2023
DOI: 10.1126/sciadv.adj8277
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CRISPR-based engineering of RNA viruses

Artem Nemudryi,
Anna Nemudraia,
Joseph E. Nichols
et al.

Abstract: 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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Cited by 3 publications
(2 citation statements)
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“…Precise DNA manipulation has been enabled by breaking DNA at sequence-specific locations and repairing the resulting fragments. In a previous study we applied the concept of break-and-repair to engineer viral RNA genomes in vitro ( 37 ). We extend this approach to make RNA deletions in human cells, which is facilitated by the repair of programmable RNA breaks made using type-III CRISPR complexes.…”
Section: Discussionmentioning
confidence: 99%
“…Precise DNA manipulation has been enabled by breaking DNA at sequence-specific locations and repairing the resulting fragments. In a previous study we applied the concept of break-and-repair to engineer viral RNA genomes in vitro ( 37 ). We extend this approach to make RNA deletions in human cells, which is facilitated by the repair of programmable RNA breaks made using type-III CRISPR complexes.…”
Section: Discussionmentioning
confidence: 99%
“…Precise DNA manipulation, in a test tube or in a cell, has been enabled by breaking DNA at sequence-specific locations and repairing the resulting fragments. In a previous study, we applied the same concept of break-and-repair to engineer viral RNA genomes in vitro (24). Here, we extend this approach to make RNA deletions in human cells, which is facilitated by the repair of programmable RNA breaks made using type III CRISPR complexes.…”
Section: Discussionmentioning
confidence: 99%