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塞姆利基森林病毒非结构蛋白1的特性及其对病毒复制的干扰。

Properties of non-structural protein 1 of Semliki Forest virus and its interference with virus replication.

作者信息

Kiiver Kaja, Tagen Ingrid, Žusinaite Eva, Tamberg Nele, Fazakerley John K, Merits Andres

机构信息

Estonian Biocentre, Tartu, Estonia.

Institute of Technology, University of Tartu, Tartu, Estonia.

出版信息

J Gen Virol. 2008 Jun;89(Pt 6):1457-1466. doi: 10.1099/vir.0.2008/000299-0.

Abstract

Semliki Forest virus (SFV) non-structural protein 1 (nsP1) is a major component of the virus replicase complex. It has previously been studied in cells infected with virus or using transient or stable expression systems. To extend these studies, tetracycline-inducible stable cell lines expressing SFV nsP1 or its palmitoylation-negative mutant (nsP16D) were constructed. The levels of protein expression and the subcellular localization of nsP1 in induced cells were similar to those in virus-infected cells. The nsP1 expressed by stable, inducible cell lines or by SFV-infected HEK293 T-REx cells was a stable protein with a half-life of approximately 5 h. In contrast to SFV infection, induction of nsP1 expression had no detectable effect on cellular transcription, translation or viability. Induction of expression of nsP1 or nsP16D interfered with multiplication of SFV, typically resulting in a 5-10-fold reduction in virus yields. This reduction was not due to a decrease in the number of infected cells, indicating that nsP1 expression does not block virus entry or initiation of replication. Expression of nsP1 interfered with virus genomic RNA synthesis and delayed accumulation of viral subgenomic RNA translation products. Expression of nsP1 with a mutation in the palmitoylation site reduced synthesis of genomic and subgenomic RNAs and their products of translation, and this effect did not resolve with time. These results are in agreement with data published previously, suggesting a role for nsP1 in genomic RNA synthesis.

摘要

塞姆利基森林病毒(SFV)非结构蛋白1(nsP1)是病毒复制酶复合物的主要成分。此前已在感染病毒的细胞中或使用瞬时或稳定表达系统对其进行过研究。为了扩展这些研究,构建了表达SFV nsP1或其棕榈酰化阴性突变体(nsP16D)的四环素诱导稳定细胞系。诱导细胞中nsP1的蛋白表达水平和亚细胞定位与病毒感染细胞中的相似。由稳定的诱导细胞系或SFV感染的HEK293 T-REx细胞表达的nsP1是一种稳定蛋白,半衰期约为5小时。与SFV感染不同,诱导nsP1表达对细胞转录、翻译或活力没有可检测到的影响。诱导nsP1或nsP16D表达会干扰SFV的增殖,通常导致病毒产量降低5至10倍。这种降低不是由于感染细胞数量的减少,表明nsP1表达不会阻止病毒进入或复制起始。nsP1的表达会干扰病毒基因组RNA的合成,并延迟病毒亚基因组RNA翻译产物的积累。棕榈酰化位点发生突变的nsP1的表达会降低基因组和亚基因组RNA及其翻译产物的合成,并且这种影响不会随时间消除。这些结果与先前发表的数据一致,表明nsP1在基因组RNA合成中起作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0938/2886950/a7649f817e26/1457fig1.jpg

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