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Chromosome territory reorganization through artificial chromosome fusion is compatible with cell fate determination and mouse development
Chromosomes occupy discrete spaces in the interphase cell nucleus, called chromosome territory. The structural and functional relevance of chromosome territory remains elusive. We fused chromosome 15 and 17 in mouse haploid embryonic stem cells (haESCs), resulting in distinct changes of territories...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Nature Singapore
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9873915/ https://www.ncbi.nlm.nih.gov/pubmed/36693846 http://dx.doi.org/10.1038/s41421-022-00511-1 |
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author | Wang, Yuang Qu, Zhen Fang, Yi Chen, Yulong Peng, Jiayin Song, Jiawen Li, Jinsong Shi, Jiantao Zhou, Jin-Qiu Zhao, Yun |
author_facet | Wang, Yuang Qu, Zhen Fang, Yi Chen, Yulong Peng, Jiayin Song, Jiawen Li, Jinsong Shi, Jiantao Zhou, Jin-Qiu Zhao, Yun |
author_sort | Wang, Yuang |
collection | PubMed |
description | Chromosomes occupy discrete spaces in the interphase cell nucleus, called chromosome territory. The structural and functional relevance of chromosome territory remains elusive. We fused chromosome 15 and 17 in mouse haploid embryonic stem cells (haESCs), resulting in distinct changes of territories in the cognate chromosomes, but with little effect on gene expression, pluripotency and gamete functions of haESCs. The karyotype-engineered haESCs were successfully implemented in generating heterozygous (2n = 39) and homozygous (2n = 38) mouse models. Mice containing the fusion chromosome are fertile, and their representative tissues and organs display no phenotypic abnormalities, suggesting unscathed development. These results indicate that the mammalian chromosome architectures are highly resilient, and reorganization of chromosome territories can be readily tolerated during cell differentiation and mouse development. |
format | Online Article Text |
id | pubmed-9873915 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Nature Singapore |
record_format | MEDLINE/PubMed |
spelling | pubmed-98739152023-01-26 Chromosome territory reorganization through artificial chromosome fusion is compatible with cell fate determination and mouse development Wang, Yuang Qu, Zhen Fang, Yi Chen, Yulong Peng, Jiayin Song, Jiawen Li, Jinsong Shi, Jiantao Zhou, Jin-Qiu Zhao, Yun Cell Discov Article Chromosomes occupy discrete spaces in the interphase cell nucleus, called chromosome territory. The structural and functional relevance of chromosome territory remains elusive. We fused chromosome 15 and 17 in mouse haploid embryonic stem cells (haESCs), resulting in distinct changes of territories in the cognate chromosomes, but with little effect on gene expression, pluripotency and gamete functions of haESCs. The karyotype-engineered haESCs were successfully implemented in generating heterozygous (2n = 39) and homozygous (2n = 38) mouse models. Mice containing the fusion chromosome are fertile, and their representative tissues and organs display no phenotypic abnormalities, suggesting unscathed development. These results indicate that the mammalian chromosome architectures are highly resilient, and reorganization of chromosome territories can be readily tolerated during cell differentiation and mouse development. Springer Nature Singapore 2023-01-24 /pmc/articles/PMC9873915/ /pubmed/36693846 http://dx.doi.org/10.1038/s41421-022-00511-1 Text en © The Author(s) 2023 https://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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Wang, Yuang Qu, Zhen Fang, Yi Chen, Yulong Peng, Jiayin Song, Jiawen Li, Jinsong Shi, Jiantao Zhou, Jin-Qiu Zhao, Yun Chromosome territory reorganization through artificial chromosome fusion is compatible with cell fate determination and mouse development |
title | Chromosome territory reorganization through artificial chromosome fusion is compatible with cell fate determination and mouse development |
title_full | Chromosome territory reorganization through artificial chromosome fusion is compatible with cell fate determination and mouse development |
title_fullStr | Chromosome territory reorganization through artificial chromosome fusion is compatible with cell fate determination and mouse development |
title_full_unstemmed | Chromosome territory reorganization through artificial chromosome fusion is compatible with cell fate determination and mouse development |
title_short | Chromosome territory reorganization through artificial chromosome fusion is compatible with cell fate determination and mouse development |
title_sort | chromosome territory reorganization through artificial chromosome fusion is compatible with cell fate determination and mouse development |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9873915/ https://www.ncbi.nlm.nih.gov/pubmed/36693846 http://dx.doi.org/10.1038/s41421-022-00511-1 |
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