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Control of gene editing by manipulation of DNA repair mechanisms.

Eric DannerSanum BashirSaniye YumluWolfgang WurstBenedikt WefersRalf Kühn
Published in: Mammalian genome : official journal of the International Mammalian Genome Society (2017)
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.
Keyphrases
  • genome editing
  • crispr cas
  • dna repair
  • cell cycle
  • dna damage
  • cell proliferation
  • dna damage response
  • nucleic acid
  • single molecule
  • cell free