Widespread anti-CRISPR proteins in virulent bacteriophages inhibit a range of Cas9 proteins

被引:118
作者
Hynes, Alexander P. [1 ,2 ]
Rousseau, Genevieve M. [1 ]
Agudelo, Daniel [3 ]
Goulet, Adeline [4 ,5 ]
Amigues, Beatrice [4 ,5 ]
Loehr, Jeremy [3 ]
Romero, Dennis A. [6 ]
Fremaux, Christophe [7 ]
Horvath, Philippe [7 ]
Doyon, Yannick [3 ]
Cambillau, Christian [4 ,5 ]
Moineau, Sylvain [1 ,8 ]
机构
[1] Univ Laval, Dept Biochim Microbiol & Bioinformat, Fac Sci & Genie, Grp Rech Ecol Buccale,Fac Med Dent, Quebec City, PQ G1V 0A6, Canada
[2] McMaster Univ, Fac Hlth Sci, Dept Med, Farncombe Family Digest Hlth Res Inst, Hamilton, ON L8S 4K1, Canada
[3] Univ Laval, CHU Quebec, Res Ctr, Quebec City, PQ G1V 4G2, Canada
[4] Aix Marseille Univ, Architecture & Fonct Macromol Biol, Campus Luminy,Case 932, F-13288 Marseille 9, France
[5] CNRS, Architecture & Fonct Macromol Biol, Campus Luminy,Case 932, F-13288 Marseille 9, France
[6] DuPont Nutr & Hlth, 3329 Agr Dr, Madison, WI 53716 USA
[7] DuPont Nutr & Hlth, BP 10, F-86220 Dange St Romain, France
[8] Univ Laval, Fac Med Dent, Felix dHerelle Reference Ctr Bacterial Viruses, Quebec City, PQ G1V 0A6, Canada
来源
NATURE COMMUNICATIONS | 2018年 / 9卷
基金
加拿大自然科学与工程研究理事会;
关键词
BACTERIAL IMMUNE-SYSTEM; CRYO-EM STRUCTURES; STREPTOCOCCUS-THERMOPHILUS; SURVEILLANCE COMPLEX; VIRAL SUPPRESSORS; GENOME; DNA; MECHANISM; IDENTIFICATION; PROKARYOTES;
D O I
10.1038/s41467-018-05092-w
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
CRISPR-Cas systems are bacterial anti-viral systems, and bacterial viruses (bacteriophages, phages) can carry anti-CRISPR (Acr) proteins to evade that immunity. Acrs can also fine-tune the activity of CRISPR-based genome-editing tools. While Acrs are prevalent in phages capable of lying dormant in a CRISPR-carrying host, their orthologs have been observed only infrequently in virulent phages. Here we identify AcrIIA6, an Acr encoded in 33% of virulent Streptococcus thermophilus phage genomes. The X-ray structure of AcrIIA6 displays some features unique to this Acr family. We compare the activity of AcrIIA6 to those of other Acrs, including AcrIIA5 (also from S. thermophilus phages), and characterize their effectiveness against a range of CRISPR-Cas systems. Finally, we demonstrate that both Acr families from S. thermophilus phages inhibit Cas9-mediated genome editing of human cells.
引用
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页数:10
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