• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

猿猴病毒40复制起点的区域界限和功能解剖结构。

Territorial limits and functional anatomy of the simian virus 40 replication origin.

作者信息

Bergsma D J, Olive D M, Hartzell S W, Subramanian K N

出版信息

Proc Natl Acad Sci U S A. 1982 Jan;79(2):381-5. doi: 10.1073/pnas.79.2.381.

DOI:10.1073/pnas.79.2.381
PMID:6281769
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC345744/
Abstract

The region at and near the simian virus 40 (SV40) DNA replication origin contains a series of palindromes, a 17-base pair (bp) A + T-rich sequence, three copies of a 21-bp repeat, and two copies of a 72-bp repeat. We have constructed a series of recombinant plasmids containing sequential deletions at the region of SV40 DNA replication origin starting from the end near the repeats. These deletions were introduced by using in vitro and in vivo techniques. The relative replication efficiency of these recombinant plasmids were directly assayed in COS-1 monkey kidney cells capable of providing the tumor antigen necessary for the replication of these molecules. Recombinants lacking both copies of the 72-bp repeat did not exhibit any reduction in replication efficiency. Recombinants lacking the 21-bp repeats showed decreased replication efficiency; the reduction in replication efficiency was proportional to the number of copies of the 21-bp repeat deleted in these recombinants. A recombinant retaining the palindromes at the region of SV40 DNA replication but lacking the A + T-rich sequence and the repeats failed to replicate. Based on these results, the SV40 DNA replication origin is subdivided into two regions, and their boundaries are defined. One of these two regions is a core region containing the 17-bp, 15-bp, and 27-bp palindromes and, quite likely, the 17-bp A + T-rich sequence which are necessary for replication. The other is an auxiliary region that consists of the 21-bp repeats and has a dose-dependent enhancement effect on replication efficiency.

摘要

猿猴病毒40(SV40)DNA复制起点及其附近区域包含一系列回文序列、一个17碱基对(bp)的富含A+T的序列、三个21 bp重复序列拷贝以及两个72 bp重复序列拷贝。我们构建了一系列重组质粒,这些质粒在SV40 DNA复制起点区域从靠近重复序列的一端开始进行连续缺失。这些缺失通过体外和体内技术引入。这些重组质粒的相对复制效率在能够提供这些分子复制所需肿瘤抗原的COS-1猴肾细胞中直接进行测定。缺乏两个72 bp重复序列拷贝的重组体在复制效率上没有表现出任何降低。缺乏21 bp重复序列的重组体显示复制效率降低;复制效率的降低与这些重组体中缺失的21 bp重复序列拷贝数成比例。一个在SV40 DNA复制区域保留回文序列但缺乏富含A+T的序列和重复序列的重组体无法复制。基于这些结果,SV40 DNA复制起点被细分为两个区域,并确定了它们的边界。这两个区域中的一个是核心区域,包含17 bp、15 bp和27 bp的回文序列,很可能还包含复制所必需的17 bp富含A+T的序列。另一个是辅助区域,由21 bp重复序列组成,对复制效率具有剂量依赖性增强作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9fd/345744/2291399bf19a/pnas00441-0184-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9fd/345744/7b8c83312bf8/pnas00441-0184-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9fd/345744/2291399bf19a/pnas00441-0184-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9fd/345744/7b8c83312bf8/pnas00441-0184-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9fd/345744/2291399bf19a/pnas00441-0184-b.jpg

