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Immortalization of primary marmoset skin fibroblasts by CRISPR-Cas9-mediated gene targeting
Immortalized cell lines can be used for diverse in vitro experiments, providing invaluable data before conducting in vivo studies Callithrix jacchus, the common marmoset, is a non-human primate model utilized for studying various human diseases. However, only a few immortalized marmoset cell lines a...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9809370/ https://www.ncbi.nlm.nih.gov/pubmed/36605591 http://dx.doi.org/10.1080/19768354.2022.2151509 |
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author | Jeong, Yeon-Ju Cho, Jeongin Kwak, Jina Sung, Young Hoon Kang, Byeong-Cheol |
author_facet | Jeong, Yeon-Ju Cho, Jeongin Kwak, Jina Sung, Young Hoon Kang, Byeong-Cheol |
author_sort | Jeong, Yeon-Ju |
collection | PubMed |
description | Immortalized cell lines can be used for diverse in vitro experiments, providing invaluable data before conducting in vivo studies Callithrix jacchus, the common marmoset, is a non-human primate model utilized for studying various human diseases. However, only a few immortalized marmoset cell lines are currently available. In the present study, we reveal that CRISPR-Cas9-mediated targeting of the p53 gene or CDKN2A locus is an effective means for immortalizing primary marmoset skin fibroblasts. In addition to frameshift mutations that result in premature stop codons, in-frame mutations potentially destroying the DNA-binding motif of p53 are frequently detected in immortalized cells. Like Cdkn2a-deficient mouse cells, CDKN2A-deficient marmoset cells express wild-type p53 proteins normally respond to genotoxic stresses, including adriamycin and etoposide. Taken together, these findings indicate that Cas9- mediated gene targeting of the p53 gene or CDKN2A locus is an effective tool for establishing immortalized marmoset cell lines with defined genetic alterations. |
format | Online Article Text |
id | pubmed-9809370 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-98093702023-01-04 Immortalization of primary marmoset skin fibroblasts by CRISPR-Cas9-mediated gene targeting Jeong, Yeon-Ju Cho, Jeongin Kwak, Jina Sung, Young Hoon Kang, Byeong-Cheol Anim Cells Syst (Seoul) Articles Immortalized cell lines can be used for diverse in vitro experiments, providing invaluable data before conducting in vivo studies Callithrix jacchus, the common marmoset, is a non-human primate model utilized for studying various human diseases. However, only a few immortalized marmoset cell lines are currently available. In the present study, we reveal that CRISPR-Cas9-mediated targeting of the p53 gene or CDKN2A locus is an effective means for immortalizing primary marmoset skin fibroblasts. In addition to frameshift mutations that result in premature stop codons, in-frame mutations potentially destroying the DNA-binding motif of p53 are frequently detected in immortalized cells. Like Cdkn2a-deficient mouse cells, CDKN2A-deficient marmoset cells express wild-type p53 proteins normally respond to genotoxic stresses, including adriamycin and etoposide. Taken together, these findings indicate that Cas9- mediated gene targeting of the p53 gene or CDKN2A locus is an effective tool for establishing immortalized marmoset cell lines with defined genetic alterations. Taylor & Francis 2022-11-30 /pmc/articles/PMC9809370/ /pubmed/36605591 http://dx.doi.org/10.1080/19768354.2022.2151509 Text en © 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Jeong, Yeon-Ju Cho, Jeongin Kwak, Jina Sung, Young Hoon Kang, Byeong-Cheol Immortalization of primary marmoset skin fibroblasts by CRISPR-Cas9-mediated gene targeting |
title | Immortalization of primary marmoset skin fibroblasts by CRISPR-Cas9-mediated gene targeting |
title_full | Immortalization of primary marmoset skin fibroblasts by CRISPR-Cas9-mediated gene targeting |
title_fullStr | Immortalization of primary marmoset skin fibroblasts by CRISPR-Cas9-mediated gene targeting |
title_full_unstemmed | Immortalization of primary marmoset skin fibroblasts by CRISPR-Cas9-mediated gene targeting |
title_short | Immortalization of primary marmoset skin fibroblasts by CRISPR-Cas9-mediated gene targeting |
title_sort | immortalization of primary marmoset skin fibroblasts by crispr-cas9-mediated gene targeting |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9809370/ https://www.ncbi.nlm.nih.gov/pubmed/36605591 http://dx.doi.org/10.1080/19768354.2022.2151509 |
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