Lowy D R, Rowe W P, Teich N, Hartley J W
Science. 1971 Oct 8;174(4005):155-6. doi: 10.1126/science.174.4005.155.
Cells of embryos of the high leukemic mouse strain AKR can be grown in culture as virus-negative cell lines. However, these lines and clonal sublines uniformly have the capacity to initiate synthesis of murine leukemia virus. Exposure of the cells to 5-iododeoxyuridine or 5-bromodeoxyuridine induced synthesis of virus in as high as 0.1 to 0.5 percent of the cells; many of the cells were producing virus as soon as 3 days after initiation of treatment. Induction of virus by these drugs is several orders of magnitude greater than that obtained with any other treatment tested. These studies indicate that the full genome of murine leukemia virus is present in an unexpressed form in all AKR cells and provide a potentially powerful technique for activating leukemia virus genomes in other cell systems.
高白血病小鼠品系AKR胚胎的细胞可以在培养中作为病毒阴性细胞系生长。然而,这些细胞系和克隆亚系均具有启动鼠白血病病毒合成的能力。将细胞暴露于5-碘脱氧尿苷或5-溴脱氧尿苷可诱导高达0.1%至0.5%的细胞合成病毒;许多细胞在开始治疗后3天就开始产生病毒。这些药物诱导病毒的能力比其他任何测试过的治疗方法高出几个数量级。这些研究表明,鼠白血病病毒的完整基因组以未表达的形式存在于所有AKR细胞中,并为激活其他细胞系统中的白血病病毒基因组提供了一种潜在的强大技术。