首页> 美国卫生研究院文献>Nucleic Acids Research >Use of the human EF-1alpha promoter for expression can significantly increase success in establishing stable cell lines with consistent expression: a study using the tetracycline-inducible system in human cancer cells.
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Use of the human EF-1alpha promoter for expression can significantly increase success in establishing stable cell lines with consistent expression: a study using the tetracycline-inducible system in human cancer cells.

机译:使用人类EF-1alpha启动子进行表达可显着提高建立具有一致表达的稳定细胞系的成功率:一项在人类癌细胞中使用四环素诱导系统的研究。

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摘要

Establishing cells with an exogenously introduced gene of interest under the inducible control of tetracycline (Tc) initially requires clonal cell lines stably expressing the tetracycline activator (tTA or rtTA). The originally described plasmid vectors expressing tTA/rtTA are driven by the cytomegalovirus (CMV) immediate early (IE) promoter-enhancer, known for its robust activity in a wide spectrum of cell types. While many reports testify to the utility and efficacy of this construct, instances of inexplicable failure to establish cell lines having inducible expression of the cDNA under study are encountered. Spontaneous extinction of CMV promoter activity in cells has been observed in a temporal and cell type-dependent manner. This could be a contributing factor in the failure to establish Tc-responsive cell lines. We here report that a change of the expression cassette to the human elongation factor-1alpha (EF-1alpha) promoter has permitted successful establishment of several inducible cell lines from diverse human tumor tissue origins. We interpret these results to imply that extinction of rtTA (or tTA) expression might be a significant factor in the lack of success in establishing Tc-inducible cell lines. Moreover, the present findings have general relevance to experiments requiring the use of stable cell lines.
机译:在四环素(Tc)的可诱导控制下用外源导入的目标基因建立细胞最初需要稳定表达四环素激活剂(tTA或rtTA)的克隆细胞系。最初描述的表达tTA / rtTA的质粒载体是由巨细胞病毒(CMV)立即早期(IE)启动子增强子驱动的,该启动子增强子以其在多种细胞类型中的强大活性而闻名。尽管许多报告证明了该构建体的实用性和有效性,但遇到无法解释地建立具有可诱导表达的正在研究的cDNA的细胞系的情况。已经以时间和细胞类型依赖性方式观察到细胞中CMV启动子活性的自发灭绝。这可能是未能建立Tc反应性细胞系的一个促成因素。我们在此报告,表达盒对人类伸长因子-1α(EF-1alpha)启动子的改变已允许成功建立来自多种人类肿瘤组织起源的几种诱导细胞系。我们将这些结果解释为暗示rtTA(或tTA)表达的消失可能是建立Tc诱导型细胞系缺乏成功的重要因素。而且,本发现与需要使用稳定细胞系的实验具有普遍的联系。

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