Advances in engineering CRISPR-Cas9 as a molecular Swiss Army knife

被引:11
|
作者
Meaker, Grace A. [1 ,2 ]
Hair, Emma J. [1 ]
Gorochowski, Thomas E. [1 ,3 ]
机构
[1] Univ Bristol, Sch Biol Sci, Bristol BS8 1TQ, Avon, England
[2] Cardiff Univ, Sch Biosci, Cardiff CF10 3AT, Wales
[3] Univ Bristol, BrisSynBio, Bristol BS8 1TQ, Avon, England
基金
英国生物技术与生命科学研究理事会;
关键词
synthetic biology; CRISPR; genome editing; ethics; Cas9; SEQUENCE-SPECIFIC CONTROL; RNA-GUIDED ENDONUCLEASE; TARGET DNA; CRYSTAL-STRUCTURE; HUMAN-CELLS; HOMOLOGOUS RECOMBINATION; CRISPR/CAS SYSTEM; ESCHERICHIA-COLI; STRUCTURAL BASIS; CAS9; VARIANTS;
D O I
10.1093/synbio/ysaa021
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The RNA-guided endonuclease system CRISPR-Cas9 has been extensively modified since its discovery, allowing its capabilities to extend far beyond double-stranded cleavage to high fidelity insertions, deletions and single base edits. Such innovations have been possible due to the modular architecture of CRISPR-Cas9 and the robustness of its component parts to modifications and the fusion of new functional elements. Here, we review the broad toolkit of CRISPR-Cas9-based systems now available for diverse genome-editing tasks. We provide an overview of their core molecular structure and mechanism and distil the design principles used to engineer their diverse functionalities. We end by looking beyond the biochemistry and toward the societal and ethical challenges that these CRISPR-Cas9 systems face if their transformative capabilities are to be deployed in a safe and acceptable manner.
引用
收藏
页数:16
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