TIGR-Tas: A family of modular RNA-guided DNA-targeting systems in prokaryotes and their viruses

Guilhem Faure(Broad Institute), Makoto Saito(Broad Institute), Max E. Wilkinson(Broad Institute), Natalia Quinones‐Olvera(Broad Institute), Peiyu Xu(Broad Institute), Daniel Flam-Shepherd(Broad Institute), Stephanie Kim(Broad Institute), Nishith R. Reddy(Broad Institute), Shiyou Zhu(Broad Institute), Lilia Evgeniou(Broad Institute), Eugene V. Koonin(National Institutes of Health), Rhiannon K. Macrae(Broad Institute), Feng Zhang(Broad Institute)
Science
February 27, 2025
Cited by 38Open Access
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Abstract

RNA-guided systems provide remarkable versatility, enabling diverse biological functions. Through iterative structural and sequence homology-based mining starting with a guide RNA-interaction domain of Cas9, we identified a family of RNA-guided DNA-targeting proteins in phage and parasitic bacteria. Each system consists of a tandem interspaced guide RNA (TIGR) array and a TIGR-associated (Tas) protein containing a nucleolar protein (Nop) domain, sometimes fused to HNH (TasH)- or RuvC (TasR)-nuclease domains. We show that TIGR arrays are processed into 36-nucleotide RNAs (tigRNAs) that direct sequence-specific DNA binding through a tandem-spacer targeting mechanism. TasR can be reprogrammed for precise DNA cleavage, including in human cells. The structure of TasR reveals striking similarities to box C/D small nucleolar ribonucleoproteins and IS110 RNA-guided transposases, providing insights into the evolution of diverse RNA-guided systems.


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