Programmed DNA Destruction By Miniature CRISPR-Cas14 Enzymes | AIChE

Programmed DNA Destruction By Miniature CRISPR-Cas14 Enzymes

Authors 

Burstein, D., Tel Aviv University
Chen, J. S., University of California Berkeley
Paez, D., Universidad de los Andes
Cofsky, J., UC Berkeley
Banfield, J. F., University of California
Doudna, J. A., University of California Berkeley
CRISPR-Cas systems provide microbes with adaptive immunity to infectious nucleic acids and are widely employed as genome editing tools. These tools use RNA-guided Cas proteins whose large size (950 to 1400 amino acids) has been considered essential to their specific DNA- or RNA-targeting activities. Here we present a set of CRISPR-Cas systems from uncultivated archaea that contain Cas14, a family of exceptionally compact RNA- guided nucleases (400 to 700 amino acids). Despite their small size, Cas14 proteins are capable of targeted single-stranded DNA (ssDNA) cleavage without restrictive sequence requirements. Moreover, target recognition by Cas14 triggers nonspecific cutting of ssDNA molecules, an activity that enables high-fidelity single-nucleotide polymorphism genotyping (Cas14-DETECTR). Metagenomic data show that multiple CRISPR-Cas14 systems evolved independently and suggest a potential evolutionary origin of single- effector CRISPR-based adaptive immunity