Department of Medical Biology, Faculty of Medicine, University of Szeged, Somogyi B. st. 4., Szeged, H-6720, Hungary.
Gene. 2012 Feb 10;493(2):235-42. doi: 10.1016/j.gene.2011.11.049. Epub 2011 Dec 9.
Real-time RT-PCR analysis was applied to evaluate the impact of deletion of the early protein 0 (EP0) gene of pseudorabies virus (PRV) on the global expression of the viral transcripts during lytic infection in cultured porcine kidney cells. Our analysis showed that EP0 exerted an inhibitory effect on the transcription of the PRV genes in the early stage of infection, and alternating stimulatory and inhibitory effects on the viral gene expressions in the late stage of infection. The data also suggested that a general function of EP0 might be to reverse the kinetics of expression of early viral genes. We also observed that EP0 facilitated the development of correlations in the transcription kinetics between the immediate early 180 gene and the PRV transcripts, indicating that a major function of EP0 could be to modify the effects of the IE180 protein on the PRV transcriptome.
实时 RT-PCR 分析被应用于评估猪伪狂犬病病毒(PRV)早期蛋白 0(EP0)基因缺失对培养的猪肾细胞中裂解感染时病毒转录物的全球表达的影响。我们的分析表明,EP0 在感染的早期阶段对 PRV 基因的转录具有抑制作用,并且在感染的晚期阶段对病毒基因的表达具有交替的刺激和抑制作用。数据还表明,EP0 的一个普遍功能可能是逆转早期病毒基因表达的动力学。我们还观察到,EP0 促进了即刻早期 180 基因和 PRV 转录物之间转录动力学相关性的发展,这表明 EP0 的主要功能之一可能是修饰 IE180 蛋白对 PRV 转录组的影响。