Rungger D, Türler H
Proc Natl Acad Sci U S A. 1978 Dec;75(12):6073-7. doi: 10.1073/pnas.75.12.6073.
Purified simian virus 40 and polyoma DNAs injected into nuclei of Xenopus oocytes were transcribed and subsequently translated into virus-specific tumor antigens and capsid proteins. Simian virus 40 large and small tumor antigens synthesized in the oocytes were indistinguishable, by gel electrophoresis and [35S]methionine-labeled tryptic peptide mapping, from the corresponding polypeptides synthesized in CV-1 African green monkey cells. The synthesis of large simian virus 40 tumor antigen implies the correct splicing of its mRNA, which is complementary to nonadjacent nucleotide sequences in the early region of the viral genome. Polyoma DNA directed synthesis of two polyoma tumor antigen polypeptides, 57,000 Mr and small tumor antigen, and of the main capsid protein.
注射到非洲爪蟾卵母细胞核中的纯化猴病毒40(Simian virus 40)和多瘤病毒(polyoma)DNA被转录,随后被翻译成病毒特异性肿瘤抗原和衣壳蛋白。通过凝胶电泳和[35S]甲硫氨酸标记的胰蛋白酶肽图谱分析,卵母细胞中合成的猴病毒40大、小肿瘤抗原与在CV-1非洲绿猴细胞中合成的相应多肽没有区别。猴病毒40大肿瘤抗原的合成意味着其mRNA的正确剪接,该mRNA与病毒基因组早期区域中不相邻的核苷酸序列互补。多瘤病毒DNA指导合成了两种多瘤病毒肿瘤抗原多肽,即57,000 Mr的多肽和小肿瘤抗原,以及主要衣壳蛋白。