CRISPR RNA-guided endonucleases have enabled precise editing of DNA. However, options for editing RNA remain limited. Here, we combine sequence-specific RNA cleavage by CRISPR ribonucleases with programmable RNA repair to make precise deletions and insertions in RNA. This work establishes a recombinant RNA technology with immediate applications for the facile engineering of RNA viruses.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10499312 | PMC |
http://dx.doi.org/10.1126/sciadv.adj8277 | DOI Listing |
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