Embryo-Based Large Fragment Knock-in in Mammals: Why, How and What's Next

Genes (Basel). 2020 Jan 29;11(2):140. doi: 10.3390/genes11020140.

Abstract

Endonuclease-mediated genome editing technologies, most notably CRISPR/Cas9, have revolutionized animal genetics by allowing for precise genome editing directly through embryo manipulations. As endonuclease-mediated model generation became commonplace, large fragment knock-in remained one of the most challenging types of genetic modification. Due to their unique value in biological and biomedical research, however, a diverse range of technological innovations have been developed to achieve efficient large fragment knock-in in mammalian animal model generation, with a particular focus on mice. Here, we first discuss some examples that illustrate the importance of large fragment knock-in animal models and then detail a subset of the recent technological advancements that have allowed for efficient large fragment knock-in. Finally, we envision the future development of even larger fragment knock-ins performed in even larger animal models, the next step in expanding the potential of large fragment knock-in in animal models.

Keywords: CRISPR-Cas9; HDR; embryo; genome editing; large fragment knock-in.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • CRISPR-Cas Systems
  • DNA Repair
  • Embryo, Mammalian*
  • Gene Editing
  • Gene Knock-In Techniques / methods*
  • Mice

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