Nonoyama M, Tanaka A, Silver S, Glaser R
IARC Sci Publ (1971). 1978(24 Pt 1):559-63.
Expression of latent Epstein-Barr virus genomes in lymphoblastoid cells and somatic-cell hybrid of Burkitt's lymphoblastoid cells has been studied. IUDR treatment induced the formation of early antigen (EA), virus capsid antigen (VCA) and virus DNA replication in D98/Raji and D98/HR-1 cells whereas only EA was induced in Raji cells. HR-1 clone No. 9 did not respond to IUDR treatment. The pattern of transcription of virus genomes in these cell lines without IUDR treatment was uniform with 20--25% of virus DNA transcribed. IUDR treatment enhanced the transcription of virus DNA to 50% in D98/Raji, D98/HR-1 and Raji cells but no enhancement of virus genome transcription was observed in HR-1 clone No. 9 The amount of virus RNA in the cells calculated from DNA-RNA hybridization kinetics was found to be proportional to the number of virus genomes per cell indicating that every copy of virus DNA in these cells is actively transcribed.
对潜伏性爱泼斯坦-巴尔病毒基因组在淋巴母细胞以及伯基特淋巴瘤母细胞的体细胞杂种中的表达进行了研究。碘苷(IUDR)处理诱导D98/Raji和D98/HR-1细胞中早期抗原(EA)、病毒衣壳抗原(VCA)的形成以及病毒DNA复制,而拉吉(Raji)细胞中仅诱导出EA。HR-1第9号克隆对碘苷处理无反应。在未经碘苷处理的这些细胞系中,病毒基因组的转录模式是一致的,20%-25%的病毒DNA被转录。碘苷处理使D98/Raji、D98/HR-1和拉吉细胞中病毒DNA的转录增强至50%,但在HR-1第9号克隆中未观察到病毒基因组转录增强。根据DNA-RNA杂交动力学计算,细胞中病毒RNA量与每个细胞中病毒基因组数量成正比,表明这些细胞中病毒DNA的每个拷贝都在活跃转录。