DNA-guided CRISPR–Cas12 for cellular RNA targeting

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Authors: Carlos Orosco, Boyu Huang, Santosh R. Rananaware, August P. Bodin, Ivy Browning, Anne Fang, Michael P. Baugh, I. Lange, Yasmin B. Elhabashy, Mahika Balaraju, Jordan G. Lewis, Nayan H. Shah
+5 more Michael P. Hanna, Sarah J. Flannery, Katelyn S. Meister, Vedant Karalkar, Piyush K. Jain
Cited by: 6
References: 52

Abstract

Here, we present ΨDNA, a DNA-based guide that enables RNA targeting by Cas12 nucleases, overcoming the traditional reliance on RNA-guided systems. We engineer ΨDNA to mimic a CRISPR RNA (crRNA) scaffold in reverse orientation, allowing AsCas12a and Cas12i1 to recognize RNA and trigger strong single-stranded DNA trans-cleavage for sensitive detection of diverse RNA species, including 100% accurate hepatitis C virus RNA detection in clinical samples. ΨDNA also achieves 70-95% multiplex knockdown of endogenous intracellular RNA transcripts through ribosome stalling across multiple human cell lines. Mechanistic studies reveal that activity depends on a stem loop that stabilizes a catalytically competent Cas12-ΨDNA-RNA complex. Lastly, codelivery of crRNA and ΨDNA enables simultaneous DNA editing and RNA knockdown with a single effector and modular fusions of different enzymes to AsCas12a extend ΨDNA to RNase H-mediated RNA degradation and METTL3-based epitranscriptomic editing. Together, ΨDNA guides constitute an adaptable toolkit that extends Cas12 systems beyond genome editing and diagnostics to enable precise, programmable control of cellular transcriptomes and their epitranscriptomic marks.

Fields of Study & Subjects

CRISPR and Genetic Engineering RNA regulation and disease Advanced biosensing and bioanalysis techniques

Publication details

Journal / source
Nature Biotechnology
Publisher
Springer Science and Business Media LLC
Publication date
15 May 2026
Language
EN