反式激活crRNA
Cas9
清脆的
基因组编辑
生物
计算生物学
DNA
核酸内切酶
序列母题
遗传学
基因
作者
Tautvydas Karvelis,Giedrius Gasiūnas,Virginijus Šikšnys
出处
期刊:Methods
[Elsevier BV]
日期:2017-03-23
卷期号:121-122: 3-8
被引量:30
标识
DOI:10.1016/j.ymeth.2017.03.006
摘要
Recently the Cas9, an RNA guided DNA endonuclease, emerged as a powerful tool for targeted genome manipulations. Cas9 protein can be reprogrammed to cleave, bind or nick any DNA target by simply changing crRNA sequence, however a short nucleotide sequence, termed PAM, is required to initiate crRNA hybridization to the DNA target. PAM sequence is recognized by Cas9 protein and must be determined experimentally for each Cas9 variant. Exploration of Cas9 orthologs could offer a diversity of PAM sequences and novel biochemical properties that may be beneficial for genome editing applications. Here we briefly review and compare Cas9 PAM identification assays that can be adopted for other PAM-dependent CRISPR-Cas systems.
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