Sheay W, Nelson S, Martinez I, Chu T H, Bhatia S, Dornburg R
Dept. of Microbiology, Robert Wood Johnson Medical School, University of Medicine and Dentistry of New Jersey, Piscataway 08854.
Biotechniques. 1993 Nov;15(5):856-62.
A series of universal eukaryotic gene expression vectors was constructed. All vectors contain a viral promoter and enhancer, a polylinker for insertion of the gene of interest and a polyadenylation sequence. To enhance translation, we inserted the tripartite leader sequence of an adenovirus downstream of the promoter. Using the chloramphenicol acetyl transferase (cat) gene as a marker, we show that the strength of various promoters/enhancers in different cell lines differed by two orders of magnitude. The presence of the tripartite leader increased the efficiency of gene expression up to 18-fold. The level of increase is promoter specific and is most likely influenced by additional sequences flanking the tripartite leader sequence.
构建了一系列通用的真核基因表达载体。所有载体都包含一个病毒启动子和增强子、一个用于插入目的基因的多克隆位点以及一个聚腺苷酸化序列。为了增强翻译,我们在启动子下游插入了腺病毒的三联前导序列。以氯霉素乙酰转移酶(cat)基因作为标记,我们发现不同细胞系中各种启动子/增强子的强度相差两个数量级。三联前导序列的存在使基因表达效率提高了18倍。提高的水平具有启动子特异性,很可能受到三联前导序列侧翼其他序列的影响。