Cargando…
Efficient Single-Nucleotide Microbial Genome Editing Achieved Using CRISPR/Cpf1 with Maximally 3′-End-Truncated crRNAs
[Image: see text] Mismatch tolerance, a cause of the off-target effect, impedes accurate genome editing with the CRISPR/Cas system. Herein, we observed that oligonucleotide-directed single-base substitutions could be rarely introduced in the microbial genome using CRISPR/Cpf1-mediated negative selec...
Autores principales: | Lee, Ho Joung, Kim, Hyun Ju, Park, Young-Jun, Lee, Sang Jun |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9208014/ https://www.ncbi.nlm.nih.gov/pubmed/35584409 http://dx.doi.org/10.1021/acssynbio.2c00054 |
Ejemplares similares
-
Engineering CRISPR-Cpf1 crRNAs and mRNAs to maximize genome editing efficiency
por: Li, Bin, et al.
Publicado: (2017) -
Miniature CRISPR-Cas12f1-Mediated Single-Nucleotide Microbial Genome Editing Using 3′-Truncated sgRNA
por: Lee, Ho Joung, et al.
Publicado: (2023) -
Genetic editing and interrogation with Cpf1 and caged truncated pre-tRNA-like crRNA in mammalian cells
por: Zhang, Xuhua, et al.
Publicado: (2018) -
PrimedSherlock: a tool for rapid design of highly specific CRISPR-Cas12 crRNAs
por: Mann, James G., et al.
Publicado: (2022) -
Targeted large fragment deletion in plants using paired crRNAs with type I CRISPR system
por: Li, Yingnan, et al.
Publicado: (2023)