| Literature DB >> 34432885 |
Masumi Namba1, Tomoe Kobayashi1, Takayuki Koyano1, Mayumi Kohno1, Masato Ohtsuka2,3, Makoto Matsuyama1.
Abstract
Recent advances in the CRISPR/Cas9 system have demonstrated it to be an efficient gene-editing technology for various organisms. Laboratory mice and rats are widely used as common models of human diseases; however, the current standard method to create genome-engineered animals is laborious and involves three major steps: isolation of zygotes from females, ex vivo micromanipulation of zygotes, and implantation into pseudopregnant females. To circumvent this, we recently developed a novel method named Genome-editing via Oviductal Nucleic Acids Delivery (GONAD). This method does not require the ex vivo handling of embryos; instead, it can execute gene editing with just one step, via the delivery of a genome-editing mixture into embryos in the oviduct, by electroporation. Here, we present a further improvement of GONAD that is easily applicable to both mice and rats. It is a rapid, low-cost, and ethical approach fulfilling the 3R principles of animal experimentation: Reduction, Replacement, and Refinement. This method has been reconstructed and renamed as "improved GONAD (i-GONAD)" for mice, and "rat improved GONAD (rGONAD)" for rats.Entities:
Keywords: CRISPR/Cas9; i-GONAD; in vivo electroporation; knock-out; rGONAD
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Year: 2021 PMID: 34432885 DOI: 10.1111/dgd.12746
Source DB: PubMed Journal: Dev Growth Differ ISSN: 0012-1592 Impact factor: 2.053