3rd International Conference on CRISPR Technologies

Programmed DNA Destruction By Miniature CRISPR-Cas14 Enzymes

Authors

David Burstein, Tel Aviv University
Janice S. Chen, University of California Berkeley
David Paez, Universidad de los Andes
Josh Cofsky, UC Berkeley
Jillian F. Banfield, University of California
Jennifer A. Doudna, 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