Abudayyeh Omar O, Gootenberg Jonathan S, Konermann Silvana, Joung Julia, Slaymaker Ian M, Cox David B T, Shmakov Sergey, Makarova Kira S, Semenova Ekaterina, Minakhin Leonid, Severinov Konstantin, Regev Aviv, Lander Eric S, Koonin Eugene V, Zhang Feng
Department of Health Sciences and Technology, Massachusetts Institute of Technology, Cambridge, MA 02139, USA. Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA. McGovern Institute for Brain Research at MIT, Cambridge, MA 02139, USA. Departments of Brain and Cognitive Science and Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA. McGovern Institute for Brain Research at MIT, Cambridge, MA 02139, USA. Departments of Brain and Cognitive Science and Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139, USA. Department of Systems Biology, Harvard Medical School, Boston, MA 02115, USA.
Science. 2016 Aug 5;353(6299):aaf5573. doi: 10.1126/science.aaf5573. Epub 2016 Jun 2.
The clustered regularly interspaced short palindromic repeat (CRISPR)-CRISPR-associated genes (Cas) adaptive immune system defends microbes against foreign genetic elements via DNA or RNA-DNA interference. We characterize the class 2 type VI CRISPR-Cas effector C2c2 and demonstrate its RNA-guided ribonuclease function. C2c2 from the bacterium Leptotrichia shahii provides interference against RNA phage. In vitro biochemical analysis shows that C2c2 is guided by a single CRISPR RNA and can be programmed to cleave single-stranded RNA targets carrying complementary protospacers. In bacteria, C2c2 can be programmed to knock down specific mRNAs. Cleavage is mediated by catalytic residues in the two conserved Higher Eukaryotes and Prokaryotes Nucleotide-binding (HEPN) domains, mutations of which generate catalytically inactive RNA-binding proteins. These results broaden our understanding of CRISPR-Cas systems and suggest that C2c2 can be used to develop new RNA-targeting tools.
成簇规律间隔短回文重复序列(CRISPR)-CRISPR相关基因(Cas)适应性免疫系统通过DNA或RNA-DNA干扰保护微生物免受外来遗传元件的侵害。我们对2类VI型CRISPR-Cas效应蛋白C2c2进行了表征,并证明了其RNA引导的核糖核酸酶功能。来自纤细穆尔菌的C2c2对RNA噬菌体具有干扰作用。体外生化分析表明,C2c2由单个CRISPR RNA引导,并且可以被编程以切割携带互补原间隔序列的单链RNA靶标。在细菌中,C2c2可以被编程以敲低特定的mRNA。切割由两个保守的高等真核生物和原核生物核苷酸结合(HEPN)结构域中的催化残基介导,其中的突变产生催化无活性的RNA结合蛋白。这些结果拓宽了我们对CRISPR-Cas系统的理解,并表明C2c2可用于开发新的RNA靶向工具。