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• W2288685212 abstract "The adeno-associated virus (AAV)-based targeting vector has been one of the tools commonly used for genome modification in human cell lines. It allows for relatively efficient gene targeting associated with 1-4-log higher ratios of homologous-to-random integration of targeting vectors (H/R ratios) than plasmid-based targeting vectors, without actively introducing DNA double-strand breaks. In this study, we sought to improve the efficiency of AAV-mediated gene targeting by introducing a 2A-based promoter-trap system into targeting constructs. We generated three distinct AAV-based targeting vectors carrying 2A for promoter trapping, each targeting a GFP-based reporter module incorporated into the genome, PIGA exon 6 or PIGA intron 5. The absolute gene targeting efficiencies and H/R ratios attained using these vectors were assessed in multiple human cell lines and compared with those attained using targeting vectors carrying internal ribosome entry site (IRES) for promoter trapping. We found that the use of 2A for promoter trapping increased absolute gene targeting efficiencies by 3.4-28-fold and H/R ratios by 2-5-fold compared to values obtained with IRES. In CRISPR-Cas9-assisted gene targeting using plasmid-based targeting vectors, the use of 2A did not enhance the H/R ratios but did upregulate the absolute gene targeting efficiencies compared to the use of IRES." @default.
• W2288685212 created "2016-06-24" @default.
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• W2288685212 date "2015-12-10" @default.
• W2288685212 modified "2023-09-24" @default.
• W2288685212 title "Improved methods of AAV-mediated gene targeting for human cell lines using ribosome-skipping 2A peptide" @default.
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• W2288685212 doi "https://doi.org/10.1093/nar/gkv1338" @default.
• W2288685212 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4824082" @default.
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• W2288685212 hasPublicationYear "2015" @default.
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