Cargando…
Suppression of unwanted CRISPR-Cas9 editing by co-administration of catalytically inactivating truncated guide RNAs
CRISPR-Cas9 nucleases are powerful genome engineering tools, but unwanted cleavage at off-target and previously edited sites remains a major concern. Numerous strategies to reduce unwanted cleavage have been devised, but all are imperfect. Here, we report that off-target sites can be shielded from t...
Autores principales: | Rose, John C., Popp, Nicholas A., Richardson, Christopher D., Stephany, Jason J., Mathieu, Julie, Wei, Cindy T., Corn, Jacob E., Maly, Dustin J., Fowler, Douglas M. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7264211/ https://www.ncbi.nlm.nih.gov/pubmed/32483117 http://dx.doi.org/10.1038/s41467-020-16542-9 |
Ejemplares similares
-
Rheostatic Control of Cas9-Mediated DNA Double Strand
Break (DSB) Generation and Genome Editing
por: Rose, John C., et al.
Publicado: (2017) -
Rapidly inducible Cas9 and DSB-ddPCR to probe editing kinetics
por: Rose, John C., et al.
Publicado: (2017) -
CRISPR-Cas9 genome editing induces megabase-scale chromosomal truncations
por: Cullot, Grégoire, et al.
Publicado: (2019) -
The origin of unwanted editing byproducts in gene editing: Origin of unwanted editing byproducts in gene editing
por: Yin, Jianhang, et al.
Publicado: (2022) -
Prime editing with genuine Cas9 nickases minimizes unwanted indels
por: Lee, Jaesuk, et al.
Publicado: (2023)