Rassoulzadegan M, Perbal B, Cuzin F
J Virol. 1978 Oct;28(1):1-5. doi: 10.1128/JVI.28.1.1-5.1978.
Fisher rat fibroblasts (FR 3T3), transformed with the tsA30 mutant of simian virus 40 and selected by colony formation in soft agar, maintained the transformed phenotype at high temperature, whereas most transformants isolated from foci were found to undergo a phenotypic reversion toward the normal state in their saturation density, ability to grow in soft agar, and rate of 2-deoxyglucose transport. The temperature-independent phenotype observed in agar-selected transformants was not due to a reversion of the viral mutation. These results, similar to those previously obtained with polyoma virus tsa mutants, further suggest that two distinct mechanisms may operate in both cases for maintaining the transformed phenotype. Immunofluorescence studies suggested a different regulation of T antigen synthesis in these two classes of transformants.
用猿猴病毒40的tsA30突变体转化的Fisher大鼠成纤维细胞(FR 3T3),通过在软琼脂中形成集落进行筛选,在高温下维持转化表型,而从病灶中分离出的大多数转化体在其饱和密度、在软琼脂中生长的能力以及2-脱氧葡萄糖转运速率方面表现出向正常状态的表型逆转。在琼脂选择的转化体中观察到的与温度无关的表型并非由于病毒突变的逆转。这些结果与先前用多瘤病毒tsa突变体获得的结果相似,进一步表明在这两种情况下可能有两种不同的机制来维持转化表型。免疫荧光研究表明这两类转化体中T抗原合成的调节不同。