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Tissue-specific activation of gene expression by the Synergistic Activation Mediator (SAM) CRISPRa system in mice.

Charleen HuntSuzanne A HartfordDerek WhiteEvangelos PefanisTimothy HannaClarissa HermanJarrell WileyHeather BrownQi SuYurong XinDennis VoroninHien NguyenJudith AltarejosKeith CrosbyJeffery HainesSarah CancelarichMeghan DrummondSven Moller-TankRyan MalpassJacqueline BuckleyMaria Del Pilar Molina-PortelaGustavo DroguettDavid FrendeweyEric ChiaoBrian ZambrowiczGuochun Gong
Published in: Nature communications (2021)
CRISPR-based transcriptional activation is a powerful tool for functional gene interrogation; however, delivery difficulties have limited its applications in vivo. Here, we created a mouse model expressing all components of the CRISPR-Cas9 guide RNA-directed Synergistic Activation Mediator (SAM) from a single transcript that is capable of activating target genes in a tissue-specific manner. We optimized Lipid Nanoparticles and Adeno-Associated Virus guide RNA delivery approaches to achieve expression modulation of one or more genes in vivo. We utilized the SAM mouse model to generate a hypercholesteremia disease state that we could bidirectionally modulate with various guide RNAs. Additionally, we applied SAM to optimize gene expression in a humanized Transthyretin mouse model to recapitulate human expression levels. These results demonstrate that the SAM gene activation platform can facilitate in vivo research and drug discovery.
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