| Literature DB >> 23707624 |
Mei Zeng1, Marissa S Kuzirian, Lamia Harper, Suzanne Paradis, Takuya Nakayama, Nelson C Lau.
Abstract
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.Entities:
Keywords: Gene silencing; RNA interference; shRNA
Mesh:
Substances:
Year: 2013 PMID: 23707624 PMCID: PMC3966114 DOI: 10.1016/j.ymeth.2013.05.007
Source DB: PubMed Journal: Methods ISSN: 1046-2023 Impact factor: 3.608