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RNA-Guided RNA Cleavage by a CRISPR RNA-Cas Protein Complex
Author(s) -
Caryn Hale,
Peng Zhao,
Sara Olson,
Michael O. Duff,
Brenton R. Graveley,
Lance Wells,
Rebecca M. Terns,
Michael P. Terns
Publication year - 2009
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2009.07.040
Subject(s) - crispr , biology , rna , pyrococcus furiosus , cas9 , genetics , trans activating crrna , rna silencing , crispr interference , guide rna , non coding rna , computational biology , gene , effector , long non coding rna , rna interference , microbiology and biotechnology , archaea
Compelling evidence indicates that the CRISPR-Cas system protects prokaryotes from viruses and other potential genome invaders. This adaptive prokaryotic immune system arises from the clustered regularly interspaced short palindromic repeats (CRISPRs) found in prokaryotic genomes, which harbor short invader-derived sequences, and the CRISPR-associated (Cas) protein-coding genes. Here, we have identified a CRISPR-Cas effector complex that is comprised of small invader-targeting RNAs from the CRISPR loci (termed prokaryotic silencing (psi)RNAs) and the RAMP module (or Cmr) Cas proteins. The psiRNA-Cmr protein complexes cleave complementary target RNAs at a fixed distance from the 3' end of the integral psiRNAs. In Pyrococcus furiosus, psiRNAs occur in two size forms that share a common 5' sequence tag but have distinct 3' ends that direct cleavage of a given target RNA at two distinct sites. Our results indicate that prokaryotes possess a unique RNA silencing system that functions by homology-dependent cleavage of invader RNAs.

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