Bandyopadhyay P K, Temin H M
Mol Cell Biol. 1984 Apr;4(4):749-54. doi: 10.1128/mcb.4.4.749-754.1984.
The chicken thymidine kinase (tk) gene was inserted into spleen necrosis virus. Thymidine kinase activity was expressed even when the promoter and terminator sequences for tk RNA synthesis were retained. When the promoter was present in the same orientation as the promoter in the long terminal repeat of the virus, deletions occurred both in the virus and in the tk gene, and the thymidine kinase-transforming activity of the recovered virus was low. Splicing of apparent intervening sequences in the tk gene was also observed. When the orientation of the tk promoter was opposite to the promoter in the long terminal repeat, virus synthesis was diminished, whereas thymidine kinase activity was expressed at an elevated level compared with virus in which the promoter was in the same orientation. However, when the apparent tk promoter was deleted from virus with the tk gene in the opposite orientation, a high level of virus synthesis was observed, probably as a result of absence of interference of RNA synthesis from converging promoters. The intervening sequences in the virus in which the promoters were in opposite orientation were not spliced.
将鸡胸苷激酶(tk)基因插入脾坏死病毒。即使保留了tk RNA合成的启动子和终止子序列,仍表达出胸苷激酶活性。当启动子与病毒长末端重复序列中的启动子方向相同时,病毒和tk基因中均发生缺失,回收病毒的胸苷激酶转化活性较低。还观察到tk基因中明显间隔序列的剪接。当tk启动子的方向与长末端重复序列中的启动子相反时,病毒合成减少,而与启动子方向相同的病毒相比,胸苷激酶活性以升高的水平表达。然而,当从启动子方向相反的含tk基因的病毒中删除明显的tk启动子时,观察到高水平的病毒合成,这可能是由于不存在来自汇聚启动子的RNA合成干扰的结果。启动子方向相反的病毒中的间隔序列未被剪接。