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Cell Cycle Dysregulation by Human Cytomegalovirus: Influence of the Cell Cycle Phase at the Time of Infection and Effects on Cyclin Transcription

机译:人巨细胞病毒引起的细胞周期失调:感染时细胞周期阶段的影响以及对细胞周期蛋白转录的影响

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摘要

Human cytomegalovirus (HCMV) infection inhibits cell cycle progression and alters the expression of cyclins E, A, and B (F. M. Jault, J.-M. Jault, F. Ruchti, E. A. Fortunato, C. Clark, J. Corbeil, D. D. Richman, and D. H. Spector, J. Virol. 69:6697–6704, 1995). In this study, we examined cell cycle progression, cyclin gene expression, and early viral events when the infection was initiated at different points in the cell cycle (G0, G1, and S). In all cases, infection led to cell cycle arrest. Cells infected in G0 or G1 phase also showed a complete or partial absence, respectively, of cellular DNA synthesis at a time when DNA synthesis occurred in the corresponding mock-infected cells. In contrast, when cells were infected near or during S phase, many cells were able to pass through S phase and undergo mitosis prior to cell cycle arrest. S-phase infection also produced a delay in the appearance of the viral cytopathic effect and in the synthesis of immediate-early and early proteins. Labeling of cells with bromodeoxyuridine immediately prior to HCMV infection in S phase revealed that viral protein expression occurred primarily in cells which were not engaged in DNA synthesis at the time of infection. The viral-mediated induction of cyclin E, maintenance of cyclin-B protein levels, and inhibitory effects on the accumulation of cyclin A were not significantly affected when infection occurred during different phases of the cell cycle (G0, G1, and S). However, there was a delay in the observed inhibition of cyclin A in cells infected during S phase. This finding was in accord with the pattern of cell cycle progression and delay in viral gene expression associated with S-phase infection. Analysis of the mRNA revealed that the effects of the virus on cyclin E and cyclin A, but not on cyclin B, were primarily at the transcriptional level.
机译:人巨细胞病毒(HCMV)感染抑制细胞周期进程并改变细胞周期蛋白E,A和B的表达(FM Jault,J.-M。Jault,F。Ruchti,EA Fortunato,C。Clark,J.Corbeil,DD Richman和DH Spector,J. Virol。69:6697–6704,1995)。在这项研究中,我们检查了在细胞周期的不同点(G0,G1和S)开始感染时的细胞周期进程,细胞周期蛋白基因表达和早期病毒事件。在所有情况下,感染都会导致细胞周期停滞。在相应的模拟感染细胞中发生DNA合成时,G0或G1期感染的细胞也分别显示出细胞DNA合成的完全或部分缺失。相反,当细胞在S期附近或期间感染时,许多细胞能够通过S期并在细胞周期停滞之前经历有丝分裂。 S期感染还导致病毒细胞病变作用的出现以及即早和早蛋白的合成的延迟。在S期HCMV感染前立即用溴脱氧尿苷标记细胞,表明病毒蛋白表达主要发生在感染时未参与DNA合成的细胞中。当在细胞周期的不同阶段(G0,G1和S)发生感染时,病毒介导的细胞周期蛋白E诱导,细胞周期蛋白B蛋白水平的维持以及对细胞周期蛋白A积累的抑制作用不会受到明显影响。但是,在S期感染的细胞中观察到的细胞周期蛋白A抑制作用有所延迟。这一发现与细胞周期进展的模式以及与S期感染相关的病毒基因表达的延迟相一致。对mRNA的分析表明,病毒对细胞周期蛋白E和细胞周期蛋白A的影响主要在转录水平,而对细胞周期蛋白B没有影响。

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