Scott M R, Westphal K H, Rigby P W
Cell. 1983 Sep;34(2):557-67. doi: 10.1016/0092-8674(83)90388-4.
We have used molecular hybridization and cDNA cloning techniques to isolate mouse cellular genes activated in SV40-transformed cells and we show that many of the clones belong to one of four sets. We characterize the cytoplasmic transcripts and genomic sequences homologous to two of these sets. The Set 1 transcription unit(s) is activated in all SV40-transformed cell lines analyzed, and experiments with tsA-mutant-transformed lines show that activation appears to require functional large T-antigen. This transcription unit(s) is also activated in mouse fibroblasts transformed by other agents, including retroviruses and chemical carcinogens. Activation of the Set 2 transcription unit(s) is more restricted, being confined to cell lines transformed by SV40 and retroviruses with distinctive biological properties.
我们利用分子杂交和cDNA克隆技术分离在SV40转化细胞中被激活的小鼠细胞基因,并且我们发现许多克隆属于四组中的一组。我们对与其中两组同源的细胞质转录本和基因组序列进行了表征。Set 1转录单位在所有分析的SV40转化细胞系中均被激活,并且用tsA突变体转化细胞系进行的实验表明,激活似乎需要功能性大T抗原。该转录单位在由其他因子转化的小鼠成纤维细胞中也被激活,这些因子包括逆转录病毒和化学致癌物。Set 2转录单位的激活更具局限性,仅限于由具有独特生物学特性的SV40和逆转录病毒转化的细胞系。