Berg P E, Yu J K, Popovic Z, Schumperli D, Johansen H, Rosenberg M, Anderson W F
Mol Cell Biol. 1983 Jul;3(7):1246-54. doi: 10.1128/mcb.3.7.1246-1254.1983.
A series of plasmids was constructed to study the effect of two enhancers, the simian virus 40 72-base-pair repeat and the Harvey sarcoma virus 73-base-pair repeat, on the mouse beta maj-globin promoter. These plasmids contain the mouse beta maj-globin promoter linked to the Escherichia coli galK gene, thus allowing galactokinase enzyme activity to be used as a measure of promoter function. In CV-1 (primate) cells, it was found that an enhancer is required for optimal promoter activity and that the simian virus 40 (primate) enhancer increases galactokinase fourfold more than the Harvey sarcoma virus (mouse) enhancer. In L (mouse) cells, however, the Harvey sarcoma virus enhancer is 1.3-fold stronger than the simian virus 40 enhancer. These data support the hypothesis that enhancer activity can be species specific. Furthermore, when both enhancers are present on the same plasmid, their effect is additive on the beta-globin promoter whether the plasmid is in CV-1 cells or L cells.
构建了一系列质粒,以研究两种增强子,即猴病毒40的72碱基对重复序列和哈维肉瘤病毒的73碱基对重复序列,对小鼠β珠蛋白基因主要启动子的影响。这些质粒包含与大肠杆菌半乳糖激酶基因相连的小鼠β珠蛋白基因主要启动子,因此可以将半乳糖激酶的酶活性用作启动子功能的衡量指标。在CV-1(灵长类)细胞中,发现最佳启动子活性需要增强子,并且猴病毒40(灵长类)增强子使半乳糖激酶增加的幅度比哈维肉瘤病毒(小鼠)增强子高四倍。然而,在L(小鼠)细胞中,哈维肉瘤病毒增强子比猴病毒40增强子强1.3倍。这些数据支持增强子活性具有物种特异性这一假说。此外,当两种增强子存在于同一质粒上时,无论该质粒是在CV-1细胞还是L细胞中,它们对β珠蛋白启动子的作用都是相加的。