Lovett M, Clayton C E, Murphy D, Rigby P W, Smith A E, Chaudry F
J Virol. 1982 Dec;44(3):963-73. doi: 10.1128/JVI.44.3.963-973.1982.
Mouse cells transformed by simian virus 40 often contain virus-coded tumor antigens distinct from those synthesized in productively infected permissive cells. The SV3T3 C120 cell line produces no large T-antigen of apparent molecular weight 94,000 but instead a super T-antigen of apparent molecular weight 145,000. We used recombinant DNA techniques to isolate the template for this super T-antigen and determined its structure by DNA sequencing. The integrated viral early transcription unit contains an in-phase, perfect tandem duplication of 1,212 base pairs. Transfer hybridization and endonuclease S1 mapping experiments were performed to elucidate the structures of the stable, cytoplasmic mRNAs of SV3T3 C120 cells, mRNAs of 3.9 and 3.6 kilobases, containing the small t- and large T-antigen splices, respectively, were transcribed from the internally duplicated early transcription unit. We showed by in vitro translation that these mRNAs encode small t-antigen and the super T-antigen of molecular weight 145,000. Peptide mapping studies of the SV3T3 C120 super T-antigen were consistent with its being derived from an internally duplicated template, since the protein has methionine and cysteine tryptic fingerprints virtually identical to those of normal large T-antigen, with certain methionine peptides present in greater than one molar yield.
被猴病毒40转化的小鼠细胞通常含有病毒编码的肿瘤抗原,这些抗原与在产生性感染的允许细胞中合成的抗原有别。SV3T3 C120细胞系不产生表观分子量为94,000的大T抗原,而是产生一种表观分子量为145,000的超级T抗原。我们利用重组DNA技术分离出这种超级T抗原的模板,并通过DNA测序确定了其结构。整合的病毒早期转录单位包含一个1,212个碱基对的同相位、完美串联重复序列。进行了转印杂交和核酸酶S1图谱分析实验,以阐明SV3T3 C120细胞稳定的细胞质mRNA的结构,分别包含小t抗原和大T抗原剪接的3.9和3.6千碱基的mRNA是从内部重复的早期转录单位转录而来的。我们通过体外翻译表明,这些mRNA编码小t抗原和分子量为145,000的超级T抗原。对SV3T3 C120超级T抗原的肽图谱研究与其来源于内部重复模板一致,因为该蛋白质的甲硫氨酸和半胱氨酸胰蛋白酶指纹图谱与正常大T抗原的指纹图谱几乎相同,某些甲硫氨酸肽的摩尔产量大于1。