Editor's cut: DNA cleavage by CRISPR RNA-guided nucleases Cas9 and Cas12a

被引:15
|
作者
Swartjes, Thomas [1 ]
Staals, Raymond H. J. [1 ]
van der Oost, John [1 ]
机构
[1] Wageningen Univ & Res, Lab Microbiol, Stippeneng 4, NL-6708 WE Wageningen, Netherlands
基金
荷兰研究理事会; 欧洲研究理事会;
关键词
REAL-TIME OBSERVATION; TARGETED MUTAGENESIS; SPACER ACQUISITION; CRYSTAL-STRUCTURE; STRUCTURAL BASIS; GENOMIC DNA; CPF1; ENDONUCLEASE; COMPLEX; BASE;
D O I
10.1042/BST20190563
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Discovered as an adaptive immune system of prokaryotes, CRISPR-Cas provides many promising applications. DNA-cleaving Cas enzymes like Cas9 and Cas12a, are of great interest for genome editing. The specificity of these DNA nucleases is determined by RNA guides, providing great targeting adaptability. Besides this general method of programmable DNA cleavage, these nucleases have different biochemical characteristics, that can be exploited for different applications. Although Cas nucleases are highly promising, some room for improvement remains. New developments and discoveries like base editing, prime editing, and CRISPR-associated transposons might address some of these challenges.
引用
收藏
页码:207 / 219
页数:13
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