Tsuchida N, Green M
J Virol. 1974 Sep;14(3):587-91. doi: 10.1128/JVI.14.3.587-591.1974.
The size and quantity of virus-specific RNA in five non-virus-producing mouse cells transformed by the Moloney isolate of murine sarcoma virus (MSV) was determined. Hybridization of RNA from transformed cells with the [(3)H]DNA product of the RNA-directed DNA polymerase of the murine sarcoma-leukemia virus was used to detect and quantitate virus-specific RNA. The amount of virus-specific RNA in non-virus-producing cells was less than one-sixth of that found in virus-producing cells. A striking correlation was found between the amount of intracellular virus-specific RNA and the degree of agglutination by conconavalin A previously reported for the four non-virus-producing NIH/3T3 cell lines (Salzberg and Green, 1974). A major RNA subunit sedimenting at 26 to 28S was detected in all five MSV-transformed non-virus-producing cells. This could represent the RNA genome of defective MSV.
测定了由莫洛尼氏鼠肉瘤病毒(MSV)分离株转化的五个不产生病毒的小鼠细胞中病毒特异性RNA的大小和数量。用来自转化细胞的RNA与鼠肉瘤-白血病病毒的RNA指导的DNA聚合酶的[³H]DNA产物进行杂交,以检测和定量病毒特异性RNA。不产生病毒的细胞中病毒特异性RNA的量不到产生病毒的细胞中所发现量的六分之一。先前报道的四种不产生病毒的NIH/3T3细胞系中,细胞内病毒特异性RNA的量与刀豆球蛋白A的凝集程度之间存在显著相关性(萨尔茨伯格和格林,1974年)。在所有五个MSV转化的不产生病毒的细胞中都检测到了一个沉降系数为26至28S的主要RNA亚基。这可能代表缺陷型MSV的RNA基因组。