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1
Transcription of vesicular stomatitis virus is required to shut off cellular RNA synthesis.水泡性口炎病毒的转录对于关闭细胞RNA合成是必需的。
J Virol. 1979 Apr;30(1):410-3. doi: 10.1128/JVI.30.1.410-413.1979.
2
Use of UV irradiation to identify the genetic information of vesicular stomatitis virus responsible for shutting off cellular RNA synthesis.利用紫外线照射鉴定水泡性口炎病毒中负责阻断细胞RNA合成的遗传信息。
J Virol. 1979 Jun;30(3):746-53. doi: 10.1128/JVI.30.3.746-753.1979.
3
Inhibition of RNA synthesis in mouse myeloma cells infected with vesicular stomatitis virus.水泡性口炎病毒感染的小鼠骨髓瘤细胞中RNA合成的抑制作用
J Virol. 1978 Mar;25(3):770-80. doi: 10.1128/JVI.25.3.770-780.1978.
4
Differential inhibition of host protein synthesis in L cells infected with RNA - temperature-sensitive mutants of vesicular stomatitis virus.水泡性口炎病毒RNA温度敏感突变体感染的L细胞中宿主蛋白合成的差异抑制
J Virol. 1976 May;18(2):550-8. doi: 10.1128/JVI.18.2.550-558.1976.
5
RNA synthesis in temperature-sensitive mutants of vesicular stomatitis virus.水泡性口炎病毒温度敏感突变体中的RNA合成
J Virol. 1973 Sep;12(3):570-8. doi: 10.1128/JVI.12.3.570-578.1973.
6
Location of the transcription defect in group I temperature-sensitive mutants of vesicular stomatitis virus.水泡性口炎病毒I组温度敏感突变体中转录缺陷的定位
J Virol. 1974 Jan;13(1):28-35. doi: 10.1128/JVI.13.1.28-35.1974.
7
Further studies of the RNA synthesis phenotype selected during persistent infection with vesicular stomatitis virus.对水泡性口炎病毒持续感染期间选择的RNA合成表型的进一步研究。
Virology. 1984 Jul 15;136(1):211-20. doi: 10.1016/0042-6822(84)90260-5.
8
Temperature-sensitive mutants of vesicular stomatitis virus: synthesis of virus-specific proteins.水泡性口炎病毒的温度敏感突变体:病毒特异性蛋白质的合成
J Virol. 1971 May;7(5):651-62. doi: 10.1128/JVI.7.5.651-662.1971.
9
Inhibition of cellular DNA synthesis by vesicular stomatitis virus.水泡性口炎病毒对细胞DNA合成的抑制作用。
J Virol. 1981 Apr;38(1):356-67. doi: 10.1128/JVI.38.1.356-367.1981.
10
Inhibition of ribonucleic acid accumulation in mouse L cells infected with vesicular stomatitis virus requires viral ribonucleic acid transcription.抑制感染水疱性口炎病毒的小鼠L细胞中核糖核酸的积累需要病毒核糖核酸转录。
Biochemistry. 1980 Feb 19;19(4):804-10. doi: 10.1021/bi00545a029.

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Dominant inhibition of Akt/protein kinase B signaling by the matrix protein of a negative-strand RNA virus.负链 RNA 病毒基质蛋白对 Akt/蛋白激酶 B 信号通路的显性抑制作用。
J Virol. 2011 Jan;85(1):422-31. doi: 10.1128/JVI.01671-10. Epub 2010 Oct 27.
2
Cytopathogenesis and inhibition of host gene expression by RNA viruses.RNA病毒的细胞发病机制及对宿主基因表达的抑制
Microbiol Mol Biol Rev. 2000 Dec;64(4):709-24. doi: 10.1128/MMBR.64.4.709-724.2000.
3
Effect of vesicular stomatitis virus matrix protein on transcription directed by host RNA polymerases I, II, and III.水泡性口炎病毒基质蛋白对宿主RNA聚合酶I、II和III指导的转录的影响。
J Virol. 1998 Oct;72(10):8413-9. doi: 10.1128/JVI.72.10.8413-8419.1998.
4
Migration of vesicular stomatitis virus glycoprotein to the nucleus of infected cells.水泡性口炎病毒糖蛋白向受感染细胞细胞核的迁移。
Proc Natl Acad Sci U S A. 1996 Aug 6;93(16):8268-73. doi: 10.1073/pnas.93.16.8268.
5
Effect of vesicular stomatitis virus matrix protein on host-directed translation in vivo.水泡性口炎病毒基质蛋白对体内宿主导向翻译的影响。
J Virol. 1994 Jan;68(1):555-60. doi: 10.1128/JVI.68.1.555-560.1994.
6
Nucleotide sequence and host La protein interactions of rabies virus leader RNA.狂犬病病毒前导RNA的核苷酸序列及其与宿主La蛋白的相互作用
J Virol. 1984 Jun;50(3):773-8. doi: 10.1128/JVI.50.3.773-778.1984.
7
Comparative inhibition of cellular transcription by vesicular stomatitis virus serotypes New Jersey and Indiana: role of each viral leader RNA.水疱性口炎病毒新泽西型和印第安纳型对细胞转录的比较抑制作用:各病毒前导RNA的作用
J Virol. 1983 Oct;48(1):88-101. doi: 10.1128/JVI.48.1.88-101.1983.
8
Inhibition of cellular DNA synthesis by vesicular stomatitis virus.水泡性口炎病毒对细胞DNA合成的抑制作用。
J Virol. 1981 Apr;38(1):356-67. doi: 10.1128/JVI.38.1.356-367.1981.
9
Homotypic and heterotypic exclusion of vesicular stomatitis virus replication by high levels of recombinant polymerase protein L.高水平重组聚合酶蛋白L对水疱性口炎病毒复制的同型和异型排斥
J Virol. 1987 Oct;61(10):3133-42. doi: 10.1128/JVI.61.10.3133-3142.1987.
10
Rapid inhibition of processing and assembly of small nuclear ribonucleoproteins after infection with vesicular stomatitis virus.感染水疱性口炎病毒后小核核糖核蛋白的加工和组装迅速受到抑制。
Mol Cell Biol. 1987 Mar;7(3):1148-55. doi: 10.1128/mcb.7.3.1148-1155.1987.

