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Item Type: | Article |
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Title: | Control of gene editing by manipulation of DNA repair mechanisms |
Creators Name: | Danner, E., Bashir, S., Yumlu, S., Wurst, W., Wefers, B. and Kühn, R. |
Abstract: | DNA double-strand breaks (DSBs) are produced intentionally by RNA-guided nucleases to achieve genome editing through DSB repair. These breaks are repaired by one of two main repair pathways, classic non-homologous end joining (c-NHEJ) and homology-directed repair (HDR), the latter being restricted to the S/G2 phases of the cell cycle and notably less frequent. Precise genome editing applications rely on HDR, with the abundant c-NHEJ formed mutations presenting a barrier to achieving high rates of precise sequence modifications. Here, we give an overview of HDR- and c-NHEJ-mediated DSB repair in gene editing and summarize the current efforts to promote HDR over c-NHEJ. |
Keywords: | Biomarkers, CRISPR-Cas Systems, DNA End-Joining Repair, DNA Repair, Gene Editing, Gene Knock-In Techniques, Gene Knockout Techniques, Genetic Testing, Homologous Recombination, Recombinational DNA Repair, Signal Transduction, Animals |
Source: | Mammalian Genome |
ISSN: | 0938-8990 |
Publisher: | Springer |
Volume: | 28 |
Number: | 7-8 |
Page Range: | 262-274 |
Date: | August 2017 |
Additional Information: | Copyright © 2017 Springer Science+Business Media New York |
Official Publication: | https://doi.org/10.1007/s00335-017-9688-5 |
PubMed: | View item in PubMed |
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