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从感染性互补DNA表达脊髓灰质炎病毒基因组取决于重组质粒中真核和原核序列的排列。

Expression of the poliovirus genome from infectious cDNA is dependent upon arrangements of eukaryotic and prokaryotic sequences in recombinant plasmids.

作者信息

Kuhn R J, Wimmer E, Semler B L

出版信息

Virology. 1987 Apr;157(2):560-4. doi: 10.1016/0042-6822(87)90302-3.

DOI:10.1016/0042-6822(87)90302-3
PMID:3029989
Abstract

The introduction of a cDNA copy of poliovirus type 1 (Mahoney) into cultured primate cells results in the production of infectious virus. The level of infectious virus can be increased by incorporation of eukaryotic signals of transcription and replication. We have utilized the SV40 DNA sequence coding for the early and late promoters, the SV40 origin of replication, and the enhancer elements, along with the cDNA of poliovirus, to determine the important parameters for the level of infectious virus produced following transfection. Although plasmid replication increases the level of infectivity, the major determinant of infectivity is promoter activity.

摘要

将脊髓灰质炎病毒1型(Mahoney株)的互补DNA(cDNA)拷贝导入培养的灵长类细胞中会产生传染性病毒。通过掺入真核转录和复制信号可提高传染性病毒的水平。我们利用编码早期和晚期启动子的猴病毒40(SV40)DNA序列、SV40复制起点和增强子元件,以及脊髓灰质炎病毒的cDNA,来确定转染后产生的传染性病毒水平的重要参数。虽然质粒复制会提高感染性水平,但感染性的主要决定因素是启动子活性。

相似文献

1
Expression of the poliovirus genome from infectious cDNA is dependent upon arrangements of eukaryotic and prokaryotic sequences in recombinant plasmids.从感染性互补DNA表达脊髓灰质炎病毒基因组取决于重组质粒中真核和原核序列的排列。
Virology. 1987 Apr;157(2):560-4. doi: 10.1016/0042-6822(87)90302-3.
2
Production of infectious poliovirus from cloned cDNA is dramatically increased by SV40 transcription and replication signals.通过SV40转录和复制信号,从克隆的cDNA产生感染性脊髓灰质炎病毒的效率显著提高。
Nucleic Acids Res. 1984 Jun 25;12(12):5123-41. doi: 10.1093/nar/12.12.5123.
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Highly infectious plasmids carrying poliovirus cDNA are capable of replication in transfected simian cells.携带脊髓灰质炎病毒互补脱氧核糖核酸的高传染性质粒能够在转染的猿猴细胞中复制。
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A chimeric plasmid from cDNA clones of poliovirus and coxsackievirus produces a recombinant virus that is temperature-sensitive.一种来自脊髓灰质炎病毒和柯萨奇病毒cDNA克隆的嵌合质粒产生了一种温度敏感的重组病毒。
Proc Natl Acad Sci U S A. 1986 Mar;83(6):1777-81. doi: 10.1073/pnas.83.6.1777.
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Simian virus 40 late promoter region able to initiate simian virus 40 early gene transcription in the absence of the simian virus 40 origin sequence.猿猴病毒40晚期启动子区域,能够在没有猿猴病毒40起源序列的情况下启动猿猴病毒40早期基因转录。
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Long-range activation of transcription by SV40 enhancer is affected by "inhibitory" or "permissive" DNA sequences between enhancer and promoter.SV40增强子对转录的远程激活受到增强子与启动子之间“抑制性”或“许可性”DNA序列的影响。
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Repression of simian virus 40 early transcription by viral DNA replication in human 293 cells.
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Transcriptional 'enhancers' from SV40 and polyoma virus show a cell type preference.来自猴病毒40(SV40)和多瘤病毒的转录“增强子”表现出细胞类型偏好性。
Nucleic Acids Res. 1982 Dec 20;10(24):7965-76. doi: 10.1093/nar/10.24.7965.
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Sequences involved in initiation of simian virus 40 late transcription in the absence of T antigen.在缺乏T抗原的情况下,参与猿猴病毒40晚期转录起始的序列。
Mol Cell Biol. 1986 Jun;6(6):1875-85. doi: 10.1128/mcb.6.6.1875-1885.1986.

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Nucleic Acids Res. 1993 Jun 11;21(11):2703-8. doi: 10.1093/nar/21.11.2703.
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