Deciphering, Communicating, and Engineering the CRISPR PAM

被引:122
作者
Leenay, Ryan T. [1 ]
Beisel, Chase L. [1 ]
机构
[1] North Carolina State Univ, Dept Chem & Biomol Engn, Raleigh, NC 27695 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
Cas9; Cpf1; CRISPR-Cas systems; PFS; rPAM; RNA-GUIDED ENDONUCLEASE; CRYSTAL-STRUCTURE; DNA CLEAVAGE; SURVEILLANCE COMPLEX; SPACER ACQUISITION; STRUCTURAL BASIS; IMMUNE-SYSTEM; CAS9; RECOGNITION; DEFENSE;
D O I
10.1016/j.jmb.2016.11.024
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
Clustered regularly interspaced short palindromic repeat (CRISPR) loci and their flanking CRISPR-associated (cas) genes make up RNA-guided, adaptive immune systems in prokaryotes whose effector proteins have become powerful tools for basic research and biotechnology. While the Cas effector proteins are remarkably diverse, they commonly rely on protospacer-adjacent motifs (PAMs) as the first step in target recognition. PAM sequences are known to vary considerably between systems and have proven to be difficult to predict, spurring the need for new tools to rapidly identify and communicate these sequences. Recent advances have also shown that Cas proteins can be engineered to alter PAM recognition, opening new opportunities to develop CRISPR-based tools with enhanced targeting capabilities. In this review, we discuss the properties of the CRISPR PAM and the emerging tools for determining, visualizing, and engineering PAM recognition. We also propose a standard means of orienting the PAM to simplify how its location and sequence are communicated. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:177 / 191
页数:15
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