Manos M M, Gluzman Y
Mol Cell Biol. 1984 Jun;4(6):1125-33. doi: 10.1128/mcb.4.6.1125-1133.1984.
The large T antigen of simian virus 40 (SV40) is a multifunctional protein that is essential in both the virus lytic cycle and the oncogenic transformation of cells by SV40. To investigate the role of the numerous biochemical and physiological activities of T antigen in the lytic and transformation processes, we have studied DNA replication-deficient, transformation-competent large T-antigen mutants. Here we describe the genetic and biochemical analyses of two such mutants, C2/SV40 and C11/SV40. The mutants were isolated by rescuing the integrated SV40 DNA from C2 and C11 cells (CV-1 cell lines transformed with UV-irradiated SV40). The mutant viral early regions were cloned into the plasmid vector pK1 to generate pC2 and pC11. The mutations that are responsible for the deficiency in viral DNA replication were localized by marker rescue. Subsequent DNA sequencing revealed point mutations that predict amino acid substitutions in the carboxyl third of the protein in both mutants. The pC2 mutation predicts the change of Lys----Arg at amino acid 516. pC11 has two mutations, one predicting a change of Pro----Ser at residue 522, and another predicting a Pro----Arg change at amino acid 549. The two C11 mutations were separated from each other to form two distinct viral genomes in pC11A and pC11B. pC2, pC11, pC11A, and pC11B are able to transform both primary and established rodent cell cultures. The C11 and C11A T antigens are defective in ATPase activity, suggesting that wild-type levels of ATPase activity are not necessary for the oncogenic transformation of cells by T antigen.
猴病毒40(SV40)的大T抗原是一种多功能蛋白,在病毒裂解周期以及SV40介导的细胞致癌转化过程中均起着至关重要的作用。为了研究T抗原众多生化和生理活性在裂解及转化过程中的作用,我们对DNA复制缺陷但具有转化能力的大T抗原突变体进行了研究。在此,我们描述了两个此类突变体C2/SV40和C11/SV40的遗传学及生化分析。这些突变体是通过从C2和C11细胞(用紫外线照射的SV40转化的CV-1细胞系)中拯救整合的SV40 DNA而分离得到的。将突变的病毒早期区域克隆到质粒载体pK1中,构建成pC2和pC11。通过标记拯救定位了导致病毒DNA复制缺陷的突变。随后的DNA测序揭示了点突变,这些突变预测了两个突变体中该蛋白羧基端三分之一区域的氨基酸替换。pC2突变预测第516位氨基酸由赖氨酸变为精氨酸。pC11有两个突变,一个预测第522位残基由脯氨酸变为丝氨酸,另一个预测第549位氨基酸由脯氨酸变为精氨酸。在pC11A和pC11B中,C11的两个突变彼此分离,形成了两个不同的病毒基因组。pC2、pC11、pC11A和pC11B均能够转化原代和已建系的啮齿动物细胞培养物。C11和C11A的T抗原在ATP酶活性方面存在缺陷,这表明T抗原介导细胞致癌转化并不需要野生型水平的ATP酶活性。