Essential Features and Rational Design of CRISPR RNAs that Function with the Cas RAMP Module Complex to Cleave RNAs

被引:239
作者
Hale, Caryn R. [1 ]
Majumdar, Sonali [1 ]
Elmore, Joshua [1 ]
Pfister, Neil [1 ]
Compton, Mark [3 ]
Olson, Sara [4 ]
Resch, Alissa M. [4 ]
Glover, Claiborne V. C., III [1 ]
Graveley, Brenton R. [4 ]
Terns, Rebecca M. [1 ]
Terns, Michael P. [1 ,2 ]
机构
[1] Univ Georgia, Dept Biochem & Mol Biol, Athens, GA 30602 USA
[2] Univ Georgia, Dept Genet, Athens, GA 30602 USA
[3] Univ Georgia, Dept Poultry Sci, Athens, GA 30602 USA
[4] Univ Connecticut Hlth Ctr, Univ Connecticut Stem Cell Inst, Dept Genet & Dev Biol, Farmington, CT 06030 USA
基金
美国国家卫生研究院;
关键词
IMMUNE-SYSTEM; DYNAMIC PROPERTIES; ANTIVIRAL DEFENSE; SEED SEQUENCE; DNA; PROKARYOTES; INTERFERENCE; RECOGNITION; RESISTANCE; ENDORIBONUCLEASE;
D O I
10.1016/j.molcel.2011.10.023
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
Small RNAs target invaders for silencing in the CRISPR-Cas pathways that protect bacteria and archaea from viruses and plasmids. The CRISPR RNAs (crRNAs) contain sequence elements acquired from invaders that guide CRISPR-associated (Gas) proteins back to the complementary invading DNA or RNA. Here, we have analyzed essential features of the crRNAs associated with the Cas RAMP module (Cmr) effector complex, which cleaves targeted RNAs. We show that Cmr crRNAs contain an 8 nucleotide 5' sequence tag (also found on crRNAs associated with other CRISPR-Cas pathways) that is critical for crRNA function and can be used to engineer crRNAs that direct cleavage of novel targets. We also present data that indicate that the Cmr complex cleaves an endogenous complementary RNA in Pyrococcus furiosus, providing direct in vivo evidence of RNA targeting by the CRISPR-Cas system. Our findings indicate that the CRISPR RNA-Cmr protein pathway may be exploited to cleave RNAs of interest.
引用
收藏
页码:292 / 302
页数:11
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