell intermediate between the inductions of localized structural transitions. We suggest that ori untwisting and localized structural distortions are interdependent consequences of T-antigen binding to ori. These results suggest a model for the structural events occurring during the initial steps of SV40 DNA replication.

摘要

猿猴病毒40(SV40)大T抗原(T抗原)与SV40复制起点(ori)的ATP依赖性结合导致ori侧翼区域内两个关键元件的结构扭曲以及DNA螺旋的解旋。我们研究了温度、ATP浓度和其他反应参数的变化对这些DNA结构变化产生的影响。我们发现,这两种局部结构转变的诱导对反应条件高度敏感且存在差异。先前显示由DNA解链导致的早期回文元件的显著扭曲需要低水平的ATP(10至30微摩尔),但温度要高于25摄氏度。AT序列的扭曲发生在低温(5摄氏度)下,但需要相对较高浓度的ATP(大于300微摩尔)。因此,T抗原可以在ori的一个关键元件内诱导结构变化,而不会在第二个元件内产生显著的结构扭曲。ori解旋对反应条件的响应通常与局部结构转变的诱导平行增加或介于两者之间。我们认为ori解旋和局部结构扭曲是T抗原与ori结合的相互依存的结果。这些结果提出了一个关于SV40 DNA复制初始步骤中发生的结构事件的模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3807/239892/1d3199df8340/jvirol00046-0190-a.jpg

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