Identifying and Visualizing Functional PAM Diversity across CRISPR-Cas Systems

被引:229
|
作者
Leenay, Ryan T. [1 ]
Maksimchuk, Kenneth R. [1 ]
Slotkowski, Rebecca A. [1 ]
Agrawal, Roma N. [1 ]
Gomaa, Ahmed A. [1 ,2 ]
Briner, Alexandra E. [3 ]
Barrangou, Rodolphe [3 ]
Beisel, Chase L. [1 ]
机构
[1] N Carolina State Univ, Dept Chem & Biomol Engn, Raleigh, NC 27695 USA
[2] Cairo Univ, Fac Engn, Dept Chem Engn, Giza 12613, Egypt
[3] N Carolina State Univ, Dept Food Bioproc & Nutr Sci, 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
RNA-GUIDED ENDONUCLEASE; STRUCTURAL BASIS; DNA RECOGNITION; COMPLEX; INTERFERENCE; CLEAVAGE; IMMUNITY; DEGRADATION; RESISTANCE; PROTEINS;
D O I
10.1016/j.molcel.2016.02.031
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
CRISPR-Cas adaptive immune systems in prokaryotes boast a diversity of protein families and mechanisms of action, where most systems rely on protospacer-adjacent motifs (PAMs) for DNA target recognition. Here, we developed an in vivo, positive, and tunable screen termed PAM-SCANR (PAM screen achieved by NOT-gate repression) to elucidate functional PAMs as well as an interactive visualization scheme termed the PAM wheel to convey individual PAM sequences and their activities. PAM-SCANR and the PAM wheel identified known functional PAMs while revealing complex sequence-activity landscapes for the Bacillus halodurans I-C (Cascade), Escherichia coli I-E (Cascade), Streptococcus thermophilus II-A CRISPR1 (Cas9), and Francisella novicida V-A (Cpf1) systems. The PAM wheel was also readily applicable to existing high-throughput screens and garnered insights into SpyCas9 and SauCas9 PAM diversity. These tools offer powerful means of elucidating and visualizing functional PAMs toward accelerating our ability to understand and exploit the multitude of CRISPR-Cas systems in nature.
引用
收藏
页码:137 / 147
页数:11
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