A Tale of Two Moieties: Rapidly Evolving CRISPR/Cas-Based Genome Editing

被引:24
|
作者
Yang, Li [1 ,2 ]
Chen, Jia [2 ,3 ]
机构
[1] Univ Chinese Acad Sci, CAS MPG Partner Inst Computat Biol, CAS Key Lab Computat Biol, Shanghai Inst Nutr & Hlth,Chinese Acad Sci, Shanghai 200031, Peoples R China
[2] ShanghaiTech Univ, Sch Life Sci & Technol, Shanghai 201210, Peoples R China
[3] Chinese Acad Sci, CAS Ctr Excellence Mol Cell Sci, Shanghai Inst Biochem & Cell Biol, Shanghai, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
RNA-GUIDED ENDONUCLEASE; URACIL-DNA GLYCOSYLASE; DOUBLE-STRAND BREAKS; OFF-TARGET; CRYSTAL-STRUCTURE; CRISPR-CAS9; NUCLEASES; STRUCTURAL BASIS; GENE-REGULATION; HUMAN CANCERS; HUMAN-CELLS;
D O I
10.1016/j.tibs.2020.06.003
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
Two major moieties in genome editing are required for precise genetic changes: the locator moiety for target binding and the effector moiety for genetic engineering. By taking advantage of CRISPR/Cas, which consists of different modules for indepen- dent target binding and cleavage, a spectrum of precise and versatile genome editing technologies have been developed for broad applications in biomedical re- search, biotechnology, and therapeutics. Here, we briefly summarize the progress of genome editing systems from a view of both locator and effector moieties and highlight the advance of newly reported CRISPR-conjugated base editing and prime editing systems. We also underscore distinct mechanisms of off-target effects in CRISPR-conjugated systems and further discuss possible strategies to reduce off-target mutations in the future.
引用
收藏
页码:874 / 888
页数:15
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