Advances in CRISPR-Cas systems for RNA targeting, tracking and editing

被引:96
作者
Wang, Fei [1 ,2 ]
Wang, Lianrong [1 ,2 ]
Zou, Xuan [1 ,3 ]
Duan, Suling [1 ]
Li, Zhiqiang [1 ]
Deng, Zixin [1 ]
Luo, Jie [2 ]
Lee, Sang Yup [3 ]
Chen, Shi [1 ,2 ]
机构
[1] Wuhan Univ, Zhongnan Hosp, Brain Ctr,Minist Educ, Sch Pharmaceut Sci,Key Lab Combinatorial Biosynth, Wuhan 430071, Hubei, Peoples R China
[2] Hubei Univ Med, Taihe Hosp, Shiyan 442000, Hubei, Peoples R China
[3] Korea Adv Inst Sci & Technol, BK21 Plus Program, Dept Chem & Biomol Engn, Daejeon 34141, South Korea
基金
中国国家自然科学基金; 新加坡国家研究基金会;
关键词
CRISPR-Cas systems; RNA targeting; RNA tracking; RNA editing; DOUBLE-STRANDED-RNA; LINKED MOLECULAR BEACONS; NUCLEIC-ACID DETECTION; MESSENGER-RNA; GENE-EXPRESSION; CRYSTAL-STRUCTURE; GUIDED ENDONUCLEASE; SPACER ACQUISITION; DNA CLEAVAGE; CMR COMPLEX;
D O I
10.1016/j.biotechadv.2019.03.016
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Clustered regularly interspaced short palindromic repeat (CRISPR)/CRISPR-associated protein (Cas) systems, especially type II (Cas9) systems, have been widely used in gene/genome targeting. Modifications of Cas9 enable these systems to become platforms for precise DNA manipulations. However, the utilization of CRISPR-Cas systems in RNA targeting remains preliminary. The discovery of type VI CRISPR-Cas systems (Cas13) shed light on RNA-guided RNA targeting. Cas13d, the smallest Cas13 protein, with a length of only similar to 930 amino acids, is a promising platform for RNA targeting compatible with viral delivery systems. Much effort has also been made to develop Cas9, Cas13a and Cas13b applications for RNA-guided RNA targeting. The discovery of new RNA targeting CRISPR-Cas systems as well as the development of RNA-targeting platforms with Cas9 and Cas13 will promote RNA-targeting technology substantially. Here, we review new advances in RNA-targeting CRISPR-Cas systems as well as advances in applications of these systems in RNA targeting, tracking and editing. We also compare these Cas protein-based technologies with traditional technologies for RNA targeting, tracking and editing. Finally, we discuss remaining questions and prospects for the future.
引用
收藏
页码:708 / 729
页数:22
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