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水泡性口炎病毒缺陷干扰颗粒RNA全长互补物的体外合成。

Synthesis in vitro of the full-length complement of defective-interfering particle RNA of vesicular stomatitis virus.

作者信息

Chanda P K, Kang C Y, Banerjee A K

出版信息

Proc Natl Acad Sci U S A. 1980 Jul;77(7):3927-31. doi: 10.1073/pnas.77.7.3927.

DOI:10.1073/pnas.77.7.3927
PMID:6254002
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC349740/
Abstract

Under appropriate reaction conditions in vitro, four different defective-interfering particles of vesicular stomatitis virus have been shown to synthesize the full-length complement of their RNAs. The reaction involved preinitiation of the core particles with ATP and CTP, followed by RNA chain elongation in the presence of the beta, gamma-imido analogue of ATP, AdoPP[NH]P, and the three normal ribonucleoside triphosphates. By hybridization of the in vitro synthesized plus strand with the standard genome RNA followed by RNase treatment of the heteroduplexes, we have shown that the RNA of a defective-interfering particle derived from the 3' end of the genome RNA has evolved by an internal deletion of the standard genome.

摘要

在体外适当的反应条件下,已证明水疱性口炎病毒的四种不同缺陷干扰颗粒能够合成其RNA的全长互补序列。该反应包括用ATP和CTP对核心颗粒进行预起始,随后在ATP的β,γ-亚氨基类似物AdoPP[NH]P以及三种正常核糖核苷三磷酸存在的情况下进行RNA链延伸。通过将体外合成的正链与标准基因组RNA杂交,然后对异源双链体进行核糖核酸酶处理,我们已经表明,源自基因组RNA 3'端的缺陷干扰颗粒的RNA是通过标准基因组的内部缺失而进化的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d10/349740/3dc9d3d97217/pnas00494-0221-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d10/349740/76b13fbce0ce/pnas00494-0219-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d10/349740/3dc9d3d97217/pnas00494-0221-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d10/349740/76b13fbce0ce/pnas00494-0219-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d10/349740/3dc9d3d97217/pnas00494-0221-a.jpg

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Synthesis in vitro of the full-length complement of defective-interfering particle RNA of vesicular stomatitis virus.水泡性口炎病毒缺陷干扰颗粒RNA全长互补物的体外合成。
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引用本文的文献

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J Virol. 1981 Oct;40(1):78-86. doi: 10.1128/JVI.40.1.78-86.1981.
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Conditional synthesis of an aberrant glycoprotein mRNA by the internal deletion mutant of vesicular stomatitis virus.

本文引用的文献

1
Defective interfering particle generated by internal deletion of the vesicular stomatitis virus genome.由水疱性口炎病毒基因组内部缺失产生的缺陷干扰颗粒。
J Virol. 1980 Feb;33(2):818-29. doi: 10.1128/JVI.33.2.818-829.1980.
2
In vitro synthesis of the full-length complement of the negative-strand genome RNA of vesicular stomatitis virus.水疱性口炎病毒负链基因组RNA全长互补序列的体外合成
Proc Natl Acad Sci U S A. 1980 Jan;77(1):294-8. doi: 10.1073/pnas.77.1.294.
3
Persistent noncytocidal vesicular stomatitis virus infections mediated by defective T particles that suppress virion transcriptase.
水泡性口炎病毒内部缺失突变体对异常糖蛋白mRNA的条件性合成。
J Virol. 1983 Jun;46(3):709-17. doi: 10.1128/JVI.46.3.709-717.1983.
4
Transcription and replication of rhabdoviruses.弹状病毒的转录与复制
Microbiol Rev. 1987 Mar;51(1):66-87. doi: 10.1128/mr.51.1.66-87.1987.
由抑制病毒粒子转录酶的缺陷型T颗粒介导的持续性非杀细胞性水疱性口炎病毒感染。
Proc Natl Acad Sci U S A. 1974 Aug;71(8):2956-60. doi: 10.1073/pnas.71.8.2956.
4
Analysis of the RNA of defective VSV particles.缺陷型水泡性口炎病毒颗粒的RNA分析。
Cell. 1974 Sep;3(1):85-93. doi: 10.1016/0092-8674(74)90044-0.
5
The RNA of defective vesicular stomatitis virus particles in relation to viral cistrons.与病毒顺反子相关的缺陷性水疱性口炎病毒颗粒的RNA
J Mol Biol. 1974 Jan 5;85(4):551-68. doi: 10.1016/0022-2836(74)90315-5.
6
RNA polymerase activity and poly(A) synthesizing activity in defective T particles of vesicular stomatitis virus.水疱性口炎病毒缺陷型T颗粒中的RNA聚合酶活性和聚腺苷酸合成活性。
Virology. 1974 Mar;58(1):240-9. doi: 10.1016/0042-6822(74)90158-5.
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In vitro synthesis of RNA that contains polyadenylate by virion-associated RNA polymerase of vesicular stomatitis virus.水泡性口炎病毒的病毒粒子相关RNA聚合酶在体外合成含聚腺苷酸的RNA。
Proc Natl Acad Sci U S A. 1973 Dec;70(12):3566-70. doi: 10.1073/pnas.70.12.3566.
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Vesicular stomatitis virus--a new interfering particle, intracellular structures, and virus-specific RNA.水泡性口炎病毒——一种新的干扰颗粒、细胞内结构和病毒特异性RNA。
Virology. 1970 Aug;41(4):615-30. doi: 10.1016/0042-6822(70)90427-7.
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Proc Natl Acad Sci U S A. 1979 Dec;76(12):6191-5. doi: 10.1073/pnas.76.12.6191.