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Human T-lymphotropie Virus Tax Activates Human Cytomegalovirus Major-Immediate Early Promoter and Improves Production of Recombinant Proteins in HEK293 Cells

机译:人T淋巴细胞营养税可激活人巨细胞病毒主要早期启动子并改善HEK293细胞中重组蛋白的产生

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摘要

The human cytomegalovirus (CMV) major immediate-early (MIE) promoter is widely used in mammalian cells for production of recombinant proteins. It is of great interest to further enhance protein production driven by the CMV promoter. Here, we report that the Tax protein of human T-lymphotropic virus stimulates the transgene expression under the control of CMV MIE promoter in HEK293 cells. At least threefold increases in transient production of recombinant proteins, including luciferase and two biopharmaceutical proteins (erythropoietin and interferon-y), were detected. Furthermore, cyclic adenosine monophosphate (AMP)-response element binding protein 2 (CREB2) was identified as a cellular cofactor, which might be responsible for Tax transactivation of the CMV MIE promoter. Our results not only demonstrate the potential use of this novel expression strategy for improvement of recombinant protein production in HEK293 cells but also provide the molecular mechanism for Tax-mediated activation of CMV MIE promoter.
机译:人巨细胞病毒(CMV)主要早期(MIE)启动子已广泛用于哺乳动物细胞中,以生产重组蛋白。进一步增强由CMV启动子驱动的蛋白质生产引起了极大的兴趣。在这里,我们报告人类T淋巴病毒的Tax蛋白在HEK293细胞的CMV MIE启动子的控制下刺激转基因表达。重组蛋白的瞬时产量至少增加了三倍,包括萤光素酶和两种生物制药蛋白(促红细胞生成素和干扰素-γ)。此外,环状单磷酸腺苷(AMP)反应元件结合蛋白2(CREB2)被确定为细胞辅因子,可能负责CMV MIE启动子的税转激活。我们的结果不仅证明了这种新颖的表达策略在改善HEK293细胞中重组蛋白生产中的潜在用途,而且还提供了Tax介导的CMV MIE启动子激活的分子机制。

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