Emerman M, Temin H M
Mol Cell Biol. 1986 Mar;6(3):792-800. doi: 10.1128/mcb.6.3.792-800.1986.
Previously, we described a retrovirus vector that contained two genes: a 5' gene under transcriptional control of the viral long terminal repeat and a 3' gene under transcriptional control of the herpes simplex virus thymidine kinase promoter. By using a biological assay, we found that expression of the 5' gene is suppressed when there was selection for the 3' gene and expression of the 3' gene is suppressed when there is selection for the 5' gene (M. Emerman and H. M. Temin, Cell 39:459-467, 1984). In the present study, we replaced the thymidine kinase promoter with stronger promoters, and we measured expression of the genes in the retrovirus vectors by enzyme activity and RNA analysis. We found that all of the vectors displayed gene suppression when analyzed biochemically, although not when analyzed biologically. The suppressed genes produced about 10 to 50% as much product as when they were selected. The amount of suppression depended on whether the suppressed gene was 5' or 3' to the selected gene and from which promoter the suppressed gene was transcribed. The amount of suppression correlated with a decrease in the amount of steady-state RNA transcribed from the suppressed gene's promoter.
先前,我们描述了一种逆转录病毒载体,其包含两个基因:一个5'基因受病毒长末端重复序列的转录控制,一个3'基因受单纯疱疹病毒胸苷激酶启动子的转录控制。通过生物测定,我们发现当选择3'基因时,5'基因的表达受到抑制;而当选择5'基因时,3'基因的表达受到抑制(M. 埃默曼和H. M. 特明,《细胞》39:459 - 467, 1984)。在本研究中,我们用更强的启动子替换了胸苷激酶启动子,并通过酶活性和RNA分析来测量逆转录病毒载体中基因的表达。我们发现,尽管从生物学分析时未出现基因抑制,但所有载体在进行生化分析时均显示出基因抑制。被抑制的基因产生的产物量约为其被选择时的10%至50%。抑制的程度取决于被抑制基因相对于选择基因是在5'端还是3'端,以及被抑制基因是从哪个启动子转录的。抑制的程度与从被抑制基因启动子转录的稳态RNA量的减少相关。