Owen D, Diggelmann H
J Virol. 1983 Jan;45(1):148-54. doi: 10.1128/JVI.45.1.148-154.1983.
Mink lung epithelial cells were transfected with two cloned mouse mammary tumor virus (MMTV) DNAs, a 9-kilobase clone derived from an unintegrated exogenous viral genome and a 14-kilobase clone containing an integrated endogenous provirus along with cellular flanking sequences. Mink lung cells were chosen because they do not contain endogenous MMTV sequences. On the basis of our observation that simian virus 40 DNA efficiently transforms these cells, we isolated cell clones containing MMTV DNA by using transformation with simian virus 40 DNA as a selective marker in cotransfection experiments. Levels of the 9-kilobase MMTV mRNA representing the entire viral genome and of the spliced 4.4-kilobase mRNA which codes for the viral envelope proteins were glucocorticoid dependent in transformed cells. Expression of low levels of Pr77gag, the precursor of the group-specific viral core proteins, and of gPr73env, the precursor of the viral envelope proteins, was also hormone dependent. We conclude that these cloned MMTV DNAs contain all the information necessary for the synthesis of normal viral RNAs and proteins. These findings also provide further evidence that the DNA sequences involved in the hormone responsiveness of MMTV expression are contained within the viral genome.
用两种克隆的小鼠乳腺肿瘤病毒(MMTV)DNA转染水貂肺上皮细胞,一种是来自未整合的外源病毒基因组的9千碱基克隆,另一种是包含整合的内源性前病毒以及细胞侧翼序列的14千碱基克隆。选择水貂肺细胞是因为它们不含有内源性MMTV序列。基于我们观察到猿猴病毒40 DNA能有效地转化这些细胞,我们在共转染实验中以猿猴病毒40 DNA转化作为选择标记,分离出含有MMTV DNA的细胞克隆。在转化细胞中,代表整个病毒基因组的9千碱基MMTV mRNA水平以及编码病毒包膜蛋白的4.4千碱基剪接mRNA水平都依赖于糖皮质激素。低水平的Pr77gag(病毒群特异性核心蛋白的前体)和gPr73env(病毒包膜蛋白的前体)的表达也依赖于激素。我们得出结论,这些克隆的MMTV DNA包含合成正常病毒RNA和蛋白质所需的所有信息。这些发现也进一步证明,MMTV表达的激素反应性所涉及的DNA序列包含在病毒基因组内。