锌指核酸酶
转录激活物样效应核酸酶
清脆的
基因组编辑
回文
锌指
计算生物学
生物
遗传学
基因
转录因子
作者
Hiroshi Ochiai,Takashi Yamamoto
出处
期刊:Methods in molecular biology
日期:2023-01-01
卷期号:: 1-25
标识
DOI:10.1007/978-1-0716-3016-7_1
摘要
Zinc finger nucleases (ZFNs) are programmable nucleases that have contributed significantly to past genome-editing research. They are now utilized much less owing to the advent of transcription activator-like effector nucleases (TALENs) and the clustered regularly interspaced short palindromic repeats and CRISPR-associated protein system (CRISPR-Cas). These new methods allow for easier generation of reagents that target genomic sequences of interest and are less labor-intensive than ZFNs at targeting desired sequences. However, fundamental ZFN patents have expired, enabling a wide range of their distribution for clinical and industrial applications. This article introduces a ZFN construction protocol that uses bacterial one-hybrid (B1H) selection and single-strand annealing (SSA) assay.
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