Mathey-Prevot B, Shibuya M, Samarut J, Hanafusa H
J Virol. 1984 May;50(2):325-34. doi: 10.1128/JVI.50.2.325-334.1984.
Fifteen revertants were isolated from three independent clones of rat fibroblasts transformed by Fujinami sarcoma virus (FSV). Three revertant clones resulted from the deletion of the one copy of the FSV provirus, and one encoded an enzymatically inactive, transformation-defective protein. The remaining revertant clones were characterized by a transcriptional block of the provirus. Digestion of chromosomal DNA with MspI and HpaII revealed that the FSV provirus was hypermethylated in these revertants, whereas proviral DNA of their spontaneous retransformants was hypomethylated. Furthermore, the revertants had lost DNase I-hypersensitive sites in and around the FSV provirus. The effect of transcriptional regulation of the FSV provirus was further analyzed in clones showing various degrees of phenotypic transformation. We quantitated v-fps mRNA levels in these cells by liquid hybridization and found that increasing levels of viral RNA correlated with a more pronounced transformed phenotype. These results suggest that transcription of FSV proviral DNA is under both viral and cellular control and that transformation by FSV is a function of the dosage of v-fps mRNA.
从被 Fujinami 肉瘤病毒(FSV)转化的大鼠成纤维细胞的三个独立克隆中分离出 15 个回复突变体。三个回复突变体克隆是由于 FSV 前病毒的一个拷贝缺失所致,其中一个编码一种酶活性缺失、无转化能力的蛋白质。其余的回复突变体克隆的特征是前病毒存在转录阻断。用 MspI 和 HpaII 消化染色体 DNA 显示,这些回复突变体中的 FSV 前病毒发生了高甲基化,而它们的自发再转化体的前病毒 DNA 则发生了低甲基化。此外,回复突变体在 FSV 前病毒及其周围失去了 DNase I 超敏位点。在表现出不同程度表型转化的克隆中进一步分析了 FSV 前病毒转录调控的作用。我们通过液相杂交对这些细胞中的 v-fps mRNA 水平进行定量,发现病毒 RNA 水平的升高与更明显的转化表型相关。这些结果表明,FSV 前病毒 DNA 的转录受病毒和细胞的双重控制,并且 FSV 介导的转化是 v-fps mRNA 剂量的函数。