Kelly R K, Butel J S
Arch Virol. 1975;48(4):279-87. doi: 10.1007/BF01317426.
The initial steps in the DNA-transfer, or transfection, method of virus rescue were characterized using primary green monkey (GMK) cells exposed to SV40-transformed mouse (SV-3T3) cell DNA in the presence of 1 mg/ml DEAE-dextran. When large amounts (10-50mug) of high molecular weight DNA (greater than 10(7) daltons) were inoculated onto 10(6) GMK cells, usually less than 1 mug became cell-associated. DNA fragmented to a size of 1-3 X 10(6) daltons was bound more efficiently by the recipient cells, but generally only 5-10 per cent of the inoculum (representing 1-4 mug) was taken up. Approximately 50 per cent of the cell-associated DNA had penetrated to a DNase-resistant state by the end of the 30-minute incubation period. The effect of the size of thr transformed cell DNA molecule on the recovery of SV40 in transfection experiments was investigated. The trend appeared to be that rescue was more efficient with the larger molecular weight samples.
在DNA转移(即转染)病毒拯救方法的初始步骤中,使用原代绿猴(GMK)细胞进行了表征,这些细胞在1mg/ml 二乙氨基乙基葡聚糖存在的情况下暴露于SV40转化的小鼠(SV-3T3)细胞DNA。当将大量(10 - 50μg)高分子量DNA(大于10⁷道尔顿)接种到10⁶个GMK细胞上时,通常只有不到1μg与细胞结合。片段化至1 - 3×10⁶道尔顿大小的DNA被受体细胞更有效地结合,但一般来说接种物中只有5 - 10%(相当于1 - 4μg)被摄取。在30分钟的孵育期结束时,约50%与细胞结合的DNA已渗透到对DNA酶有抗性的状态。研究了转化细胞DNA分子大小对转染实验中SV40拯救效率的影响。趋势似乎是分子量较大的样品拯救效率更高。