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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
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.
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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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