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Humanising the mouse genome piece by piece

To better understand human health and disease, researchers create a wide variety of mouse models that carry human DNA. With recent advances in genome engineering, the targeted replacement of mouse genomic regions with orthologous human sequences has become increasingly viable, ranging from finely tu...

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Detalles Bibliográficos
Autores principales: Zhu, Fei, Nair, Remya R., Fisher, Elizabeth M. C., Cunningham, Thomas J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6478830/
https://www.ncbi.nlm.nih.gov/pubmed/31015419
http://dx.doi.org/10.1038/s41467-019-09716-7
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author Zhu, Fei
Nair, Remya R.
Fisher, Elizabeth M. C.
Cunningham, Thomas J.
author_facet Zhu, Fei
Nair, Remya R.
Fisher, Elizabeth M. C.
Cunningham, Thomas J.
author_sort Zhu, Fei
collection PubMed
description To better understand human health and disease, researchers create a wide variety of mouse models that carry human DNA. With recent advances in genome engineering, the targeted replacement of mouse genomic regions with orthologous human sequences has become increasingly viable, ranging from finely tuned humanisation of individual nucleotides and amino acids to the incorporation of many megabases of human DNA. Here, we examine emerging technologies for targeted genomic humanisation, we review the spectrum of existing genomically humanised mouse models and the insights such models have provided, and consider the lessons learned for designing such models in the future.
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spelling pubmed-64788302019-04-25 Humanising the mouse genome piece by piece Zhu, Fei Nair, Remya R. Fisher, Elizabeth M. C. Cunningham, Thomas J. Nat Commun Review Article To better understand human health and disease, researchers create a wide variety of mouse models that carry human DNA. With recent advances in genome engineering, the targeted replacement of mouse genomic regions with orthologous human sequences has become increasingly viable, ranging from finely tuned humanisation of individual nucleotides and amino acids to the incorporation of many megabases of human DNA. Here, we examine emerging technologies for targeted genomic humanisation, we review the spectrum of existing genomically humanised mouse models and the insights such models have provided, and consider the lessons learned for designing such models in the future. Nature Publishing Group UK 2019-04-23 /pmc/articles/PMC6478830/ /pubmed/31015419 http://dx.doi.org/10.1038/s41467-019-09716-7 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Review Article
Zhu, Fei
Nair, Remya R.
Fisher, Elizabeth M. C.
Cunningham, Thomas J.
Humanising the mouse genome piece by piece
title Humanising the mouse genome piece by piece
title_full Humanising the mouse genome piece by piece
title_fullStr Humanising the mouse genome piece by piece
title_full_unstemmed Humanising the mouse genome piece by piece
title_short Humanising the mouse genome piece by piece
title_sort humanising the mouse genome piece by piece
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6478830/
https://www.ncbi.nlm.nih.gov/pubmed/31015419
http://dx.doi.org/10.1038/s41467-019-09716-7
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