RNA Therapeutics Institute Publications
Title
Partial DNA-guided Cas9 enables genome editing with reduced off-target activity
UMMS Affiliation
Department of Molecular, Cell and Cancer Biology; Program in Molecular Medicine; Department of Biochemistry and Molecular Pharmacology
Publication Date
2018-03-01
Document Type
Article
Disciplines
Biochemistry, Biophysics, and Structural Biology | Cell and Developmental Biology | Genetics and Genomics | Therapeutics
Abstract
CRISPR-Cas9 is a versatile RNA-guided genome editing tool. Here we demonstrate that partial replacement of RNA nucleotides with DNA nucleotides in CRISPR RNA (crRNA) enables efficient gene editing in human cells. This strategy of partial DNA replacement retains on-target activity when used with both crRNA and sgRNA, as well as with multiple guide sequences. Partial DNA replacement also works for crRNA of Cpf1, another CRISPR system. We find that partial DNA replacement in the guide sequence significantly reduces off-target genome editing through focused analysis of off-target cleavage, measurement of mismatch tolerance and genome-wide profiling of off-target sites. Using the structure of the Cas9-sgRNA complex as a guide, the majority of the 3' end of crRNA can be replaced with DNA nucleotide, and the 5 - and 3'-DNA-replaced crRNA enables efficient genome editing. Cas9 guided by a DNA-RNA chimera may provide a generalized strategy to reduce both the cost and the off-target genome editing in human cells.
DOI of Published Version
10.1038/nchembio.2559
Source
Nat Chem Biol. 2018 Mar;14(3):311-316. doi: 10.1038/nchembio.2559. Epub 2018 Jan 29. Link to article on publisher's site
Journal/Book/Conference Title
Nature chemical biology
Related Resources
PubMed ID
29377001
Repository Citation
Yin H, Song C, Suresh S, Kwan S, Wu Q, Walsh S, Ding J, Bogorad RL, Zhu LJ, Wolfe SA, Koteliansky V, Xue W, Langer R, Anderson DG. (2018). Partial DNA-guided Cas9 enables genome editing with reduced off-target activity. RNA Therapeutics Institute Publications. https://doi.org/10.1038/nchembio.2559. Retrieved from https://escholarship.umassmed.edu/rti_pubs/2