AsCas12a tolerates insertions in target DNA

CRISPR-Cas12a enzymes are RNA-guided nucleases widely used for programmable genome editing and diagnostics. Perfect complementarity between guide RNA and target DNA is essential for efficient binding and cleavage by Cas12a. However, we report that a particular ortholog of Cas12a, Acidaminococcus sp. Cas12a (AsCas12a), shows an unexpected tolerance to noncomplementary insertions at various positions in its DNA target. AsCas12a remains functional despite DNA bubbles or loops in the CRISPR-RNA (crRNA)-target DNA duplex, displaying both cis- and trans-cleavage activities even when the target harbors insertions of lengths 1-20 nucleotides in the crRNA-binding region. This activity is sequence-independent and works for ssDNA and is observed on dsDNA in vitro for specific insertion lengths/positions and DNA topologies but is strongly diminished in cells. Among 12 Cas12a orthologs tested, only AsCas12a exhibits this tolerance, making it a unique member of the Cas12a family. Structural analysis suggests a distinctive α-helix in AsCas12a's WED domain is required for this flexibility. Upon deleting this α-helix, AsCas12a loses its ability to tolerate insertions. This discovery can be utilized to detect single-nucleotide polymorphisms and enable protospacer adjacent motif (PAM)-flexible DNA cleavage with Cas12a. Our findings expand our fundamental understanding of CRISPR-Cas12a systems. In conclusion, we uncover and characterize a unique property of AsCas12a to tolerate insertions in its target.

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Publication Details

Journal
Nucleic Acids Research
Published
2025-08-22
DOI
https://doi.org/10.1093/nar/gkaf887
Citations
1
Primary Topic
RNA Interference and Gene Delivery
Type
article
Field-Weighted Citation Impact
0.81

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article

AsCas12a tolerates insertions in target DNA

Noah R. Rakestraw, Luke Samuel W. Sandoval, Katelyn S. Meister, Brianna L.M. Pizzano et al.
1 citations
Nucleic Acids Research
RNA Interference and Gene Delivery
0.81
article

AsCas12a tolerates insertions in target DNA

Noah R. Rakestraw, Luke Samuel W. Sandoval, Katelyn S. Meister, Brianna L.M. Pizzano, Grace M. Shoemaker, Piyush Jain, Long Thành Nguyễn, Emma K. Vesco, David Aguilar-Recarte, I. Lange, Jordan G. Lewis, August P. Bodin, Vedant Karalkar, Santosh R. Rananaware, Dheeraj Pedada, Sarah J. Flannery, Sydney G Antal, Anne Fang
article en
1 citations

Abstract

CRISPR-Cas12a enzymes are RNA-guided nucleases widely used for programmable genome editing and diagnostics. Perfect complementarity between guide RNA and target DNA is essential for efficient binding and cleavage by Cas12a. However, we report that a particular ortholog of Cas12a, Acidaminococcus sp. Cas12a (AsCas12a), shows an unexpected tolerance to noncomplementary insertions at various positions in its DNA target. AsCas12a remains functional despite DNA bubbles or loops in the CRISPR-RNA (crRNA)-target DNA duplex, displaying both cis- and trans-cleavage activities even when the target harbors insertions of lengths 1-20 nucleotides in the crRNA-binding region. This activity is sequence-independent and works for ssDNA and is observed on dsDNA in vitro for specific insertion lengths/positions and DNA topologies but is strongly diminished in cells. Among 12 Cas12a orthologs tested, only AsCas12a exhibits this tolerance, making it a unique member of the Cas12a family. Structural analysis suggests a distinctive α-helix in AsCas12a's WED domain is required for this flexibility. Upon deleting this α-helix, AsCas12a loses its ability to tolerate insertions. This discovery can be utilized to detect single-nucleotide polymorphisms and enable protospacer adjacent motif (PAM)-flexible DNA cleavage with Cas12a. Our findings expand our fundamental understanding of CRISPR-Cas12a systems. In conclusion, we uncover and characterize a unique property of AsCas12a to tolerate insertions in its target.

Nucleic Acids ResearchVol. 53(17)
University of Central Florida (US), Johns Hopkins University (US), Baylor College of Medicine (US), Princeton University (US), Johns Hopkins Medicine (US), University of Florida Health (US), University of Florida (US), Baylor Genetics (US), Massachusetts Institute of Technology (US)
Exxon Mobil Corporation, National Institutes of Health, National Institute of General Medical Sciences, National Institute of Allergy and Infectious Diseases
Openalex Percentile: Top 23%
RNA Interference and Gene Delivery
0.81
DOIOpen Access PDFOpenAlex
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