Buetti E, Diggelmann H
Cell. 1981 Feb;23(2):335-45. doi: 10.1016/0092-8674(81)90129-x.
We have cloned circular unintegrated mouse mammary tumor virus (MMTV) DNA from infected rat hepatoma cells in bacteriophage lambda. Seven independent clones containing MMTV DNA of homogeneous length of 9 kb (five) or 10 kb (two) were identified. The five 9 kb clones had identical restriction maps consistent with that of 9 kb unintegrated DNA; the other two were aberrant. MMTV DNA inserts were purified, ligated and used for cotransfection of Ltk- cells together with a plasmid containing the thymidine kinase gene of herpes simplex virus. All Tk+ cell clones acquired new MMTV sequences and those transfected with the 9 kb MMTV DNA synthesized normal viral RNA and proteins. Viral gene expression was increased by the addition of dexamethasone.
我们从感染的大鼠肝癌细胞中,在噬菌体λ载体中克隆出了环状未整合的小鼠乳腺肿瘤病毒(MMTV)DNA。鉴定出了七个独立的克隆,其中五个包含长度均一为9 kb的MMTV DNA,另外两个为10 kb。这五个9 kb的克隆具有与9 kb未整合DNA一致的相同限制性图谱;另外两个则异常。纯化、连接MMTV DNA插入片段,并将其与含有单纯疱疹病毒胸苷激酶基因的质粒一起用于共转染Ltk-细胞。所有Tk+细胞克隆都获得了新的MMTV序列,用9 kb MMTV DNA转染的细胞克隆合成了正常的病毒RNA和蛋白质。通过添加地塞米松可增加病毒基因表达。