Nature Communications · 2018 · 218 citations · 32 references
Life SciencesGeneticsMolecular BiologyDna RepairGenome EditingGenome EngineeringCrispr-based EngineeringCrispr-cas SystemsHomologous RecombinationHomology-directed RepairRecombination ProteinsTherapeutic Genome EditingCrispr-cas9 Genome EditingCrispr-cas9-mediated RepairGenome Editing By Homology-directed RepairHomologous Recombination RepairHomology-directed Repair PathwayPrecise Genome EditingSafe Harbor Locus TargetingTransgenic Cell Lines
In genome editing with CRISPR-Cas9, transgene integration often remains challenging. Here, we present an approach for increasing the efficiency of transgene integration by homology-dependent repair (HDR). CtIP, a key protein in early steps of homologous recombination, is fused to Cas9 and stimulates transgene integration by HDR at the human AAVS1 safe harbor locus. A minimal N-terminal fragment of CtIP, designated HE for HDR enhancer, is sufficient to stimulate HDR and this depends on CDK phosphorylation sites and the multimerization domain essential for CtIP activity in homologous recombination. HDR stimulation by Cas9-HE, however, depends on the guide RNA used, a limitation that may be overcome by testing multiple guides to the locus of interest. The Cas9-HE fusion is simple to use and allows obtaining twofold or more efficient transgene integration than that with Cas9 in several experimental systems, including human cell lines, iPS cells, and rat zygotes.
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