| Literature DB >> 29266098 |
Hiromi Miura1,2, Rolen M Quadros3, Channabasavaiah B Gurumurthy3,4, Masato Ohtsuka1,2,5.
Abstract
CRISPR/Cas9-based genome editing can easily generate knockout mouse models by disrupting the gene sequence, but its efficiency for creating models that require either insertion of exogenous DNA (knock-in) or replacement of genomic segments is very poor. The majority of mouse models used in research involve knock-in (reporters or recombinases) or gene replacement (e.g., conditional knockout alleles containing exons flanked by LoxP sites). A few methods for creating such models have been reported that use double-stranded DNA as donors, but their efficiency is typically 1-10% and therefore not suitable for routine use. We recently demonstrated that long single-stranded DNAs (ssDNAs) serve as very efficient donors, both for insertion and for gene replacement. We call this method efficient additions with ssDNA inserts-CRISPR (Easi-CRISPR) because it is a highly efficient technology (efficiency is typically 30-60% and reaches as high as 100% in some cases). The protocol takes ∼2 months to generate the founder mice.Entities:
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Year: 2017 PMID: 29266098 PMCID: PMC6058056 DOI: 10.1038/nprot.2017.153
Source DB: PubMed Journal: Nat Protoc ISSN: 1750-2799 Impact factor: 13.491