Guide RNA engineering for versatile Cas9 functionality

被引:73
作者
Nowak, Chance M. [1 ,2 ]
Lawson, Seth [1 ]
Zerez, Megan [1 ,2 ]
Bleris, Leonidas [1 ,2 ,3 ]
机构
[1] Univ Texas Dallas, Dept Biol Sci, Richardson, TX 75080 USA
[2] Univ Texas Dallas, Ctr Syst Biol, Richardson, TX 75080 USA
[3] Univ Texas Dallas, Dept Bioengn, Richardson, TX 75080 USA
基金
美国国家科学基金会;
关键词
STAPHYLOCOCCUS-AUREUS CAS9; PROVIDES ACQUIRED-RESISTANCE; LONG NONCODING RNAS; ONE-STEP GENERATION; HUMAN-CELLS; CRISPR RNA; MAMMALIAN-CELLS; IN-VIVO; STREPTOCOCCUS-THERMOPHILUS; NEISSERIA-MENINGITIDIS;
D O I
10.1093/nar/gkw908
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 Clustered Regularly Interspaced Short Palindromic Repeats system allows a single guide RNA (sgRNA) to direct a protein with combined helicase and nuclease activity to the DNA. Streptococcus pyo-genes Cas9 (SpCas9), a CRISPR-associated protein, has revolutionized our ability to probe and edit the human genomein vitro and in vivo. Arguably, the true modularity of the Cas9 platform is conferred through the ease of sgRNA programmability as well as the degree of modifications the sgRNA can tolerate without compromising its association with SpCas9 and function. In this review, we focus on the properties and recent engineering advances of the sgRNA component in Cas9-mediated genome targeting.
引用
收藏
页码:9555 / 9564
页数:10
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