CRISPR-Cas12a: Functional overview and applications

被引:272
作者
Paul, Bijoya [1 ]
Montoya, Guillermo [1 ]
机构
[1] Univ Copenhagen, Novo Nordisk Fdn, Struct Mol Biol Grp, Fac Hlth & Med Sci,Ctr Prot Res, Blegdamsvej 3-B, DK-2200 Copenhagen, Denmark
关键词
CRISPR-Cas12a; RNA guided endonucleases; crRNA biogenesis; Indiscriminate ssDNAse; Endonuclease recycling; Genome editing; RNA-GUIDED ENDONUCLEASE; R-LOOP COMPLEX; STRUCTURAL BASIS; PROGRAMMABLE NUCLEASES; DNA RECOGNITION; CPF1; INTERROGATION; CRISPR/CAS9; MECHANISM; SEQUENCES;
D O I
10.1016/j.bj.2019.10.005
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
Prokaryotes have developed an adaptive immune system called Clustered regularly interspaced short palindromic repeats (CRISPR) to combat attacks by foreign mobile genetic elements (MGEs) such as plasmids and phages. In the past decade, the widely characterized CRISPR-Cas9 enzyme has been redesigned to trigger a genome editing revolution. Class II type V CRISPR-Cas12a is a new RNA guided endonuclease that has been recently harnessed as an alternative genome editing tool, which is emerging as a powerful molecular scissor to consider in the genome editing application landscape. In this review, we aim to provide a mechanistic insight into the working mechanism of Cas12a, comparing it with Cas9, and eventually provide an overview of its current applications in genome editing and biotechnology applications.
引用
收藏
页码:8 / 17
页数:10
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