| Literature DB >> 28374058 |
Eric Danner1, Sanum Bashir1,2, Saniye Yumlu1,2, Wolfgang Wurst3,4,5,6, Benedikt Wefers3,4, Ralf Kühn7,8.
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: Gene Editing; Homologous Recombination; Homologous Recombination Pathway; Repair Template; U2OS Cell
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Year: 2017 PMID: 28374058 DOI: 10.1007/s00335-017-9688-5
Source DB: PubMed Journal: Mamm Genome ISSN: 0938-8990 Impact factor: 2.957