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单纯疱疹病毒1感染细胞中介导α基因诱导的病毒体蛋白与其顺式位点的结合需要细胞蛋白。

Binding of the virion protein mediating alpha gene induction in herpes simplex virus 1-infected cells to its cis site requires cellular proteins.

作者信息

McKnight J L, Kristie T M, Roizman B

机构信息

Marjorie B. Kovler Viral Oncology Laboratories, University of Chicago, IL 60637.

出版信息

Proc Natl Acad Sci U S A. 1987 Oct;84(20):7061-5. doi: 10.1073/pnas.84.20.7061.

DOI:10.1073/pnas.84.20.7061
PMID:2823252
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC299229/
Abstract

In herpes simplex virus 1-infected cells, the transcription of alpha genes, the first set of genes to be expressed, is induced by a virion component, the alpha-trans-induction factor, and requires a cis site. Homologs of the cis site are present in the promoter-regulatory domains of all alpha genes and bind two cellular proteins designated as alpha H1 and alpha H2-alpha H3. We report that alpha-trans-induction factor, synthesized in vitro or present in nuclear extracts of infected cells, forms complexes with viral DNA fragments containing its cis-acting site only in the presence of cellular proteins and only under conditions that also enable the binding of the alpha H1 protein to the DNA. The induction of alpha genes by alpha-trans-induction factor appears, therefore, to be mediated by the interaction of the viral protein with cellular proteins at its cis-acting site.

摘要

在单纯疱疹病毒1感染的细胞中,α基因是首批表达的基因,其转录由一种病毒体成分α反式诱导因子所诱导,并且需要一个顺式位点。顺式位点的同源物存在于所有α基因的启动子调控区域,并与两种被称为αH1和αH2 - αH3的细胞蛋白结合。我们报告称,在体外合成或存在于感染细胞的核提取物中的α反式诱导因子,仅在细胞蛋白存在的情况下,并且仅在能使αH1蛋白与DNA结合的条件下,才会与含有其顺式作用位点的病毒DNA片段形成复合物。因此,α反式诱导因子对α基因的诱导似乎是由病毒蛋白在其顺式作用位点与细胞蛋白的相互作用介导的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ab6/299229/77520fc6a2db/pnas00335-0111-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ab6/299229/63f9c10ce6cf/pnas00335-0109-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ab6/299229/eae1a2e8e3fa/pnas00335-0110-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ab6/299229/272453fc7e70/pnas00335-0111-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ab6/299229/77520fc6a2db/pnas00335-0111-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ab6/299229/63f9c10ce6cf/pnas00335-0109-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ab6/299229/eae1a2e8e3fa/pnas00335-0110-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ab6/299229/272453fc7e70/pnas00335-0111-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ab6/299229/77520fc6a2db/pnas00335-0111-b.jpg

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Binding of the virion protein mediating alpha gene induction in herpes simplex virus 1-infected cells to its cis site requires cellular proteins.单纯疱疹病毒1感染细胞中介导α基因诱导的病毒体蛋白与其顺式位点的结合需要细胞蛋白。
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Accurate transcription initiation by RNA polymerase II in a soluble extract from isolated mammalian nuclei.从分离的哺乳动物细胞核的可溶性提取物中,RNA聚合酶II进行准确的转录起始。
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miRNAs Targeting ICP4 and Delivered to Susceptible Cells in Exosomes Block HSV-1 Replication in a Dose-Dependent Manner.miRNAs 靶向 ICP4 并通过外泌体递送至易感细胞以剂量依赖方式阻断 HSV-1 复制。
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PUM1 is a biphasic negative regulator of innate immunity genes by suppressing LGP2.PUM1 通过抑制 LGP2 来双向调控先天免疫基因。
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De Novo Herpes Simplex Virus VP16 Expression Gates a Dynamic Programmatic Transition and Sets the Latent/Lytic Balance during Acute Infection in Trigeminal Ganglia.新生单纯疱疹病毒VP16表达调控动态程序性转变并在三叉神经节急性感染期间设定潜伏/裂解平衡。
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PML plays both inimical and beneficial roles in HSV-1 replication.早幼粒细胞白血病蛋白在单纯疱疹病毒1型复制中发挥着有害和有益的双重作用。
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miR-H28 and miR-H29 expressed late in productive infection are exported and restrict HSV-1 replication and spread in recipient cells.在 productive 感染后期表达的 miR-H28 和 miR-H29 被输出,并限制单纯疱疹病毒 1 型在受体细胞中的复制和传播。
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Inhibition of O-Linked N-Acetylglucosamine Transferase Reduces Replication of Herpes Simplex Virus and Human Cytomegalovirus.O-连接的N-乙酰葡糖胺转移酶的抑制作用降低单纯疱疹病毒和人巨细胞病毒的复制。
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The 3 facets of regulation of herpes simplex virus gene expression: A critical inquiry.单纯疱疹病毒基因表达调控的三个方面:批判性探究
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在单纯疱疹病毒1型α基因调控域内,将定义基础表达的序列与赋予α基因识别能力的序列分开。
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Differentiation between alpha promoter and regulator regions of herpes simplex virus 1: the functional domains and sequence of a movable alpha regulator.单纯疱疹病毒1型α启动子与调控区域的区分:一个可移动α调控因子的功能结构域与序列
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A gel electrophoresis method for quantifying the binding of proteins to specific DNA regions: application to components of the Escherichia coli lactose operon regulatory system.一种用于定量蛋白质与特定DNA区域结合的凝胶电泳方法:应用于大肠杆菌乳糖操纵子调控系统的组分
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