Sumimoto Hidetoshi, Kawakami Yutaka
Division of Cellular Signaling, Institute for Advanced Medical Research, Keio University School of Medicine, Tokyo, Japan.
Methods Mol Biol. 2010;614:187-99. doi: 10.1007/978-1-60761-533-0_13.
Since the discovery of RNA interference (RNAi) in Caenorhabditis elegans in 1998, this mechanism has been found to be conserved in a wide variety of species, including insects, plants, and mammals. In mammals, small (or short) interfering RNA (siRNA) or short hairpin RNA (shRNA) can be expressed by using several expression vectors including lentiviral vectors. The lentiviral vector has several useful characteristics for RNAi experiments including broad host tropism and stable gene transduction to both dividing and nondividing cells, which permits stable depletion of target genes. This technology can be useful for several applications, including basic cancer research.
自1998年在秀丽隐杆线虫中发现RNA干扰(RNAi)以来,已发现该机制在包括昆虫、植物和哺乳动物在内的多种物种中保守存在。在哺乳动物中,小(或短)干扰RNA(siRNA)或短发夹RNA(shRNA)可通过使用包括慢病毒载体在内的多种表达载体来表达。慢病毒载体在RNAi实验中具有几个有用的特性,包括广泛的宿主嗜性以及对分裂细胞和非分裂细胞的稳定基因转导,这使得能够稳定地敲低靶基因。该技术可用于多种应用,包括基础癌症研究。