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利用一组诱导型启动子调整淋巴细胞中的转基因表达水平。

Adjusting transgene expression levels in lymphocytes with a set of inducible promoters.

机构信息

Department Biology, Friedrich-Alexander University Erlangen-Nuremberg, Erlangen, Germany.

出版信息

J Gene Med. 2010 Jun;12(6):501-15. doi: 10.1002/jgm.1461.

Abstract

BACKGROUND

Inducible gene expression systems are powerful research tools and could be of clinical value in the future, with lymphocytes being likely prime application targets. However, currently available regulatable promoters exhibit variation in their efficiency in a cell line-dependent-manner and are notorious for basal leakiness or poor inducibility. Data concerning the regulatory properties of different inducible promoters are scarce for lymphocytes. In the present study, we report a comprehensive analysis of how various inducible promoters perform and how their combination with a transsilencer and a reverse transactivator can result in optimally controlled gene expression in T-cells.

METHODS

The performance of the tetracycline-regulated (Tet)-inducible promoters Tet-responsive element (TRE), mouse mammary tumor virus (MMTV)/TRE, TREtight and second generation TRE (SG/TRE) was compared in several B-cell lines and in Jurkat T-cells using transient transfections in combination with Tet-On. To monitor transgene expression in a Jurkat cell line containing a transsilencer and a reverse transactivator, expression cassettes encoding enhanced green fluorescent protein, CD123 or a constitutively active, cytotoxic caspase-3 were flanked with insulators and stably integrated. The performance of TREtight and SG/TRE was furthermore analysed in transiently transfected primary CD4(+) human T-cells.

RESULTS

The promoters exhibit greatly diverging characteristics. MMTV/TRE permits moderate, TRE and TREtight permits intermediate and SG/TRE permits very high expression levels. TRE and SG/TRE are leaky, whereas MMTV/TRE and TREtight provide stringent expression control. Tetracycline derivatives add flexibility to transgene expression by introducing intermediate expression levels.

CONCLUSIONS

The different expression profiles of the promoters increase the flexibility to adjust transgene expression levels. The promoters provide an additional option to optimize system performance for many applications.

摘要

背景

诱导型基因表达系统是强大的研究工具,将来可能具有临床价值,淋巴细胞可能是主要的应用靶标。然而,目前可用的可调节启动子在细胞系依赖性方面表现出效率的变化,并且以基础泄漏或诱导性差而臭名昭著。关于不同诱导型启动子的调节特性的数据对于淋巴细胞来说很少。在本研究中,我们报告了对各种诱导型启动子的性能以及它们与转录沉默子和反向转录激活子结合如何导致 T 细胞中最佳控制基因表达的综合分析。

方法

使用瞬时转染与 Tet-On 相结合,在几种 B 细胞系和 Jurkat T 细胞中比较了四环素调节(Tet)诱导启动子 Tet 反应元件(TRE)、鼠乳腺肿瘤病毒(MMTV)/TRE、TREtight 和第二代 TRE(SG/TRE)的性能。为了监测含有转录沉默子和反向转录激活子的 Jurkat 细胞系中转基因的表达,用增强型绿色荧光蛋白、CD123 或组成型活性、细胞毒性 Caspase-3 的表达盒进行转染编码,并用绝缘子稳定整合。此外,还分析了瞬时转染的原代 CD4(+)人 T 细胞中 TREtight 和 SG/TRE 的性能。

结果

启动子表现出截然不同的特征。MMTV/TRE 允许适度表达,TRE 和 TREtight 允许中等表达,而 SG/TRE 允许非常高的表达水平。TRE 和 SG/TRE 是渗漏的,而 MMTV/TRE 和 TREtight 提供严格的表达控制。四环素衍生物通过引入中间表达水平为转基因表达提供了灵活性。

结论

启动子的不同表达谱增加了调整转基因表达水平的灵活性。这些启动子为许多应用优化系统性能提供了另一种选择。

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