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人拓扑异构酶1信使核糖核酸不会因2型单纯疱疹病毒的病毒体相关关闭功能而变得不稳定。

Human topoisomerase 1 messenger RNA is not destabilized by the herpes simplex virus type 2 virion-associated shut-off function.

作者信息

Bastow K F, Zhou B S, Cheng Y C

机构信息

Department of Pharmacology, School of Medicine, University of North Carolina, Chapel Hill 27599-7365.

出版信息

Virus Genes. 1989 Aug;2(4):357-65. doi: 10.1007/BF00684043.

DOI:10.1007/BF00684043
PMID:2554584
Abstract

A cDNA for human topoisomerase I (Topo 1) was used to identify a 4.1 kb polyadenylated Topo 1 mRNA in methotrexate-resistant human KB cells that are permissive for herpes simplex virus type 2 (HSV-2) infection. Using these cells, no effect of the HSV-2-associated early shut-off function on levels of Topo-1 mRNA was observed up to 6 hours postinfection, whereas the actin mRNA level was 22% cellular transcripts are susceptible. The level of several host-cell polyadenylated RNAs detected as cDNA clones (class 3 transcripts) were unchanged 8 hours after HSV-2 infection, and other cellular transcripts (class 2) actually accumulated at postinfection.

摘要

用人拓扑异构酶I(Topo 1)的互补DNA(cDNA),在对单纯疱疹病毒2型(HSV - 2)感染敏感的耐甲氨蝶呤人KB细胞中鉴定出一个4.1 kb的聚腺苷酸化Topo 1信使核糖核酸(mRNA)。利用这些细胞,在感染后长达6小时内,未观察到HSV - 2相关的早期关闭功能对Topo - 1 mRNA水平有影响,而肌动蛋白mRNA水平在感染后6小时是细胞转录本的22%。HSV - 2感染8小时后,作为cDNA克隆检测到的几种宿主细胞聚腺苷酸化RNA(3类转录本)水平未变,而其他细胞转录本(2类)在感染后实际有所积累。

相似文献

1
Human topoisomerase 1 messenger RNA is not destabilized by the herpes simplex virus type 2 virion-associated shut-off function.人拓扑异构酶1信使核糖核酸不会因2型单纯疱疹病毒的病毒体相关关闭功能而变得不稳定。
Virus Genes. 1989 Aug;2(4):357-65. doi: 10.1007/BF00684043.
2
Synthesis of dihydrofolate reductase and metabolism of related RNA in a methotrexate resistant human cell line infected with herpes simplex virus type 2.
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Studies on DNA topoisomerases I and II in herpes simplex virus type 2-infected cells.2型单纯疱疹病毒感染细胞中DNA拓扑异构酶I和II的研究。
J Gen Virol. 1987 Aug;68 ( Pt 8):2231-7. doi: 10.1099/0022-1317-68-8-2231.
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Effect of herpes simplex virus type-1 UL41 gene on the stability of mRNA from the cellular genes: beta-actin, fibronectin, glucose transporter-1, and docking protein, and on virus intraperitoneal pathogenicity to newborn mice.单纯疱疹病毒1型UL41基因对细胞基因β-肌动蛋白、纤连蛋白、葡萄糖转运蛋白1及对接蛋白的mRNA稳定性以及对新生小鼠病毒腹腔致病性的影响。
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Herpes simplex virus-infected cells contain a function(s) that destabilizes both host and viral mRNAs.单纯疱疹病毒感染的细胞含有一种或多种使宿主和病毒mRNA都不稳定的功能。
Proc Natl Acad Sci U S A. 1987 Apr;84(7):1926-30. doi: 10.1073/pnas.84.7.1926.
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Early and delayed shut-off of host protein synthesis in cells infected with herpes simplex virus.单纯疱疹病毒感染细胞中宿主蛋白质合成的早期和延迟关闭
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Transfer of UL41, the gene controlling virion-associated host cell shutoff, between different strains of herpes simplex virus.控制病毒体相关宿主细胞关闭的基因UL41在单纯疱疹病毒不同毒株之间的转移。
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Herpes Simplex Virus 1 Dramatically Alters Loading and Positioning of RNA Polymerase II on Host Genes Early in Infection.单纯疱疹病毒 1 在感染早期显著改变宿主基因上 RNA 聚合酶 II 的加载和定位。
J Virol. 2018 Mar 28;92(8). doi: 10.1128/JVI.02184-17. Print 2018 Apr 15.

