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含有沉默内部引导RNA基因的水疱性口炎病毒缺陷干扰颗粒。

Vesicular stomatitis virus defective interfering particle containing a muted internal leader RNA gene.

作者信息

Keene J D, Chien I M, Lazzarini R A

出版信息

Proc Natl Acad Sci U S A. 1981 Apr;78(4):2090-4. doi: 10.1073/pnas.78.4.2090.

DOI:10.1073/pnas.78.4.2090
PMID:6264463
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC319289/
Abstract

The RNA of a unique long defective interfering particle (DI-LT2) derived from the heat-resistant strain of vesicular stomatitis virus (VSV) contains 70 nucleotides at its 3' end that are complementary to the 5' end of the VSV RNA. Following this region of terminal complementarity, there is a precise copy of the 3' end of the nondefective VSV RNA. The sequence homology between the DI-LT2 RNA and the 3' end of VSV RNA extends for at least 60 bases and probably for most of the length of the DI-LT2 RNA. The DI-LT2 particle is capable of transcription in vitro but produces only a short RNA [defective interfering (DI) particle product], which is encoded by the extreme 3' terminus of the DI RNA. Neither leader RNA nor capped VSV mRNAs are synthesized by DI-LT2, although competent templates for these are present. These data suggest that the 3'-terminal initiation is a prerequisite of the production of competent transcripts and that the sequence coding for leader RNA is not, by itself, sufficient for initiation. We propose a model for the origin of this DI particle, involving specific termination and resumption of replication, which is similar to that described previously for another class of DI particle RNAs.

摘要

源自水疱性口炎病毒(VSV)耐热株的一种独特的长缺陷干扰颗粒(DI-LT2)的RNA,其3'端含有70个核苷酸,与VSV RNA的5'端互补。在这个末端互补区域之后,是无缺陷VSV RNA 3'端的精确拷贝。DI-LT2 RNA与VSV RNA 3'端之间的序列同源性至少延伸60个碱基,可能延伸至DI-LT2 RNA的大部分长度。DI-LT2颗粒能够在体外转录,但只产生一种短RNA [缺陷干扰(DI)颗粒产物],它由DI RNA的最末端3'端编码。DI-LT2既不合成前导RNA,也不合成加帽的VSV mRNA,尽管存在这些的有效模板。这些数据表明,3'端起始是产生有效转录本的先决条件,并且编码前导RNA的序列本身不足以起始。我们提出了一个关于这种DI颗粒起源的模型,涉及特定的复制终止和重新起始,这与之前描述的另一类DI颗粒RNA的情况类似。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6355/319289/63210959445c/pnas00655-0136-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6355/319289/8b0339fb4940/pnas00655-0134-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6355/319289/3abcf8d628fc/pnas00655-0135-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6355/319289/63210959445c/pnas00655-0136-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6355/319289/8b0339fb4940/pnas00655-0134-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6355/319289/3abcf8d628fc/pnas00655-0135-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6355/319289/63210959445c/pnas00655-0136-a.jpg

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Proc Natl Acad Sci U S A. 1981 Apr;78(4):2090-4. doi: 10.1073/pnas.78.4.2090.
2
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5
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Nucleotide sequence homology at the 3' termini of RNA from vesicular stomatitis virus and its defective interfering particles.水疱性口炎病毒及其缺陷干扰颗粒RNA 3'末端的核苷酸序列同源性。
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本文引用的文献

