转录激活物样效应核酸酶
基因组编辑
清脆的
生物
Cas9
同源重组
基因组工程
基因敲除
遗传学
基因
基因靶向
计算生物学
作者
Tetsushi Sakuma,Shota Nakade,Yuto Sakane,Kenichi Suzuki,Takashi Yamamoto
出处
期刊:Nature Protocols
[Nature Portfolio]
日期:2015-12-17
卷期号:11 (1): 118-133
被引量:345
标识
DOI:10.1038/nprot.2015.140
摘要
Programmable nucleases enable engineering of the genome by utilizing endogenous DNA double-strand break (DSB) repair pathways. Although homologous recombination (HR)-mediated gene knock-in is well established, it cannot necessarily be applied in every cell type and organism because of variable HR frequencies. We recently reported an alternative method of gene knock-in, named the PITCh (Precise Integration into Target Chromosome) system, assisted by microhomology-mediated end-joining (MMEJ). MMEJ harnesses independent machinery from HR, and it requires an extremely short homologous sequence (5-25 bp) for DSB repair, resulting in precise gene knock-in with a more easily constructed donor vector. Here we describe a streamlined protocol for PITCh knock-in, including the design and construction of the PITCh vectors, and their delivery to either human cell lines by transfection or to frog embryos by microinjection. The construction of the PITCh vectors requires only a few days, and the entire process takes ∼ 1.5 months to establish knocked-in cells or ∼ 1 week from injection to early genotyping in frog embryos.
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