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Targeted Mutagenesis in Mice Using a Base Editor

Authors
Jeong, Tae YeongLim, Soo-YeonSeong, Je KyungKim, Kyoungmi
Issue Date
Jan-2023
Publisher
Humana Press Inc.
Keywords
Adenine base editor; CRISPR system; Cytosine base editor; Mouse model generation; Nucleotide substitution; Targeted mutagenesis
Citation
Methods in molecular biology (Clifton, N.J.), v.2606, pp 99 - 119
Pages
21
Indexed
SCOPUS
Journal Title
Methods in molecular biology (Clifton, N.J.)
Volume
2606
Start Page
99
End Page
119
URI
https://scholarworks.korea.ac.kr/kumedicine/handle/2021.sw.kumedicine/62832
DOI
10.1007/978-1-0716-2879-9_9
ISSN
1064-3745
1940-6029
Abstract
Base editors, such as cytosine and adenine base editors, are composed of nickase Cas9 (nCas9) and deaminase and serve as Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)-based enzymatic tools for specific nucleotide substitutions. They are mainly the most effective genome editing tools for introducing point mutations, such as C-to-T and A-to-G conversions. The enhanced base editor, a C-to-G base editor (CGBE), can perform other nucleotide substitutions, such as C-to-G conversions. Here, we introduce a method for generating mouse models with point mutations using a base editing system. © 2023, The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.
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