首页> 外文期刊>Biochemical and Biophysical Research Communications >shRNA driven by Pol II/T7 dual-promoter system effectively induce cell-specific RNA interference in mammalian cells.
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shRNA driven by Pol II/T7 dual-promoter system effectively induce cell-specific RNA interference in mammalian cells.

机译:由Pol II / T7双启动子系统驱动的shRNA可在哺乳动物细胞中有效诱导细胞特异性RNA干扰。

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摘要

Although Pol III promoters synthesize shRNA and elicit RNAi efficiently, however, a major limitation is that they are constitutively expressed in all cell types. To circumvent this problem, in the present study, we described a novel shRNA vector based on Pol II/T7 dual-promoter couple system: the transcription of shRNA under the control of T7 promoter is dependent on the corresponding T7 RNA polymerase driven by Pol II promoter. Our results strongly demonstrated that such a dual-promoter system can efficiently mediate shRNA expression and specifically reduce the exogenous reporter gene expression in mammalian cells. Furthermore, when hepatoma specific AFP promoter was introduced to control T7 RNA polymerase expression, the RNA interference was permitted only in AFP-producing cells. To our knowledge, this is the first evidence that shRNA can be expressed in a cell-specific manner from Pol II/T7 dual-promoter system in mammalian cells.
机译:尽管Pol III启动子可以有效合成shRNA并引发RNAi,但主要的限制是它们在所有细胞类型中均组成性表达。为了解决这个问题,在本研究中,我们描述了一种基于Pol II / T7双启动子偶联系统的新型shRNA载体:在T7​​启动子控制下,shRNA的转录取决于Pol II驱动的相应T7 RNA聚合酶启动子。我们的结果有力地证明了这种双启动子系统可以有效地介导shRNA的表达,并特异性地降低哺乳动物细胞中外源报道基因的表达。此外,当引入肝癌特异性AFP启动子来控制T7 RNA聚合酶表达时,仅在产生AFP的细胞中允许RNA干扰。据我们所知,这是第一个证据表明shRNA可以在哺乳动物细胞中从Pol II / T7双启动子系统以细胞特异性方式表达。

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