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Generation and comparison of CRISPR-Cas9 and Cre-mediated genetically engineered mouse models of sarcoma
Genetically engineered mouse models that employ site-specific recombinase technology are important tools for cancer research but can be costly and time-consuming. The CRISPR-Cas9 system has been adapted to generate autochthonous tumours in mice, but how these tumours compare to tumours generated by...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5508130/ https://www.ncbi.nlm.nih.gov/pubmed/28691711 http://dx.doi.org/10.1038/ncomms15999 |
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author | Huang, Jianguo Chen, Mark Whitley, Melodi Javid Kuo, Hsuan-Cheng Xu, Eric S. Walens, Andrea Mowery, Yvonne M. Van Mater, David Eward, William C. Cardona, Diana M. Luo, Lixia Ma, Yan Lopez, Omar M. Nelson, Christopher E. Robinson-Hamm, Jacqueline N. Reddy, Anupama Dave, Sandeep S. Gersbach, Charles A. Dodd, Rebecca D. Kirsch, David G. |
author_facet | Huang, Jianguo Chen, Mark Whitley, Melodi Javid Kuo, Hsuan-Cheng Xu, Eric S. Walens, Andrea Mowery, Yvonne M. Van Mater, David Eward, William C. Cardona, Diana M. Luo, Lixia Ma, Yan Lopez, Omar M. Nelson, Christopher E. Robinson-Hamm, Jacqueline N. Reddy, Anupama Dave, Sandeep S. Gersbach, Charles A. Dodd, Rebecca D. Kirsch, David G. |
author_sort | Huang, Jianguo |
collection | PubMed |
description | Genetically engineered mouse models that employ site-specific recombinase technology are important tools for cancer research but can be costly and time-consuming. The CRISPR-Cas9 system has been adapted to generate autochthonous tumours in mice, but how these tumours compare to tumours generated by conventional recombinase technology remains to be fully explored. Here we use CRISPR-Cas9 to generate multiple subtypes of primary sarcomas efficiently in wild type and genetically engineered mice. These data demonstrate that CRISPR-Cas9 can be used to generate multiple subtypes of soft tissue sarcomas in mice. Primary sarcomas generated with CRISPR-Cas9 and Cre recombinase technology had similar histology, growth kinetics, copy number variation and mutational load as assessed by whole exome sequencing. These results show that sarcomas generated with CRISPR-Cas9 technology are similar to sarcomas generated with conventional modelling techniques and suggest that CRISPR-Cas9 can be used to more rapidly generate genotypically and phenotypically similar cancers. |
format | Online Article Text |
id | pubmed-5508130 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-55081302017-07-17 Generation and comparison of CRISPR-Cas9 and Cre-mediated genetically engineered mouse models of sarcoma Huang, Jianguo Chen, Mark Whitley, Melodi Javid Kuo, Hsuan-Cheng Xu, Eric S. Walens, Andrea Mowery, Yvonne M. Van Mater, David Eward, William C. Cardona, Diana M. Luo, Lixia Ma, Yan Lopez, Omar M. Nelson, Christopher E. Robinson-Hamm, Jacqueline N. Reddy, Anupama Dave, Sandeep S. Gersbach, Charles A. Dodd, Rebecca D. Kirsch, David G. Nat Commun Article Genetically engineered mouse models that employ site-specific recombinase technology are important tools for cancer research but can be costly and time-consuming. The CRISPR-Cas9 system has been adapted to generate autochthonous tumours in mice, but how these tumours compare to tumours generated by conventional recombinase technology remains to be fully explored. Here we use CRISPR-Cas9 to generate multiple subtypes of primary sarcomas efficiently in wild type and genetically engineered mice. These data demonstrate that CRISPR-Cas9 can be used to generate multiple subtypes of soft tissue sarcomas in mice. Primary sarcomas generated with CRISPR-Cas9 and Cre recombinase technology had similar histology, growth kinetics, copy number variation and mutational load as assessed by whole exome sequencing. These results show that sarcomas generated with CRISPR-Cas9 technology are similar to sarcomas generated with conventional modelling techniques and suggest that CRISPR-Cas9 can be used to more rapidly generate genotypically and phenotypically similar cancers. Nature Publishing Group 2017-07-10 /pmc/articles/PMC5508130/ /pubmed/28691711 http://dx.doi.org/10.1038/ncomms15999 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ 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 | Article Huang, Jianguo Chen, Mark Whitley, Melodi Javid Kuo, Hsuan-Cheng Xu, Eric S. Walens, Andrea Mowery, Yvonne M. Van Mater, David Eward, William C. Cardona, Diana M. Luo, Lixia Ma, Yan Lopez, Omar M. Nelson, Christopher E. Robinson-Hamm, Jacqueline N. Reddy, Anupama Dave, Sandeep S. Gersbach, Charles A. Dodd, Rebecca D. Kirsch, David G. Generation and comparison of CRISPR-Cas9 and Cre-mediated genetically engineered mouse models of sarcoma |
title | Generation and comparison of CRISPR-Cas9 and Cre-mediated genetically engineered mouse models of sarcoma |
title_full | Generation and comparison of CRISPR-Cas9 and Cre-mediated genetically engineered mouse models of sarcoma |
title_fullStr | Generation and comparison of CRISPR-Cas9 and Cre-mediated genetically engineered mouse models of sarcoma |
title_full_unstemmed | Generation and comparison of CRISPR-Cas9 and Cre-mediated genetically engineered mouse models of sarcoma |
title_short | Generation and comparison of CRISPR-Cas9 and Cre-mediated genetically engineered mouse models of sarcoma |
title_sort | generation and comparison of crispr-cas9 and cre-mediated genetically engineered mouse models of sarcoma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5508130/ https://www.ncbi.nlm.nih.gov/pubmed/28691711 http://dx.doi.org/10.1038/ncomms15999 |
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