清脆的
基因组编辑
Cas9
同源定向修复
计算生物学
生物
回文
核酸内切酶
核酸酶
基因
遗传学
DNA
引导RNA
基因组
DNA修复
核苷酸切除修复
作者
Varsha Kumari,Priyanka Kumawat,Sharanabasappa B. Yeri,Shyam Singh Rajput
出处
期刊:Agricultural Reviews
[Agricultural Research Communication Center]
日期:2021-10-13
卷期号: (Of)
被引量:2
摘要
Clustered regularly interspaced short palindromic repeats/CRISPR associated nuclease 9 (CRISPR-Cas9) system is a rapid technology for gene editing. CRISPR-Cas9 is an RNA guided gene editing tool where Cas9 acts as endonuclease by cutting the target DNA strand. Double Stranded Breaks (DBS) can be repaired by non-homologous end joining (NHEJ) and homology-directed repair (HDR). The NHEJ employs DNA ligase IV to rejoin the broken ends which cause insertion or deletion mutations, whereas HDR repairs the DSBs based on a homologous complementary template and results in perfect repair of broken ends. CRISPR-Cas9 impart diverse advantageous features in contrast with the conventional methods. In this review article, we have discussed CRISPR-Cas9 based genome editing along with its mechanism of action and role in crop improvement.
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