首页> 外文OA文献 >Placing the RPL32 Promoter Upstream of a Second Promoter Results in a Strongly Increased Number of Stably Transfected Mammalian Cell Lines That Display High Protein Expression Levels
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Placing the RPL32 Promoter Upstream of a Second Promoter Results in a Strongly Increased Number of Stably Transfected Mammalian Cell Lines That Display High Protein Expression Levels

机译:将RPL32启动子置于第二个启动子的上游会导致稳定转染的哺乳动物细胞系数量显着增加,这些细胞系显示出高蛋白表达水平

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摘要

The use of high stringency selection systems commonly results in a strongly diminished number of stably transfected mammalian cell lines. Here we placed twelve different promoters upstream of an adjacent primary promoter and tested whether this might result in an increased number of colonies; this is in the context of a stringent selection system. We found that only the promoter of the human ribosomal protein, RPL32, induced a high number of colonies in CHO-DG44 cells. This phenomenon was observed when the RPL32 promoter was combined with the CMV, SV40, EF1-α, and the β-actin promoters. In addition, these colonies displayed high protein expression levels. The RPL32 promoter had to be functionally intact, since the deletion of a small region upstream of the transcription start site demolished its positive action. We conclude that adding the RPL32 promoter to an expression cassette in cis may be a powerful tool to augment gene expression levels.
机译:高严格性选择系统的使用通常导致稳定转染的哺乳动物细胞系的数量大大减少。在这里,我们在相邻的一级启动子的上游放置了十二个不同的启动子,并测试了这是否会导致菌落数量的增加。这是在严格的选拔制度中。我们发现,只有人类核糖体蛋白RPL32的启动子才能在CHO-DG44细胞中诱导大量菌落。当RPL32启动子与CMV,SV40,EF1-α和β-肌动蛋白启动子结合时,观察到此现象。另外,这些菌落显示出高蛋白表达水平。 RPL32启动子必须是功能完整的,因为转录起始位点上游小区域的缺失会破坏其积极作用。我们得出结论,将RPL32启动子添加至顺式表达盒可能是增强基因表达水平的有力工具。

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