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单纯疱疹病毒的插入突变体具有糖蛋白D基因的重复,并表达两种不同形式的糖蛋白D。

Insertion mutants of herpes simplex virus have a duplication of the glycoprotein D gene and express two different forms of glycoprotein D.

作者信息

Gibson M G, Spear P G

出版信息

J Virol. 1983 Nov;48(2):396-404. doi: 10.1128/JVI.48.2.396-404.1983.

DOI:10.1128/JVI.48.2.396-404.1983
PMID:6312097
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC255364/
Abstract

We produced insertion mutants of herpes simplex virus (HSV) that contain two functional copies of genes encoding different forms of glycoprotein D (gD). These viruses have the gene for HSV type 2 (HSV-2) gD at the normal locus and the gene for HSV-1 gD inserted into the thymidine kinase locus. Results of immunoprecipitation experiments done with monoclonal antibodies revealed that both gD genes were expressed by these viruses, regardless of orientation of the inserted HSV-1 gD gene, and that maximal synthesis of both glycoproteins depended on viral DNA replication. This apparently normal expression of the inserted HSV-1 gD gene was from a DNA fragment (SacI fragment, 0.906 to 0.924 map units) containing nucleotide sequences extending from approximately 400 base pairs upstream of the 5' end of the gD mRNA to about 200 base pairs upstream of the 3' end. The glycoproteins expressed from both genes were incorporated into the surfaces of infected cells. Electrophoretic analyses of purified virions and neutralization studies suggest that both glycoproteins were also incorporated into virions. This nonpreferential utilization of both gene products makes these viruses ideal strains for the generation and characterization of a variety of mutations.

摘要

我们构建了单纯疱疹病毒(HSV)插入突变体,其含有编码不同形式糖蛋白D(gD)的两个功能基因拷贝。这些病毒在正常位点具有2型单纯疱疹病毒(HSV-2)gD基因,而1型单纯疱疹病毒(HSV-1)gD基因插入到胸苷激酶位点。用单克隆抗体进行的免疫沉淀实验结果表明,无论插入的HSV-1 gD基因的方向如何,这两种gD基因均由这些病毒表达,并且两种糖蛋白的最大合成均依赖于病毒DNA复制。插入的HSV-1 gD基因这种明显正常的表达来自一个DNA片段(SacI片段,0.906至0.924图谱单位),其核苷酸序列从gD mRNA 5'端上游约400个碱基对延伸至3'端上游约200个碱基对。从这两个基因表达的糖蛋白都整合到受感染细胞的表面。对纯化病毒粒子的电泳分析和中和研究表明,这两种糖蛋白也整合到病毒粒子中。这两种基因产物的非优先利用使得这些病毒成为产生和鉴定各种突变的理想毒株。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b77e/255364/2506ad5f7260/jvirol00140-0074-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b77e/255364/dd601aa6b11d/jvirol00140-0071-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b77e/255364/3e257f9ec15e/jvirol00140-0072-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b77e/255364/3d6bae44fe0e/jvirol00140-0072-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b77e/255364/ba3c72ee6811/jvirol00140-0073-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b77e/255364/e7fc6f2e905a/jvirol00140-0073-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b77e/255364/2506ad5f7260/jvirol00140-0074-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b77e/255364/dd601aa6b11d/jvirol00140-0071-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b77e/255364/3e257f9ec15e/jvirol00140-0072-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b77e/255364/3d6bae44fe0e/jvirol00140-0072-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b77e/255364/ba3c72ee6811/jvirol00140-0073-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b77e/255364/e7fc6f2e905a/jvirol00140-0073-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b77e/255364/2506ad5f7260/jvirol00140-0074-a.jpg

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Inhibition of DNA polymerase from herpes simplex virus-infected wi-38 cells by phosphonoacetic Acid.膦甲酸对单纯疱疹病毒感染的WI-38细胞中DNA聚合酶的抑制作用。
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Inhibition of herpes simplex virus replication by phosphonoacetic acid.膦甲酸钠对单纯疱疹病毒复制的抑制作用。
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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.
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The control of herpes simplex virus type-1 late gene transcription: a 'TATA-box'/cap site region is sufficient for fully efficient regulated activity.单纯疱疹病毒1型晚期基因转录的调控:一个“TATA盒”/帽位点区域足以实现完全有效的调控活性。
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Enhanced rate of conversion or recombination of markers within a region of unique sequence in the herpes simplex virus genome.单纯疱疹病毒基因组中独特序列区域内标记物的转化或重组速率增强。
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Identification of a new glycoprotein of herpes simplex virus type 1 and genetic mapping of the gene that codes for it.1型单纯疱疹病毒一种新糖蛋白的鉴定及其编码基因的遗传定位。
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J Virol. 1985 Dec;56(3):757-66. doi: 10.1128/JVI.56.3.757-766.1985.
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Novel rearrangements of herpes simplex virus DNA sequences resulting from duplication of a sequence within the unique region of the L component.由L组分独特区域内的一个序列重复导致的单纯疱疹病毒DNA序列的新型重排。
J Virol. 1985 Feb;53(2):456-61. doi: 10.1128/JVI.53.2.456-461.1985.
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The contribution of cysteine residues to antigenicity and extent of processing of herpes simplex virus type 1 glycoprotein D.半胱氨酸残基对单纯疱疹病毒1型糖蛋白D抗原性及加工程度的作用
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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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Characterization of the herpes simplex virus type 1 glycoprotein D mRNA and expression of this protein in Xenopus oocytes.单纯疱疹病毒1型糖蛋白D mRNA的特性及其在非洲爪蟾卵母细胞中的蛋白表达
Nucleic Acids Res. 1983 Mar 11;11(5):1507-22. doi: 10.1093/nar/11.5.1507.
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An immunologically active chimaeric protein containing herpes simplex virus type 1 glycoprotein D.一种含有1型单纯疱疹病毒糖蛋白D的具有免疫活性的嵌合蛋白。
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Structural features of the herpes simplex virus alpha gene 4, 0, and 27 promoter-regulatory sequences which confer alpha regulation on chimeric thymidine kinase genes.单纯疱疹病毒α基因4、0和27启动子调控序列的结构特征,这些序列赋予嵌合胸苷激酶基因α调控作用。
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Expression of herpes simplex virus glycoprotein C from a DNA fragment inserted into the thymidine kinase gene of this virus.单纯疱疹病毒糖蛋白C在插入该病毒胸苷激酶基因的DNA片段中的表达。
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Glycoproteins of herpes simplex virus type 2 as defined by monoclonal antibodies.由单克隆抗体定义的2型单纯疱疹病毒糖蛋白
J Virol. 1982 Oct;44(1):344-55. doi: 10.1128/JVI.44.1.344-355.1982.
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Regulation of alpha genes of herpes simplex virus: the alpha 27 gene promoter-thymidine kinase chimera is positively regulated in converted L cells.单纯疱疹病毒α基因的调控:α27基因启动子-胸苷激酶嵌合体在转化的L细胞中受到正调控。
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Herpes simplex virus type-1 glycoprotein D gene: nucleotide sequence and expression in Escherichia coli.单纯疱疹病毒1型糖蛋白D基因:核苷酸序列及其在大肠杆菌中的表达
Science. 1982 Oct 22;218(4570):381-4. doi: 10.1126/science.6289440.