Treisman R, Novak U, Favaloro J, Kamen R
Nature. 1981 Aug 13;292(5824):595-600. doi: 10.1038/292595a0.
A modified polyoma virus genome has been constructed which can encode the middle-T protein, but not the large-T or small-T proteins. This was achieved, starting with the full length viral DNA inserted into a plasmid vector, by replacing a small genomic restriction fragment spanning the middle-T intervening sequence with the equivalent fragment from a cloned partial cDNA copy of the middle-T protein mRNA. Transfection of the modified viral DNA into cultured rat cells efficiently induced the formation of transformed cell foci which gave rise to cell lines that grew as tumours after injection into Fisher rats. The only viral early-region antigen synthesized by the cell lines was the middle-T protein. Expression of the middle-t protein is therefore sufficient to establish and maintain a transformed state. The viral mRNA produced by two of the transformed cell lines was structurally indistinguishable from the normal middle-T mRNA found in productively infected cells, suggesting that RNA splicing is not an essential step in the biogenesis of this messenger.
构建了一种修饰的多瘤病毒基因组,它能够编码中T蛋白,但不能编码大T蛋白或小T蛋白。这是通过将插入质粒载体的全长病毒DNA开始,用来自中T蛋白mRNA的克隆部分cDNA拷贝的等效片段替换跨越中T间隔序列的小基因组限制性片段来实现的。将修饰的病毒DNA转染到培养的大鼠细胞中,有效地诱导了转化细胞灶的形成,这些细胞灶产生了在注射到费希尔大鼠后能作为肿瘤生长的细胞系。这些细胞系合成的唯一病毒早期区域抗原是中T蛋白。因此,中t蛋白的表达足以建立和维持转化状态。由两个转化细胞系产生的病毒mRNA在结构上与在有效感染细胞中发现的正常中T mRNA没有区别,这表明RNA剪接不是该信使生物合成中的必要步骤。