Wiznerowicz Maciej, Trono Didier
Department of Genetics and Microbiology, CMU, Faculty of Medicine, University of Geneva, 1211 Geneva 4, Switzerland.
J Virol. 2003 Aug;77(16):8957-61. doi: 10.1128/jvi.77.16.8957-8951.2003.
RNA interference has emerged as a powerful technique to downregulate the expression of specific genes in cells and in animals, thus opening new perspectives in fields ranging from developmental genetics to molecular therapeutics. Here, we describe a method that significantly expands the potential of RNA interference by permitting the conditional suppression of genes in mammalian cells. Within a lentivirus vector background, we subjected the polymerase III promoter-dependent production of small interfering RNAs to doxycycline-controllable transcriptional repression. The resulting system can achieve the highly efficient and completely drug-inducible knockdown of cellular genes. As lentivirus vectors can stably transduce a wide variety of targets both in vitro and in vivo and can be used to generate transgenic animals, the present system should have broad applications.
RNA干扰已成为一种强大的技术,可下调细胞和动物中特定基因的表达,从而在从发育遗传学到分子治疗学等诸多领域开辟了新的前景。在此,我们描述了一种方法,该方法通过允许在哺乳动物细胞中条件性抑制基因,显著扩展了RNA干扰的潜力。在慢病毒载体背景下,我们使依赖于聚合酶III启动子的小干扰RNA的产生受到强力霉素可控的转录抑制。由此产生的系统能够实现细胞基因的高效且完全药物诱导的敲低。由于慢病毒载体能够在体外和体内稳定转导多种靶标,并且可用于生成转基因动物,因此本系统应具有广泛的应用。