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

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 mos...

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Detalles Bibliográficos
Autores principales: Erwood, Steven, Gu, Bin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7073597/
https://www.ncbi.nlm.nih.gov/pubmed/32013077
http://dx.doi.org/10.3390/genes11020140
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author Erwood, Steven
Gu, Bin
author_facet Erwood, Steven
Gu, Bin
author_sort Erwood, Steven
collection PubMed
description 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.
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spelling pubmed-70735972020-03-20 Embryo-Based Large Fragment Knock-in in Mammals: Why, How and What’s Next Erwood, Steven Gu, Bin Genes (Basel) Review 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. MDPI 2020-01-29 /pmc/articles/PMC7073597/ /pubmed/32013077 http://dx.doi.org/10.3390/genes11020140 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Erwood, Steven
Gu, Bin
Embryo-Based Large Fragment Knock-in in Mammals: Why, How and What’s Next
title Embryo-Based Large Fragment Knock-in in Mammals: Why, How and What’s Next
title_full Embryo-Based Large Fragment Knock-in in Mammals: Why, How and What’s Next
title_fullStr Embryo-Based Large Fragment Knock-in in Mammals: Why, How and What’s Next
title_full_unstemmed Embryo-Based Large Fragment Knock-in in Mammals: Why, How and What’s Next
title_short Embryo-Based Large Fragment Knock-in in Mammals: Why, How and What’s Next
title_sort embryo-based large fragment knock-in in mammals: why, how and what’s next
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7073597/
https://www.ncbi.nlm.nih.gov/pubmed/32013077
http://dx.doi.org/10.3390/genes11020140
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