相似文献

1
Territorial limits and functional anatomy of the simian virus 40 replication origin.猿猴病毒40复制起点的区域界限和功能解剖结构。
Proc Natl Acad Sci U S A. 1982 Jan;79(2):381-5. doi: 10.1073/pnas.79.2.381.
2
Replication from a proximal simian virus 40 origin is severely inhibited by multiple reiterations of the 72-base-pair repeat enhancer sequence.来自近端猿猴病毒40起始位点的复制受到72个碱基对重复增强子序列多次重复的严重抑制。
Mol Cell Biol. 1988 Apr;8(4):1509-17. doi: 10.1128/mcb.8.4.1509-1517.1988.
3
Definition of the simian virus 40 early promoter region and demonstration of a host range bias in the enhancement effect of the simian virus 40 72-base-pair repeat.猿猴病毒40早期启动子区域的定义以及猿猴病毒40 72碱基对重复序列增强效应中宿主范围偏向性的证明。
Proc Natl Acad Sci U S A. 1983 Feb;80(3):721-5. doi: 10.1073/pnas.80.3.721.
4
Effects of position and orientation of the 72-base-pair-repeat transcriptional enhancer on replication from the simian virus 40 core origin.72碱基对重复转录增强子的位置和方向对猿猴病毒40核心起点复制的影响。
J Virol. 1987 Oct;61(10):2973-80. doi: 10.1128/JVI.61.10.2973-2980.1987.
5
Sequence requirements for activation of replication by the SV40 transcriptional promoter or enhancer elements.SV40转录启动子或增强子元件激活复制的序列要求。
Virology. 1991 Jan;180(1):41-8. doi: 10.1016/0042-6822(91)90007-x.
6
Extension of JC virus host range to monkey cells by insertion of a simian virus 40 enhancer into the JC virus regulatory region.通过将猿猴病毒40增强子插入JC病毒调控区域,使JC病毒宿主范围扩展至猴细胞。
Virology. 1989 Jun;170(2):353-61. doi: 10.1016/0042-6822(89)90425-x.
7
Relationship among location of T-antigen-induced DNA distortion, auxiliary sequences, and DNA replication efficiency.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。
J Virol. 2003 Oct;77(19):10651-7. doi: 10.1128/jvi.77.19.10651-10657.2003.
8
Simian virus 40 DNA replication: functional organization of regulatory elements.猿猴病毒40 DNA复制:调控元件的功能组织
Mol Cell Biol. 1986 Sep;6(9):3086-93. doi: 10.1128/mcb.6.9.3086-3093.1986.
9
The SV40 72 base repair repeat has a striking effect on gene expression both in SV40 and other chimeric recombinants.SV40的72碱基修复重复序列对SV40及其他嵌合重组体中的基因表达均有显著影响。
Nucleic Acids Res. 1981 Nov 25;9(22):6047-68. doi: 10.1093/nar/9.22.6047.
10
The simian virus 40 minimal origin and the 72-base-pair repeat are required simultaneously for efficient induction of late gene expression with large tumor antigen.猿猴病毒40最小起始区和72碱基对重复序列同时存在时,才能通过大肿瘤抗原有效诱导晚期基因表达。
Proc Natl Acad Sci U S A. 1984 Oct;81(20):6335-9. doi: 10.1073/pnas.81.20.6335.

引用本文的文献

1
The evolutionary loss of the Eh1 motif in FoxE1 in the lineage of placental mammals.FoxE1 中 Eh1 基序在胎盘哺乳动物谱系中的进化丢失。
PLoS One. 2023 Dec 27;18(12):e0296176. doi: 10.1371/journal.pone.0296176. eCollection 2023.
2
Regulation of Human Papillomavirus 18 Genome Replication, Establishment, and Persistence by Sequences in the Viral Upstream Regulatory Region.调控人乳头瘤病毒 18 基因组复制、建立和持续性的病毒上游调控区序列。
J Virol. 2021 Sep 9;95(19):e0068621. doi: 10.1128/JVI.00686-21.
3
Development of quantitative and high-throughput assays of polyomavirus and papillomavirus DNA replication.

