Abstract
Knock-in mice are useful for evaluating endogenous gene expressions and functions in vivo. Instead of the conventional gene-targeting method using embryonic stem cells, an exogenous DNA sequence can be inserted into the target locus in the zygote using genome editing technology. In this chapter, I describe the generation of epitope-tagged mice using engineered endonuclease and single-stranded oligodeoxynucleotide through the mouse zygote as an example of how to generate a knock-in mouse by genome editing.
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Acknowledgment
This work was supported by a Grant in-Aid for Scientific Research [26712025 and 15K14884] from the Japan Society for the Promotion of Science.
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Fujii, W. (2017). Generation of Knock-in Mouse by Genome Editing. In: Hatada, I. (eds) Genome Editing in Animals. Methods in Molecular Biology, vol 1630. Humana Press, New York, NY. https://doi.org/10.1007/978-1-4939-7128-2_8
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DOI: https://doi.org/10.1007/978-1-4939-7128-2_8
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