Very fast CRISPR on demand
Gene Editing
0301 basic medicine
MRE11 Homologue Protein
DNA Repair
Light
Optical Imaging
Histones
03 medical and health sciences
HEK293 Cells
CRISPR-Associated Protein 9
Humans
DNA Breaks, Double-Stranded
CRISPR-Cas Systems
DNA Cleavage
Phosphorylation
Single-Cell Analysis
DOI:
10.1126/science.aay8204
Publication Date:
2020-06-11T23:15:16Z
AUTHORS (8)
ABSTRACT
Very fast CRISPR on demand
Numerous efforts have been made to improve the temporal resolution of CRISPR-Cas9–mediated DNA cleavage to the hour time scale. Liu
et al.
developed a Cas9 system that achieved genome-editing manipulation at the second time scale (see the Perspective by Medhi and Jasin). Part of the guide RNA is chemically caged, allowing the Cas9-guide RNA complex to bind at a specific genomic locus without cleavage until activation by light. This fast CRISPR system achieves genome editing at high temporal resolution, enabling the study of early molecular events of DNA repair processes. This system also has high spatial resolution at short time scales, allowing editing of one genomic allele while leaving the other unperturbed.
Science
, this issue p.
1265
; see also p.
1180
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