本文引用的文献

1
Control mechanism of ribonucleic acid synthesis in eukaryotes. The effect of amino acid and glucose starvation and cycloheximide on yeast deoxyribonucleic acid-dependent ribonucleic acid polymerases.真核生物中核糖核酸合成的控制机制。氨基酸和葡萄糖饥饿以及环己酰亚胺对酵母脱氧核糖核酸依赖性核糖核酸聚合酶的影响。
J Biol Chem. 1974 Jan 25;249(2):568-76.
2
Transcription and replication of vesicular stomatitis virus: effects of temperature-sensitive mutations in complementation group IV.水泡性口炎病毒的转录与复制:互补群IV中温度敏感突变的影响
J Virol. 1974 Apr;13(4):922-30. doi: 10.1128/JVI.13.4.922-930.1974.
3
Cell killing by viruses. I. Comparison of cell-killing, plaque-forming, and defective-interfering particles of vesicular stomatitis virus.病毒导致的细胞杀伤。I. 水疱性口炎病毒的细胞杀伤、噬斑形成及缺陷干扰颗粒的比较
Virology. 1974 Feb;57(2):321-38. doi: 10.1016/0042-6822(74)90172-x.
4
Location of the transcription defect in group I temperature-sensitive mutants of vesicular stomatitis virus.水泡性口炎病毒I组温度敏感突变体中转录缺陷的定位
J Virol. 1974 Jan;13(1):28-35. doi: 10.1128/JVI.13.1.28-35.1974.
5
Primary in vivo transcription of vesicular stomatitis virus and temperature-sensitive mutants of five vesicular stomatitis virus complementation groups.水泡性口炎病毒及其五个互补组的温度敏感突变体的体内初级转录
J Virol. 1973 Dec;12(6):1238-52. doi: 10.1128/JVI.12.6.1238-1252.1973.
6
[Thermosensitive mutants of vesicular stomatitis virus of complementation group II (author's transl)].水泡性口炎病毒互补群II的热敏突变体(作者译)
Ann Microbiol (Paris). 1973 Mar;124(2):261-9.
7
RNA synthesis in temperature-sensitive mutants of vesicular stomatitis virus.水泡性口炎病毒温度敏感突变体中的RNA合成
J Virol. 1973 Sep;12(3):570-8. doi: 10.1128/JVI.12.3.570-578.1973.
8
Effect of temperature-sensitive mutations on the virion-associated RNA transcriptase of vesicular stomatitis virus.温度敏感突变对水疱性口炎病毒病毒体相关RNA转录酶的影响。
J Mol Biol. 1972 Nov 14;71(2):281-91. doi: 10.1016/0022-2836(72)90351-8.
9
Inhibition of protein synthesis in L cells infected with vesicular stomatitis virus.水泡性口炎病毒感染的L细胞中蛋白质合成的抑制作用
J Virol. 1972 Jan;9(1):85-9. doi: 10.1128/JVI.9.1.85-89.1972.
10
[Genetic study of vesicular stomatitis virus: classification of spontaneous thermosensitive mutants into complementation groups].[水疱性口炎病毒的遗传学研究:将自发热敏突变体分类为互补群]
J Gen Virol. 1970 Sep;8(3):187-95. doi: 10.1099/0022-1317-8-3-187.

水泡性口炎病毒的转录对于关闭细胞RNA合成是必需的。

Transcription of vesicular stomatitis virus is required to shut off cellular RNA synthesis.

作者信息

Weck P K, Wagner R R

出版信息

J Virol. 1979 Apr;30(1):410-3. doi: 10.1128/JVI.30.1.410-413.1979.

DOI:10.1128/JVI.30.1.410-413.1979
PMID:225526
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC353338/
Abstract

RNA synthesis by mouse myeloma (MPC-11) cells was rapidly and progressively shut off by infection with vesicular stomatitis virus temperature-sensitive (ts) mutants permissive for transcription. In sharp contrast, mutants or defective vesicular stomatitis virions restricted in transcription were incapable of causing progressive inhibition of cellular RNA synthesis even at massive multiplicities of infection. A viral product synthesized 30 to 60 min after permissive infection with tsG114(I) appeared to be essential for prolonged inhibition of RNA synthesis in cells switched up to restrictive temperature.

摘要

感染允许转录的水泡性口炎病毒温度敏感(ts)突变体后,小鼠骨髓瘤(MPC - 11)细胞的RNA合成迅速且逐渐被关闭。与之形成鲜明对比的是,转录受限的突变体或缺陷型水泡性口炎病毒粒子,即使在大量感染复数的情况下,也无法对细胞RNA合成造成渐进性抑制。在允许温度下感染tsG114(I) 30至60分钟后合成的一种病毒产物,似乎是在切换到限制温度的细胞中长时间抑制RNA合成所必需的。