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单纯疱疹病毒1型基因组的转录和遗传分析:坐标0.29至0.45。

Transcriptional and genetic analyses of the herpes simplex virus type 1 genome: coordinates 0.29 to 0.45.

作者信息

Holland L E, Sandri-Goldin R M, Goldin A L, Glorioso J C, Levine M

出版信息

J Virol. 1984 Mar;49(3):947-59. doi: 10.1128/JVI.49.3.947-959.1984.

DOI:10.1128/JVI.49.3.947-959.1984
PMID:6199514
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC255557/
Abstract

We have constructed a map of the genes encoded by a 23,000-nucleotide-pair region of herpes simplex virus type 1. This region, defined by the three adjacent EcoRI fragments N (map coordinates 0.298 to 0.315), F (0.315 to 0.421), and M (0.421 to 0.448), has previously been shown by genetic analysis to contain the genes for thymidine kinase, nucleocapsid protein p40, glycoprotein B, DNA-binding protein, and DNA polymerase. We report the identification and mapping of RNAs defining 13 viral genes encoded by the region 0.298 to 0.448. The transcriptional pattern shows families of overlapping messages, similar to those observed in other regions of the viral genome. We also isolated mutants representing four distinct complementation groups and physically mapped several of the mutations to regions within EcoRI fragment F by marker rescue. Mutations representing complementation groups 1-9 (glycoprotein B), 1-1 (DNA-binding protein), and 1-3 (DNA polymerase) were mapped to coordinates 0.361 to 0.368 to 0.411, and 0.411 to 0.421, respectively. A fourth previously undefined complementation group was mapped to the region between glycoprotein B and DNA-binding protein. Comparing the transcription mapping with marker rescue data suggests that the genes for glycoprotein B, DNA-binding protein, DNA polymerase, and nucleocapsid protein p40 are expressed as 3.3-, 4.2-, 4.3- or 4.2- or both, and 2.4-kilobase mRNAs, respectively.

摘要

我们构建了一张单纯疱疹病毒1型23000个核苷酸对区域所编码基因的图谱。该区域由三个相邻的EcoRI片段N(图谱坐标0.298至0.315)、F(0.315至0.421)和M(0.421至0.448)界定,先前通过遗传分析已表明其包含胸苷激酶、核衣壳蛋白p40、糖蛋白B、DNA结合蛋白和DNA聚合酶的基因。我们报告了对定义该0.298至0.448区域所编码的13个病毒基因的RNA的鉴定和定位。转录模式显示出重叠信息家族,类似于在病毒基因组其他区域观察到的情况。我们还分离出代表四个不同互补组的突变体,并通过标记拯救将其中几个突变物理定位到EcoRI片段F内的区域。代表互补组1 - 9(糖蛋白B)、1 - 1(DNA结合蛋白)和1 - 3(DNA聚合酶)的突变分别定位到坐标0.361至0.368至0.411以及0.411至0.421。第四个先前未定义的互补组定位到糖蛋白B和DNA结合蛋白之间的区域。将转录图谱与标记拯救数据进行比较表明,糖蛋白B、DNA结合蛋白、DNA聚合酶和核衣壳蛋白p40的基因分别以3.3、4.2、4.3或4.2或两者以及2.4千碱基的mRNA形式表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2779/255557/ddf8b1734cf6/jvirol00138-0329-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2779/255557/22956927eb55/jvirol00138-0326-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2779/255557/ddf8b1734cf6/jvirol00138-0329-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2779/255557/22956927eb55/jvirol00138-0326-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2779/255557/ddf8b1734cf6/jvirol00138-0329-a.jpg

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本文引用的文献

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Characterization of the major mRNAs transcribed from the genes for glycoprotein B and DNA-binding protein ICP8 of herpes simplex virus type 1.单纯疱疹病毒1型糖蛋白B和DNA结合蛋白ICP8基因转录的主要mRNA的特性分析
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Herpes simplex virus 1 microRNAs expressed abundantly during latent infection are not essential for latency in mouse trigeminal ganglia.单纯疱疹病毒 1 微 RNA 在潜伏感染期间大量表达,但对于小鼠三叉神经节潜伏感染并非必需。
Virology. 2011 Sep 1;417(2):239-47. doi: 10.1016/j.virol.2011.06.027. Epub 2011 Jul 23.
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UL31 of herpes simplex virus 1 is necessary for optimal NF-kappaB activation and expression of viral gene products.单纯疱疹病毒 1 的 UL31 对于 NF-κB 的最佳激活和病毒基因产物的表达是必要的。
J Virol. 2011 May;85(10):4947-53. doi: 10.1128/JVI.00068-11. Epub 2011 Mar 9.
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Construction and characterization of a herpes simplex virus type I recombinant expressing green fluorescent protein: acute phase replication and reactivation in mice.表达绿色荧光蛋白的I型单纯疱疹病毒重组体的构建与鉴定:小鼠急性期复制与再激活
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Linker insertion mutations in the herpes simplex virus type 1 UL28 gene: effects on UL28 interaction with UL15 and UL33 and identification of a second-site mutation in the UL15 gene that suppresses a lethal UL28 mutation.单纯疱疹病毒1型UL28基因中的接头插入突变:对UL28与UL15和UL33相互作用的影响以及UL15基因中一个抑制致死性UL28突变的第二位点突变的鉴定。
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Fine mapping and molecular cloning of mutations in the herpes simplex virus DNA polymerase locus.单纯疱疹病毒DNA聚合酶基因座突变的精细定位与分子克隆
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Thermolabile in vivo DNA-binding activity associated with a protein encoded by mutants of herpes simplex virus type 1.与单纯疱疹病毒1型突变体编码的一种蛋白质相关的体内热不稳定DNA结合活性。
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Physical mapping of the mutation in an antigenic variant of herpes simplex virus type 1 by use of an immunoreactive plaque assay.通过免疫反应性噬斑测定法对单纯疱疹病毒1型抗原变异体中的突变进行物理图谱分析。
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Identification and characterization of a herpes simplex virus gene product required for encapsidation of virus DNA.单纯疱疹病毒DNA包装所需病毒基因产物的鉴定与特性分析。
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