引用本文的文献

1
Effect of herpes simplex virus type-1 UL41 gene on the stability of mRNA from the cellular genes: beta-actin, fibronectin, glucose transporter-1, and docking protein, and on virus intraperitoneal pathogenicity to newborn mice.单纯疱疹病毒1型UL41基因对细胞基因β-肌动蛋白、纤连蛋白、葡萄糖转运蛋白1及对接蛋白的mRNA稳定性以及对新生小鼠病毒腹腔致病性的影响。
Virus Genes. 1993 Jun;7(2):133-43. doi: 10.1007/BF01702393.

本文引用的文献

1
Inhibition of host protein synthesis and degradation of cellular mRNAs during infection by influenza and herpes simplex virus.流感病毒和单纯疱疹病毒感染期间宿主蛋白质合成的抑制及细胞mRNA的降解
Mol Cell Biol. 1982 Dec;2(12):1644-8. doi: 10.1128/mcb.2.12.1644-1648.1982.
2
Establishment of dihydrofolate reductase-increased human cell lines and relationship between dihydrofolate reductase levels and gene copy.二氢叶酸还原酶升高的人细胞系的建立以及二氢叶酸还原酶水平与基因拷贝之间的关系
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3
Multiple forms of human dihydrofolate reductase messenger RNA. Cloning and expression in Escherichia coli of their DNA coding sequence.
人类二氢叶酸还原酶信使核糖核酸的多种形式。其DNA编码序列在大肠杆菌中的克隆与表达。
J Mol Biol. 1982 Apr 15;156(3):583-607. doi: 10.1016/0022-2836(82)90268-6.
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The intracellular content of dihydrofolate reductase: possibilities for control and implications for chemotherapy.
Adv Enzyme Regul. 1984;22:15-26. doi: 10.1016/0065-2571(84)90006-2.
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A DNA topoisomerase activity copurifies with the DNA polymerase induced by herpes simplex virus.一种DNA拓扑异构酶活性与单纯疱疹病毒诱导的DNA聚合酶共同纯化。
Biochim Biophys Acta. 1983 Sep 9;740(4):379-89. doi: 10.1016/0167-4781(83)90086-6.
6
Early and delayed shut-off of host protein synthesis in cells infected with herpes simplex virus.单纯疱疹病毒感染细胞中宿主蛋白质合成的早期和延迟关闭
J Gen Virol. 1982 Jul;61 (Pt l):121-5. doi: 10.1099/0022-1317-61-1-121.
7
Structure of replicating herpes simplex virus DNA.单纯疱疹病毒复制型DNA的结构
J Virol. 1981 Aug;39(2):656-60. doi: 10.1128/JVI.39.2.656-660.1981.
8
Herpes simplex virus type 1 HindIII fragment L encodes spliced and complementary mRNA species.单纯疱疹病毒1型HindIII片段L编码剪接的和互补的mRNA种类。
J Virol. 1981 Aug;39(2):559-72. doi: 10.1128/JVI.39.2.559-572.1981.
9
Hybridization of denatured RNA and small DNA fragments transferred to nitrocellulose.变性RNA与转移至硝酸纤维素膜上的小DNA片段的杂交。
Proc Natl Acad Sci U S A. 1980 Sep;77(9):5201-5. doi: 10.1073/pnas.77.9.5201.
10
Activation of the ppp(A2'p)nA system in interferon-treated, herpes simplex virus-infected cells and evidence for novel inhibitors of the ppp(A2'p)nA-dependent RNase.在经干扰素处理的单纯疱疹病毒感染细胞中ppp(A2'p)nA系统的激活以及ppp(A2'p)nA依赖性核糖核酸酶新型抑制剂的证据。
Eur J Biochem. 1984 Aug 15;143(1):165-74. doi: 10.1111/j.1432-1033.1984.tb08355.x.