1
Polycistronic vesicular stomatitis virus RNA transcripts.多顺反子水泡性口炎病毒RNA转录本。
Proc Natl Acad Sci U S A. 1980 Aug;77(8):4662-5. doi: 10.1073/pnas.77.8.4662.
2
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.
3
Oligonucleotide sequence analyses indicate that vesicular stomatitis virus large defective interfering virus particle RNA is made by internal deletion: evidence for similar transcription polyadenylation signals for the synthesis of all vesicular stomatitis virus mRNA species.
由于启动子选择性增加导致仙台病毒基因组复制受到抑制:辅助C蛋白的潜在作用。
J Virol. 1997 Dec;71(12):9588-99. doi: 10.1128/JVI.71.12.9588-9599.1997.
4
Mutations within noncoding terminal sequences of model RNAs of Sendai virus: influence on reporter gene expression.仙台病毒模型RNA非编码末端序列内的突变:对报告基因表达的影响。
J Virol. 1995 Aug;69(8):5128-31. doi: 10.1128/JVI.69.8.5128-5131.1995.
5
Complete sequence analyses show that two defective interfering influenza viral RNAs contain a single internal deletion of a polymerase gene.完整的序列分析表明,两种缺陷干扰性流感病毒RNA包含一个聚合酶基因的单一内部缺失。
Proc Natl Acad Sci U S A. 1982 Apr;79(7):2216-20. doi: 10.1073/pnas.79.7.2216.
6
A host protein (La) binds to a unique species of minus-sense leader RNA during replication of vesicular stomatitis virus.在水疱性口炎病毒复制过程中,一种宿主蛋白(La)与一种独特的负义前导RNA结合。
Proc Natl Acad Sci U S A. 1983 Oct;80(19):5827-31. doi: 10.1073/pnas.80.19.5827.
7
Analysis of the recombination event generating a vesicular stomatitis virus deletion defective interfering particle.产生水疱性口炎病毒缺失型缺陷干扰颗粒的重组事件分析。
J Virol. 1983 Feb;45(2):766-72. doi: 10.1128/JVI.45.2.766-772.1983.
8
Genomic and copy-back 3' termini in Sendai virus defective interfering RNA species.仙台病毒缺陷干扰RNA物种中的基因组和回拷3'末端。
J Virol. 1983 Feb;45(2):659-64. doi: 10.1128/JVI.45.2.659-664.1983.
9
Sequence signal involved in the generation of an internally deleted defective interfering RNA from vesicular stomatitis virus.参与从水疱性口炎病毒产生内部缺失的缺陷干扰RNA的序列信号。
Nucleic Acids Res. 1982 Nov 11;10(21):6919-30. doi: 10.1093/nar/10.21.6919.
10
RNA polymerase-associated interactions near template promoter sequences of defective interfering particles of vesicular stomatitis virus.水疱性口炎病毒缺陷干扰颗粒模板启动子序列附近的RNA聚合酶相关相互作用。
J Virol. 1982 Jul;43(1):241-9. doi: 10.1128/JVI.43.1.241-249.1982.
寡核苷酸序列分析表明,水泡性口炎病毒大型缺陷干扰病毒颗粒RNA是通过内部缺失产生的:合成所有水泡性口炎病毒mRNA种类的转录多聚腺苷酸化信号相似的证据。
J Virol. 1980 Feb;33(2):807-17. doi: 10.1128/JVI.33.2.807-817.1980.
4
Intervening sequence between the leader region and the nucleopcapsid gene of vesicular stomatitis virus RNA.水疱性口炎病毒RNA的前导区与核衣壳基因之间的间隔序列。
J Virol. 1980 Feb;33(2):789-94. doi: 10.1128/JVI.33.2.789-794.1980.
5
Site on the vesicular stomatitis virus genome specifying polyadenylation and the end of the L gene mRNA.水疱性口炎病毒基因组上指定多聚腺苷酸化及L基因mRNA末端的位点。
J Virol. 1980 May;34(2):550-9. doi: 10.1128/JVI.34.2.550-559.1980.
6
Complete intergenic and flanking gene sequences from the genome of vesicular stomatitis virus.水疱性口炎病毒基因组的完整基因间隔区及侧翼基因序列。
Cell. 1980 Feb;19(2):415-21. doi: 10.1016/0092-8674(80)90515-2.
7
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.
8
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.
9
Degradation of DNA RNA hybrids by ribonuclease H and DNA polymerases of cellular and viral origin.细胞和病毒来源的核糖核酸酶H及DNA聚合酶对DNA-RNA杂交体的降解作用
Proc Natl Acad Sci U S A. 1972 Nov;69(11):3360-4. doi: 10.1073/pnas.69.11.3360.
10
Homotypic and heterotypic interference by defective particles of vesicular stomatitis virus.水泡性口炎病毒缺陷颗粒的同型和异型干扰
Nature. 1970 Oct 3;228(5266):25-7. doi: 10.1038/228025a0.