Pecceu F, Komly A, Gardes M, Feunteun J
Laboratorie d'Oncologie Moléculaire, Institut Gustave Roussy, Villejuif, France.
Virology. 1987 Oct;160(2):485-8. doi: 10.1016/0042-6822(87)90022-5.
The biological activity carried by the carboxy-terminal domain of SV40 large T antigen has been investigated by isolating mutants deleted for a stretch of six acidic residues which by analogy with polyoma middle T antigen might be essential for the activity of the protein. We have constructed an "in-phase" deletion of 37 residues that includes the complete acid residues cluster. In order to parallel the polyoma hr-t mutants genotype, the deletion was introduced in virus strains either competent or defective for the small t antigen. We conclude from these experiments that the deletion of this unusual sequence does not affect per se any of the known biological properties of the virus.
通过分离缺失一段六个酸性残基的突变体,对SV40大T抗原羧基末端结构域所携带的生物学活性进行了研究,根据与多瘤病毒中T抗原的类比,这段酸性残基可能对该蛋白的活性至关重要。我们构建了一个37个残基的“同相位”缺失,其中包括完整的酸性残基簇。为了与多瘤病毒hr-t突变体的基因型相似,在有或没有小T抗原的病毒株中引入了该缺失。我们从这些实验中得出结论,这段异常序列的缺失本身并不影响病毒任何已知的生物学特性。