Cahill Anne L, Moore Johnnie M, Sabar Fatima I, Harkins Amy B
Department of Neurobiology, Pharmacology and Physiology, The University of Chicago, Chicago, IL 60637, USA.
J Neurosci Methods. 2007 Nov 30;166(2):236-40. doi: 10.1016/j.jneumeth.2007.07.016. Epub 2007 Aug 1.
RNA interference (RNAi) has quickly become a very powerful technique for specifically suppressing or knocking down the expression of any desired gene. Many fields of research, including neuroscience, have benefitted from RNAi methods. It has been well documented that different small interfering RNAs (siRNAs) and small hairpin RNAs (shRNAs) vary greatly in terms of their effectiveness, and much attention has been focused on guidelines and algorithms for the selection of effective siRNAs. However, it has not been widely appreciated that a single shRNA-expressing plasmid can also produce widely varying levels of knockdown in different stably transfected cell lines derived from the same transfection. Here we report that knockdown of three distinct target proteins varies from minimal to almost complete in independent, stably transfected PC12 cell lines. This variability in knockdown among cell lines emphasizes the importance of characterizing a number of cell lines when attempting to establish stable knockdown cell lines, but also offers the possibility of studying the effects of graded levels of protein expression.
RNA干扰(RNAi)已迅速成为一种非常强大的技术,可用于特异性抑制或敲低任何所需基因的表达。包括神经科学在内的许多研究领域都受益于RNAi方法。有充分的文献记载,不同的小干扰RNA(siRNA)和小发夹RNA(shRNA)在有效性方面差异很大,并且人们一直非常关注有效siRNA的选择指南和算法。然而,尚未得到广泛认可的是,单个表达shRNA的质粒在源自同一转染的不同稳定转染细胞系中也能产生差异很大的敲低水平。在此我们报告,在独立的、稳定转染的PC12细胞系中,三种不同靶蛋白的敲低程度从最小到几乎完全不等。细胞系之间这种敲低的变异性强调了在尝试建立稳定的敲低细胞系时对多个细胞系进行表征的重要性,但也提供了研究蛋白质表达分级水平影响的可能性。