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首页> 外文期刊>The Journal of Biochemistry >A lentiviral vector encoding two fluorescent proteins enables imaging of adenoviral infection via adenovirus-encoded miRNAs in single living cells.
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A lentiviral vector encoding two fluorescent proteins enables imaging of adenoviral infection via adenovirus-encoded miRNAs in single living cells.

机译:编码两种荧光蛋白的慢病毒载体可在单个活细胞中通过腺病毒编码的miRNA对腺病毒感染进行成像。

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摘要

MicroRNAs (miRNAs) are non-coding small RNAs that have been found in various kinds of eukaryotes and viruses. Recently, adenovirus non-coding RNAs, VA RNAs, have been reported to generate miRNAs. Here, we developed a lentiviral vector for monitoring adenovirus-derived miRNAs in living cells. By using red and green fluorescent proteins under the control of bi-directional two distinct promoters, adenoviral infection and consequent miRNA expression was successfully visualized and quantified by the reduction in green fluorescence when 3'-untranslated regions were connected to the target sequences of the adenovirus-derived miRNAs. Our functional analysis using a lentiviral vector is a useful method to examine the activity of miRNA in living mammalian cells.
机译:微小RNA(miRNA)是非编码的小RNA,已在各种真核生物和病毒中发现。近来,已报道腺病毒非编码RNA,VA RNA产生miRNA。在这里,我们开发了一种慢病毒载体,用于监测活细胞中腺病毒衍生的miRNA。通过在双向两个不同启动子的控制下使用红色和绿色荧光蛋白,当3'-非翻译区与腺病毒的靶序列连接时,腺病毒感染和随之而来的miRNA表达通过绿色荧光的减少得以成功可视化和量化来源的miRNA。我们使用慢病毒载体进行的功能分析是检查活的哺乳动物细胞中miRNA活性的有用方法。

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