Mangeot Philippe-Emmanuel, Cosset François-Loïc, Colas Pierre, Mikaelian Ivan
Aptanomics and INSERM U412, Ecole Normale Supérieure, 46, allée d'Italie, 69364 Lyon Cedex 07, France.
Nucleic Acids Res. 2004 Jul 12;32(12):e102. doi: 10.1093/nar/gnh105.
Inducible gene expression systems have contributed significantly to the understanding of molecular regulatory networks. Here we describe a simple and powerful RNA interference-based method that can silence the expression of any transgene. We first used an IRES bicistronic lentiviral vector and showed that targeting the second cistron with a specific siRNA resulted in silencing of both transgenes. We then inserted a siRNA minimal target sequence in the 3'-untranslated region (3'-UTR) of a transgene and showed that the cognate siRNA delivered by a lentiviral vector led to the partial silencing of the transgene. The multimerization of this siRNA target sequence led to the highly efficient silencing of four different transgenes. This new method to silence transgene expression is more versatile than existing methods of conditional inactivation of gene expression, such as transcriptional switches or site-specific recombination. It is applicable to a wide variety of models including primary cells, terminally differentiated cells and transgenic animals.
可诱导基因表达系统对理解分子调控网络做出了重大贡献。在此,我们描述了一种基于RNA干扰的简单而强大的方法,该方法可使任何转基因的表达沉默。我们首先使用了一种内部核糖体进入位点(IRES)双顺反子慢病毒载体,并表明用特定的小干扰RNA(siRNA)靶向第二个顺反子会导致两个转基因都沉默。然后,我们在一个转基因的3'非翻译区(3'-UTR)中插入了一个siRNA最小靶序列,并表明由慢病毒载体递送的同源siRNA导致该转基因部分沉默。这种siRNA靶序列的多聚化导致了四种不同转基因的高效沉默。这种使转基因表达沉默的新方法比现有的基因表达条件失活方法(如转录开关或位点特异性重组)更具通用性。它适用于多种模型,包括原代细胞、终末分化细胞和转基因动物。