Nilsson S V, Tyndall C, Magnusson G
J Virol. 1983 Apr;46(1):284-7. doi: 10.1128/JVI.46.1.284-287.1983.
Viable polyoma virus mutants were constructed that had small deletions in the early region of the genome. The deletions together removed most of the segment missing from the genome of the nontransforming mutant dl23 (N. Smolar and B. E. Griffin, J. Virol. 38:958-967, 1981). The transformation properties, as measured by colony formation in soft agar, of mutants with overlapping or contiguous deletions showed that part or all of the middle T antigen segment, consisting of the short amino acid sequence Glu4-Tyr-Met-Pro-Met, was essential for the activity of the protein in transformation. However, the segment could be deleted without significant effect on the in vitro protein kinase activity associated with the middle T antigen.
构建了在基因组早期区域有小缺失的活多瘤病毒突变体。这些缺失共同去除了非转化突变体dl23基因组中缺失的大部分片段(N. 斯莫拉尔和B. E. 格里芬,《病毒学杂志》38:958 - 967, 1981)。通过软琼脂中的集落形成来衡量,具有重叠或连续缺失的突变体的转化特性表明,由短氨基酸序列Glu4 - Tyr - Met - Pro - Met组成的中T抗原片段的部分或全部对于该蛋白在转化中的活性至关重要。然而,该片段的缺失对与中T抗原相关的体外蛋白激酶活性没有显著影响。