| Literature DB >> 29325442 |
Felix F Adams1, Thomas Hoffmann2, Johannes Zuber2, Dirk Heckl3, Axel Schambach1,4, Adrian Schwarzer1,5.
Abstract
Short hairpin RNA (shRNA) screens are powerful tools to probe genetic dependencies in loss-of-function studies, such as the identification of therapeutic targets in cancer research. Lentivirally delivered shRNAs embedded in endogenous microRNA contexts (shRNAmiRs) mediate efficient long-term suppression of target genes suitable for numerous experimental contexts and clinical applications. Here, an easy-to-use laboratory protocol is described, covering the design and pooled assembly of focused shRNAmiR libraries into an optimized, Tet-inducible all-in-one lentiviral vector, packaging of viral particles, followed by retrieval and quantification of hairpin sequences after cellular DNA-recovery. Starting from a gene list to the identification of hits, the protocol enables shRNA screens within 6 weeks.Entities:
Keywords: RNAi; conditional RNAi; lentiviral vector; shRNA Library; shRNA screen
Mesh:
Substances:
Year: 2018 PMID: 29325442 DOI: 10.1089/hgtb.2017.182
Source DB: PubMed Journal: Hum Gene Ther Methods ISSN: 1946-6536 Impact factor: 2.396