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A most formidable arsenal: genetic technologies for building a better mouse
The mouse is one of the most widely used model organisms for genetic study. The tools available to alter the mouse genome have developed over the preceding decades from forward screens to gene targeting in stem cells to the recent influx of CRISPR approaches. In this review, we first consider the hi...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7528699/ https://www.ncbi.nlm.nih.gov/pubmed/33004485 http://dx.doi.org/10.1101/gad.342089.120 |
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author | Clark, James F. Dinsmore, Colin J. Soriano, Philippe |
author_facet | Clark, James F. Dinsmore, Colin J. Soriano, Philippe |
author_sort | Clark, James F. |
collection | PubMed |
description | The mouse is one of the most widely used model organisms for genetic study. The tools available to alter the mouse genome have developed over the preceding decades from forward screens to gene targeting in stem cells to the recent influx of CRISPR approaches. In this review, we first consider the history of mice in genetic study, the development of classic approaches to genome modification, and how such approaches have been used and improved in recent years. We then turn to the recent surge of nuclease-mediated techniques and how they are changing the field of mouse genetics. Finally, we survey common classes of alleles used in mice and discuss how they might be engineered using different methods. |
format | Online Article Text |
id | pubmed-7528699 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-75286992021-04-01 A most formidable arsenal: genetic technologies for building a better mouse Clark, James F. Dinsmore, Colin J. Soriano, Philippe Genes Dev Review The mouse is one of the most widely used model organisms for genetic study. The tools available to alter the mouse genome have developed over the preceding decades from forward screens to gene targeting in stem cells to the recent influx of CRISPR approaches. In this review, we first consider the history of mice in genetic study, the development of classic approaches to genome modification, and how such approaches have been used and improved in recent years. We then turn to the recent surge of nuclease-mediated techniques and how they are changing the field of mouse genetics. Finally, we survey common classes of alleles used in mice and discuss how they might be engineered using different methods. Cold Spring Harbor Laboratory Press 2020-10-01 /pmc/articles/PMC7528699/ /pubmed/33004485 http://dx.doi.org/10.1101/gad.342089.120 Text en © 2020 Clark et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genesdev.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Review Clark, James F. Dinsmore, Colin J. Soriano, Philippe A most formidable arsenal: genetic technologies for building a better mouse |
title | A most formidable arsenal: genetic technologies for building a better mouse |
title_full | A most formidable arsenal: genetic technologies for building a better mouse |
title_fullStr | A most formidable arsenal: genetic technologies for building a better mouse |
title_full_unstemmed | A most formidable arsenal: genetic technologies for building a better mouse |
title_short | A most formidable arsenal: genetic technologies for building a better mouse |
title_sort | most formidable arsenal: genetic technologies for building a better mouse |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7528699/ https://www.ncbi.nlm.nih.gov/pubmed/33004485 http://dx.doi.org/10.1101/gad.342089.120 |
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