本文引用的文献

1
Simian virus 40 tandem repeated sequences as an element of the early promoter.猿猴病毒40串联重复序列作为早期启动子的一个元件
Proc Natl Acad Sci U S A. 1981 Feb;78(2):943-7. doi: 10.1073/pnas.78.2.943.
2
SV40-transformed simian cells support the replication of early SV40 mutants.猴空泡病毒 40(SV40)转化的猿猴细胞支持早期 SV40 突变体的复制。
Cell. 1981 Jan;23(1):175-82. doi: 10.1016/0092-8674(81)90282-8.
3
In vivo sequence requirements of the SV40 early promotor region.猴空泡病毒40早期启动子区域的体内序列要求
开发用于检测多瘤病毒和乳头瘤病毒 DNA 复制的定量和高通量检测方法。
Virology. 2010 Mar 30;399(1):65-76. doi: 10.1016/j.virol.2009.12.026. Epub 2010 Jan 15.
4
Complete Sequence and Enhancer Function of the Homologous DNA Regions of Autographa californica Nuclear Polyhedrosis Virus.苜蓿银纹夜蛾核型多角体病毒同源DNA区域的完整序列及增强子功能
J Virol. 1986 Oct;60(1):224-9. doi: 10.1128/JVI.60.1.224-229.1986.
5
Interspersed Homologous DNA of Autographa californica Nuclear Polyhedrosis Virus Enhances Delayed-Early Gene Expression.苜蓿银纹夜蛾核型多角体病毒的散布同源DNA增强延迟早期基因表达。
J Virol. 1986 Oct;60(1):215-23. doi: 10.1128/JVI.60.1.215-223.1986.
6
In search of the holy replicator.寻找神圣的复制器。
Nat Rev Mol Cell Biol. 2004 Oct;5(10):848-55. doi: 10.1038/nrm1495.
7
Relationship among location of T-antigen-induced DNA distortion, auxiliary sequences, and DNA replication efficiency.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。
J Virol. 2003 Oct;77(19):10651-7. doi: 10.1128/jvi.77.19.10651-10657.2003.
8
Transcription from the SV40 early-early and late-early overlapping promoters in the absence of DNA replication.在不存在DNA复制的情况下,从SV40早期早期和晚期早期重叠启动子进行转录。
EMBO J. 1983;2(9):1605-11. doi: 10.1002/j.1460-2075.1983.tb01631.x.
9
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。
J Virol. 2001 Jun;75(12):5638-45. doi: 10.1128/JVI.75.12.5638-5645.2001.
10
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
J Virol. 1999 Dec;73(12):10254-63. doi: 10.1128/JVI.73.12.10254-10263.1999.
Nature. 1981 Mar 26;290(5804):304-10. doi: 10.1038/290304a0.
4
Construction and analysis of simian virus 40 origins defective in tumor antigen binding and DNA replication.在肿瘤抗原结合和DNA复制方面存在缺陷的猿猴病毒40起源的构建与分析。
Proc Natl Acad Sci U S A. 1980 Nov;77(11):6491-5. doi: 10.1073/pnas.77.11.6491.
5
Integration in vivo into simian virus 40 DNA of a sequence that resembles a certain family of genomic interspersed repeated sequences.在体内整合到猿猴病毒40 DNA中一段类似于某一基因组散布重复序列家族的序列。
Proc Natl Acad Sci U S A. 1980 Aug;77(8):4514-8. doi: 10.1073/pnas.77.8.4514.
6
Expression of early genes of origin-defective mutants of simian virus 40.猴病毒40起源缺陷型突变体早期基因的表达
Proc Natl Acad Sci U S A. 1980 Jul;77(7):3898-902. doi: 10.1073/pnas.77.7.3898.
7
Isolation of mutants of an animal virus in bacteria.在细菌中分离动物病毒的突变体。
Science. 1980 Sep 19;209(4463):1392-6. doi: 10.1126/science.6251547.
8
Cold-sensitive regulatory mutants of simian virus 40.猿猴病毒40的冷敏感调节突变体
J Mol Biol. 1980 Jun 15;140(1):129-42. doi: 10.1016/0022-2836(80)90359-9.
9
Mapping of SV40 DNA replication origin region binding sites for the SV40 T antigen by protection against exonuclease III digestion.通过抗核酸外切酶III消化法对SV40 T抗原的SV40 DNA复制起始区域结合位点进行定位。
Cell. 1980 Jun;20(2):411-22. doi: 10.1016/0092-8674(80)90627-3.
10
Sequencing end-labeled DNA with base-specific chemical cleavages.通过碱基特异性化学切割对末端标记的DNA进行测序。
Methods Enzymol. 1980;65(1):499-560. doi: 10.1016/s0076-6879(80)65059-9.