| Literature DB >> 26422227 |
Bernd Zetsche1, Jonathan S Gootenberg2, Omar O Abudayyeh3, Ian M Slaymaker3, Kira S Makarova4, Patrick Essletzbichler3, Sara E Volz3, Julia Joung3, John van der Oost5, Aviv Regev6, Eugene V Koonin4, Feng Zhang7.
Abstract
The microbial adaptive immune system CRISPR mediates defense against foreign genetic elements through two classes of RNA-guided nuclease effectors. Class 1 effectors utilize multi-protein complexes, whereas class 2 effectors rely on single-component effector proteins such as the well-characterized Cas9. Here, we report characterization of Cpf1, a putative class 2 CRISPR effector. We demonstrate that Cpf1 mediates robust DNA interference with features distinct from Cas9. Cpf1 is a single RNA-guided endonuclease lacking tracrRNA, and it utilizes a T-rich protospacer-adjacent motif. Moreover, Cpf1 cleaves DNA via a staggered DNA double-stranded break. Out of 16 Cpf1-family proteins, we identified two candidate enzymes from Acidaminococcus and Lachnospiraceae, with efficient genome-editing activity in human cells. Identifying this mechanism of interference broadens our understanding of CRISPR-Cas systems and advances their genome editing applications.Entities:
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Year: 2015 PMID: 26422227 PMCID: PMC4638220 DOI: 10.1016/j.cell.2015.09.038
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582