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RNA按照其细胞内浓度的比例被包装进人巨细胞病毒病毒粒子中。

RNAs are packaged into human cytomegalovirus virions in proportion to their intracellular concentration.

作者信息

Terhune Scott S, Schröer Jörg, Shenk Thomas

机构信息

Department of Molecular Biology, Princeton University, Princeton, NJ 08544-1014, USA.

出版信息

J Virol. 2004 Oct;78(19):10390-8. doi: 10.1128/JVI.78.19.10390-10398.2004.

Abstract

The assembly of human cytomegalovirus (HCMV) virions is a complex process and involves the incorporation of viral transcripts. These RNAs are delivered to the newly infected cells and have the potential to be translated in the absence of HCMV gene expression. We have quantified the relative amount of RNAs in HCMV virions and infected cells with real-time reverse transcription-PCR and observed that viral and cellular RNAs are packaged in proportion to the amount of RNA within the cell at the time of assembly. To determine whether cis elements influenced RNA packaging, we constructed a recombinant HCMV mutant virus that expressed the yellow fluorescence protein (YFP) gene fused to the virion RNA UL21.5. We also constructed a mutant virus in which the UL21.5 transcription unit was replaced with the YFP gene. YFP RNA was incorporated into both viruses, indicating that RNA is incorporated in the absence of a virus-specific signal motif. Furthermore, with in situ hybridization, packaged transcripts were observed throughout the cytoplasm of the infected cells, including the site of virus assembly. Several proteins that nonspecifically interact with RNA, including the tegument protein pp28, were found within HCMV virions. These studies demonstrate that both viral and cellular RNAs are nonspecifically incorporated into HCMV, potentially through interactions with several virion proteins.

摘要

人类巨细胞病毒(HCMV)病毒粒子的组装是一个复杂的过程,涉及病毒转录本的掺入。这些RNA被递送至新感染的细胞,并有可能在没有HCMV基因表达的情况下进行翻译。我们用实时逆转录PCR对HCMV病毒粒子和感染细胞中的RNA相对量进行了定量,观察到病毒RNA和细胞RNA的包装比例与组装时细胞内RNA的量成比例。为了确定顺式元件是否影响RNA包装,我们构建了一种重组HCMV突变病毒,该病毒表达与病毒粒子RNA UL21.5融合的黄色荧光蛋白(YFP)基因。我们还构建了一种突变病毒,其中UL21.5转录单元被YFP基因取代。YFP RNA被掺入两种病毒中,表明RNA在没有病毒特异性信号基序的情况下被掺入。此外,通过原位杂交,在感染细胞的整个细胞质中观察到包装的转录本,包括病毒组装位点。在HCMV病毒粒子中发现了几种与RNA非特异性相互作用的蛋白质,包括包膜蛋白pp28。这些研究表明,病毒RNA和细胞RNA都可能通过与几种病毒粒子蛋白的相互作用而非特异性地掺入HCMV。

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