Department of Biology, Brandeis University, United States; Rosenstiel Basic Medical Science Research Center, United States.
Methods. 2013 Sep 15;63(2):101-9. doi: 10.1016/j.ymeth.2013.05.007. Epub 2013 May 23.
The RNA interference (RNAi) pathway in animal cells can be harnessed to silence gene expression with artificial small interfering RNAs (siRNAs) or transgenes that express small hairpin RNAs (shRNAs). The transgene-expressing shRNA approach has been adapted into large-scale resources for genome-wide loss-of-function screens, whereas focused studies on a narrow set of genes can be achieved by using individual shRNA constructs from these resources. Although current shRNA repositories generally work, they might fail in certain situations and therefore necessitate other alternatives. We detail here a new highly-accessible and rational design of custom shRNAs that utilizes a refined backbone configuration termed the 'organic' shRNA (OshR) platform. The OshR platform is 'organic' because it conforms more naturally to the endogenous vertebrate miRNAs by maintaining specific bulges and incorporating strategic mismatches to insure the desired guide strand is produced while reducing the accumulation of passenger strands that might contribute to off-target effects. We also demonstrate that the reliability of the OshR platform for gene silencing is increased when sequences target the 3' UnTranslated Region (3'UTR) of a gene. We further compare the OshR platform with the current and emerging shRNA designs, and propose that the OshR platform is a novel approach that can allow investigators to generate custom and effective shRNAs for individual gene functional studies.
动物细胞中的 RNA 干扰 (RNAi) 途径可以被利用,通过人工小干扰 RNA (siRNA) 或表达短发夹 RNA (shRNA) 的转基因来沉默基因表达。转基因表达 shRNA 的方法已被改编为大规模的全基因组功能丧失筛选资源,而通过使用这些资源中的单个 shRNA 构建体,可以实现对一组窄基因的集中研究。尽管当前的 shRNA 存储库通常有效,但在某些情况下可能会失败,因此需要其他替代方法。我们在这里详细介绍了一种新的高度可访问的自定义 shRNA 的合理设计,该设计利用了一种称为“有机”shRNA (OshR) 平台的精制骨架构象。OshR 平台是“有机的”,因为它通过保持特定的凸起并引入战略性错配,更自然地符合内源性脊椎动物 miRNA,从而确保产生所需的引导链,同时减少可能导致脱靶效应的过客链的积累。我们还证明,当序列靶向基因的 3'非翻译区 (3'UTR) 时,OshR 平台对基因沉默的可靠性会增加。我们进一步将 OshR 平台与当前和新兴的 shRNA 设计进行比较,并提出 OshR 平台是一种新的方法,可以允许研究人员为单个基因功能研究生成自定义和有效的 shRNA。