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本文引用的文献

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Epstein-Barr nuclear antigen 1 binds and destabilizes nucleosomes at the viral origin of latent DNA replication.爱泼斯坦-巴尔核抗原1在潜伏性DNA复制的病毒起源处结合并使核小体不稳定。
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Intrinsic DNA bends: an organizer of local chromatin structure for transcription.内在DNA弯曲:转录的局部染色质结构组织者。
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DNA replication efficiency depends on transcription factor-binding sites.DNA复制效率取决于转录因子结合位点。
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Review: nuclear structure and DNA replication.综述:核结构与DNA复制。
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Conformational changes in simian virus 40 rearranged regulatory regions: effects of the 21-base-pair promoters and their location.猴病毒40重排调控区的构象变化:21个碱基对启动子的作用及其位置
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The initiation of simian virus 40 DNA replication in vitro.猿猴病毒40 DNA在体外的复制起始
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TBP binding to the TATA box induces a specific downstream unwinding site that is targeted by pluramycin.TBP与TATA盒结合会诱导一个特定的下游解旋位点,该位点是嘌呤霉素的作用靶点。
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A model for the T-antigen-induced structural alteration of the SV40 replication origin based upon experiments with specific probes for bent, straight, and unwound DNA.基于针对弯曲、直线和解旋DNA的特异性探针实验得出的T抗原诱导SV40复制起点结构改变的模型。
Biochemistry. 1996 Jun 18;35(24):7993-8001. doi: 10.1021/bi960251d.
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Action at a distance: DNA-looping and initiation of transcription.远距离作用:DNA 环化与转录起始
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(+)-CC-1065 as a structural probe of Mu transposase-induced bending of DNA: overcoming limitations of hydroxyl-radical footprinting.
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T抗原诱导的DNA扭曲位置、辅助序列与DNA复制效率之间的关系。

Relationship among location of T-antigen-induced DNA distortion, auxiliary sequences, and DNA replication efficiency.

作者信息

Okuley Susan, Call Mindy, Mitchell Tara, Hu Bugen, Woodworth Mary E

机构信息

Department of Microbiology, Miami University, Oxford, Ohio 45056, USA.

出版信息

J Virol. 2003 Oct;77(19):10651-7. doi: 10.1128/jvi.77.19.10651-10657.2003.

DOI:10.1128/jvi.77.19.10651-10657.2003
PMID:12970450
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC228485/
Abstract

T-antigen-induced DNA distortion was studied in a series of simian virus 40 (SV40) plasmid constructs whose relative replication efficiency ranges from 0.2 to 36. Bending was detected in the wild-type SV40 regulatory region consisting of three copies of the GC-rich 21-bp repeat but not in constructs with only one or two copies of the 21-bp repeat. In a construct with enhanced replication efficiency, bending occurred in a 69-bp cellular sequence located upstream of a single copy of the 21-bp repeat. Bending occurred both upstream of ori and in the three 21-bp repeats located downstream of ori in a construct with reduced replication efficiency. In a construct with no 21-bp repeats, DNA distortion occurred downstream of ori. The results indicate that SV40 DNA replication is enhanced when the structure of the regulatory region allows the DNA to form a bent structure upstream of the initial movement of the replication fork.

摘要

在一系列猿猴病毒40(SV40)质粒构建体中研究了T抗原诱导的DNA扭曲,这些构建体的相对复制效率范围为0.2至36。在由富含GC的21碱基重复序列的三个拷贝组成的野生型SV40调控区域中检测到弯曲,但在仅具有一个或两个21碱基重复序列拷贝的构建体中未检测到弯曲。在一个复制效率增强的构建体中,弯曲发生在位于21碱基重复序列单拷贝上游的69碱基细胞序列中。在一个复制效率降低的构建体中,弯曲发生在ori上游以及位于ori下游的三个21碱基重复序列中。在一个没有21碱基重复序列的构建体中,DNA扭曲发生在ori下游。结果表明,当调控区域的结构允许DNA在复制叉初始移动上游形成弯曲结构时,SV40 DNA复制会增强。