Exploiting CRISPR/Cas systems for biotechnology

被引:45
|
作者
Sampson, Timothy R. [1 ,2 ,3 ]
Weiss, David S. [2 ,3 ,4 ]
机构
[1] Emory Univ, Sch Med, Dept Microbiol & Immunol, Microbiol & Mol Genet Program, Atlanta, GA 30322 USA
[2] Emory Univ, Emory Vaccine Ctr, Atlanta, GA 30322 USA
[3] Emory Univ, Yerkes Natl Primate Res Ctr, Atlanta, GA 30322 USA
[4] Emory Univ, Sch Med, Div Infect Dis, Dept Med, Atlanta, GA 30322 USA
基金
美国国家卫生研究院;
关键词
biotechnology; Cas9; CRISPR; genome editing; RNAi; CAS SYSTEMS; GENE-EXPRESSION; RNA; SPECIFICITY; ACTIVATION; ENDONUCLEASE; EVOLUTION; CLEAVAGE;
D O I
10.1002/bies.201300135
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
The Cas9 endonuclease is the central component of the Type II CRISPR/Cas system, a prokaryotic adaptive restriction system against invading nucleic acids, such as those originating from bacteriophages and plasmids. Recently, this RNA-directed DNA endonuclease has been harnessed to target DNA sequences of interest. Here, we review the development of Cas9 as an important tool to not only edit the genomes of a number of different prokaryotic and eukaryotic species, but also as an efficient system for site-specific transcriptional repression or activation. Additionally, a specific Cas9 protein has been observed to target an RNA substrate, suggesting that Cas9 may have the ability to be programmed to target RNA as well. Cas proteins from other CRISPR/Cas subtypes may also be exploited in this regard. Thus, CRISPR/Cas systems represent an effective and versatile biotechnological tool, which will have significant impact on future advancements in genome engineering.
引用
收藏
页码:34 / 38
页数:5
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