清脆的
Cas9
基因组编辑
引导RNA
同源定向修复
核酸酶
生物
DNA
核糖核酸
非同源性末端接合
计算生物学
基因
遗传学
同源重组
DNA修复
核苷酸切除修复
作者
Meizhen Liu,Liren Wang,Yongmei Li,Xueyun Ma,Honghui Han,Dali Li
出处
期刊:PubMed
[National Institutes of Health]
日期:2023-01-20
卷期号:45 (1): 78-87
被引量:1
标识
DOI:10.16288/j.yczz.22-354
摘要
The RNA-guided CRISPR/Cas9 genomic editing system consists of a single guide RNA (sgRNA) and a Cas9 nuclease. The two components form a complex in cells and target the genomic loci complementary to the sgRNA. The Cas9 nuclease cleaves the target site creating a double stranded DNA break (DSB). In mammalian cells, DSBs are often repaired via error prone non-homologous end joining (NHEJ) or via homology directed repair (HDR) with the presence of donor DNA templates. Micro-injection of the CRISPR/Cas9 system into the rat embryos enables generation of genetically modified rat models. Here, we describe a detailed protocol for creating gene knockout or knockin rat models via the CRISPR/Cas9 technology.
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