Tsuchida N, Shih M, Gilden R V, Hatanaka M
J Exp Med. 1974 Jul 1;140(1):218-24. doi: 10.1084/jem.140.1.218.
BALB/3T3 cells transformed by the Kirsten sarcoma virus (nonvirus producer BALB/3T3 cells) and mutant cell lines derived therefrom by treatment with bromodeoxyuridine (BrdU) were analyzed for expression of virus-specific RNA using single-stranded DNA transcripts of Rauscher leukemia virus (RLV), a virus activated in one of the cell lines (58-2T), and Ki-SV-specific DNA transcript; the latter transcript after removal of all sequences cross-reactive with RLV RNA. The Rauscher virus DNA detected multiple copies of viral RNA in virus-producing cells ( approximately 2.5 x 10(3)/cell) whether infected with RLV or activated to produce virus with BrdU. Nonproducer (NP) cells and normal BALB cells showed small numbers of RNA genomes (70-250/cell) and only partial saturation of the transcript. The intracellular RNA sedimented at 35S (main peak) with a variable minor peak at 20S with the exception of one mutant cell, M-43-2 (main peak at 26-27S). The 58-2T transcript reacted preferentially in NP cells and their derivatives with biphasic kinetics suggesting the possibility of sequences specific for the original transforming virus. The size of Ki-SV specific sequences were 30S in mutant cells whether or not complete virus was being produced and independent of in vivo transplantability.
对由 Kirsten 肉瘤病毒转化的 BALB/3T3 细胞(非病毒产生性 BALB/3T3 细胞)以及通过用溴脱氧尿苷(BrdU)处理从中衍生出的突变细胞系,使用劳斯氏白血病病毒(RLV,一种在其中一个细胞系(58 - 2T)中被激活的病毒)的单链 DNA 转录本和 Ki - SV 特异性 DNA 转录本分析病毒特异性 RNA 的表达;后者转录本去除了所有与 RLV RNA 交叉反应的序列。劳斯氏病毒 DNA 在产生病毒的细胞中检测到多个病毒 RNA 拷贝(约 2.5×10³/细胞),无论这些细胞是感染了 RLV 还是用 BrdU 激活以产生病毒。非产生细胞(NP)和正常 BALB 细胞显示出少量的 RNA 基因组(70 - 250/细胞),并且转录本仅部分饱和。细胞内 RNA 以 35S(主峰)沉降,在 20S 处有一个可变的小峰,但有一个突变细胞 M - 43 - 2 除外(主峰在 26 - 27S)。58 - 2T 转录本在 NP 细胞及其衍生物中优先以双相动力学反应,这表明存在原始转化病毒特异性序列的可能性。在突变细胞中,无论是否产生完整病毒,Ki - SV 特异性序列的大小均为 30S,且与体内移植能力无关。