Bacheler L, Jaenisch R, Fan H
J Virol. 1979 Mar;29(3):899-906. doi: 10.1128/JVI.29.3.899-906.1979.
Permanent, non-virus-producing cell lines have been established from a mouse embryo carrying an endogenous, genetically transmitted Moloney murine leukemia virus (M-MuLV) genome. These cells carry the M-MuLV genome, as demonstrated by hybridization of cellular DNA to M-MuLV complementary DNA, but do not express it at the levels of virus production, accumulation of intracellular viral p30, or M-MuLV-specific RNA. Treatment with bromodeoxyuridine (50 microgram/ml for 24 h) resulted in induction of XC-positive NB-tropic virus, although only a small fraction of the cells released virus (less than 0.1% after 48 h). Immunofluorescent staining and flow microfluorometry indicated that a wave of p30 accumulation occurs in the induced cells, with a maximum at 24 to 48 h after the addition of bromodeoxyuridine. Furthermore, most, if not all, cells were induced to produce p30 protein. Similar kinetics were found for the accumulation of M-MuLV-specific RNA in the cytoplasm of induced cells. This rapid induction of virus expression in a majority of cells was dependent on the presence of the M-MuLV genome and probably represents primarily the expression of this endogenous virus since induction was not observed in cells similarly derived from a sibling embryo lacking the M-MuLV genome.
已从携带内源性、经基因传递的莫洛尼鼠白血病病毒(M-MuLV)基因组的小鼠胚胎中建立了永久性的、不产生病毒的细胞系。这些细胞携带M-MuLV基因组,这通过细胞DNA与M-MuLV互补DNA的杂交得以证明,但它们在病毒产生水平、细胞内病毒p30的积累或M-MuLV特异性RNA水平上均不表达。用溴脱氧尿苷(50微克/毫升,处理24小时)处理导致诱导出XC阳性的嗜NB病毒,尽管只有一小部分细胞释放病毒(48小时后不到0.1%)。免疫荧光染色和流式细胞荧光测定表明,在诱导细胞中出现了一波p30积累,在添加溴脱氧尿苷后24至48小时达到最大值。此外,大多数(如果不是全部)细胞被诱导产生p30蛋白。在诱导细胞的细胞质中,M-MuLV特异性RNA的积累也发现了类似的动力学。大多数细胞中病毒表达的这种快速诱导依赖于M-MuLV基因组的存在,并且可能主要代表这种内源性病毒的表达,因为在来自缺乏M-MuLV基因组的同胞胚胎的类似细胞中未观察到诱导现象。