Applications of Anti-CRISPR Proteins in Genome Editing and Biotechnology

被引:5
|
作者
Kraus, Carolyn [1 ]
Sontheimer, Erik J. [1 ,2 ,3 ]
机构
[1] Univ Massachusetts Chan Med Sch, RNA Therapeut Inst, Worcester, MA 01605 USA
[2] Univ Massachusetts Chan Med Sch, Program Mol Med, Worcester, MA 01605 USA
[3] Univ Massachusetts Chan Med Sch, Li Weibo Inst Rare Dis Res, Worcester, MA 01605 USA
关键词
GENE DRIVE; DNA; CAS9; INHIBITION; EXPRESSION; SPECIFICITY; MECHANISMS; NUCLEASES; CLEAVAGE; ACRIIA4;
D O I
10.1016/j.jmb.2023.168120
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
In the ten years since the discovery of the first anti-CRISPR (Acr) proteins, the number of validated Acrs has expanded rapidly, as has our understanding of the diverse mechanisms they employ to suppress nat-ural CRISPR-Cas immunity. Many, though not all, function via direct, specific interaction with Cas protein effectors. The abilities of Acr proteins to modulate the activities and properties of CRISPR-Cas effectors have been exploited for an ever-increasing spectrum of biotechnological uses, most of which involve the establishment of control over genome editing systems. This control can be used to minimize off-target editing, restrict editing based on spatial, temporal, or conditional cues, limit the spread of gene drive sys-tems, and select for genome-edited bacteriophages. Anti-CRISPRs have also been developed to over-come bacterial immunity, facilitate viral vector production, control synthetic gene circuits, and other purposes. The impressive and ever-growing diversity of Acr inhibitory mechanisms will continue to allow the tailored applications of Acrs. (c) 2023 Elsevier Ltd. All rights reserved.
引用
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页数:13
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