| Literature DB >> 29860898 |
Pingjuan Li1,2, Michael P Marino1, Jizhong Zou3, Takele Argaw1, Michael T Morreale1, Brian J Iaffaldano1, Jakob Reiser1.
Abstract
The adeno-associated virus serotype 2 (AAV2) Rep 78 protein, a strand-specific endonuclease (nickase) promotes site-specific integration of transgene sequences bearing homology arms corresponding to the AAVS1 safe harbor locus. To investigate the efficiency and specificity of this approach, plasmid-based donor vectors were tested in concert with nuclease encoding vectors, including an engineered version of the AAV2 Rep 78 protein, an AAVS1-specific zinc finger nuclease (ZFN), and the CRISPR-Cas9 components in HEK 293 cells. The Rep 78 and ZFN-based approaches were also compared in HEK 293 cells and in human induced pluripotent stem cells using integrase deficient lentiviral vectors. The targeting efficiencies involving the Rep 78 protein were similar to those involving the AAVS1-specific ZFN, while the targeting specificity for the Rep 78 protein was lower compared to that of the ZFN. It is anticipated that the Rep 78 nickase-based targeting approach may ultimately contribute to the reduction of risks associated with other genome editing approaches involving DNA double-strand breaks.Entities:
Keywords: AAVS1 locus; DNA nickase; human iPSCs; integrase-defective lentiviral vectors; site-specific integration; site-specific nuclease
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Year: 2018 PMID: 29860898 PMCID: PMC6016731 DOI: 10.1089/hgtb.2018.052
Source DB: PubMed Journal: Hum Gene Ther Methods ISSN: 1946-6536 Impact factor: 2.396