Matsushita Natsuki, Matsushita Sachi, Hirakawa Satoshi, Higashiyama Shigeki
Functional Genomics Core Laboratory, Ehime University Proteo-Medicine Research Center (ProMRes), Ehime, Japan.
Biosci Biotechnol Biochem. 2013;77(4):776-81. doi: 10.1271/bbb.120917. Epub 2013 Apr 7.
RNA interference has been applied to the development of a method of silencing genes of interest. Short hairpin RNA (shRNA) expression vectors are useful in driving gene-silencing. Standard shRNA vectors produce a knockdown phenotype soon after transduction. An alternative strategy for conditional gene knockdown would be useful to investigate gene functions in a time-dependent manner. In this study, we developed an inducible gene knockdown system based on lentivirus-mediated gene transfer. A single lentivirus vector capable of inducible expression of a designed microRNA-based shRNA was generated using a tetracycline-dependent transactivation system. The lentiviral vector facilitated doxycycline-dependent inducible knockdown specific to the target gene. Withdrawal of doxycycline after transient treatment resulted in complete recovery of target gene expressions to normal levels. Thus the single lentiviral vector developed in this study should be a powerful tool for doxycycline-dependent inducible and reversible RNA interference in molecular genetic studies.
RNA干扰已被应用于开发一种沉默感兴趣基因的方法。短发夹RNA(shRNA)表达载体可用于驱动基因沉默。标准的shRNA载体在转导后不久就会产生基因敲低表型。一种用于条件性基因敲低的替代策略对于以时间依赖的方式研究基因功能将是有用的。在本研究中,我们开发了一种基于慢病毒介导的基因转移的诱导性基因敲低系统。使用四环素依赖性反式激活系统产生了一种能够诱导表达设计的基于微小RNA的shRNA的单一慢病毒载体。该慢病毒载体促进了对目标基因的强力霉素依赖性诱导敲低。短暂处理后去除强力霉素导致目标基因表达完全恢复到正常水平。因此,本研究中开发的单一慢病毒载体应该是分子遗传学研究中用于强力霉素依赖性诱导和可逆RNA干扰的有力工具。