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伪狂犬病病毒(PRV)早期蛋白0与立即早期蛋白IE180协同激活PRV基因转录,并增强PRV基因组DNA的感染性。

Pseudorabies virus (PRV) early protein 0 activates PRV gene transcription in combination with the immediate-early protein IE180 and enhances the infectivity of PRV genomic DNA.

作者信息

Ono E, Watanabe S, Nikami H, Tasaki T, Kida H

机构信息

Laboratory of Animal Experiments, Hokkaido University, Sapporo, Japan.

出版信息

Vet Microbiol. 1998 Oct;63(2-4):99-107. doi: 10.1016/s0378-1135(98)00236-3.

Abstract

Pseudorabies virus (PRV) early protein 0 (EP0) functions as a transactivator of the viral gene promoters. In transient expression assays employing chloramphenicol acetyl transferase (CAT) reporter constructs, EP0 and the immediate-early protein IE180 act in an additive manner to activate transcription from the thymidine kinase (TK) and glycoprotein G (gG) gene promoters. EP0 enhanced the synthesis of infectious virus in cotransfection experiments with the EP0-expression plasmid and PRV genomic DNA. EP0 was detected by Western blot analysis in the purified virions. These results may indicate that EP0 in the virions acts as an important transactivator to express the immediate-early gene efficiently in the first stage of infection, and IE180 and EP0 expressed after the infection cooperatively activate the early and late gene expression in the later stage of infection.

摘要

伪狂犬病病毒(PRV)早期蛋白0(EP0)作为病毒基因启动子的反式激活因子发挥作用。在使用氯霉素乙酰转移酶(CAT)报告基因构建体的瞬时表达试验中,EP0和即刻早期蛋白IE180以累加方式激活胸苷激酶(TK)和糖蛋白G(gG)基因启动子的转录。在与EP0表达质粒和PRV基因组DNA的共转染实验中,EP0增强了感染性病毒的合成。通过蛋白质免疫印迹分析在纯化的病毒粒子中检测到了EP0。这些结果可能表明,病毒粒子中的EP0在感染的第一阶段作为重要的反式激活因子有效地表达即刻早期基因,而感染后表达的IE180和EP0在感染后期协同激活早期和晚期基因表达。

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