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Centromere mechanical maturation during mammalian cell mitosis
During mitosis, tension develops across the centromere as a result of spindle-based forces. Metaphase tension may be critical in preventing mitotic chromosome segregation errors, however, the nature of force transmission at the centromere and the role of centromere mechanics in controlling metaphase...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6465287/ https://www.ncbi.nlm.nih.gov/pubmed/30988289 http://dx.doi.org/10.1038/s41467-019-09578-z |
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author | Harasymiw, Lauren A. Tank, Damien McClellan, Mark Panigrahy, Neha Gardner, Melissa K. |
author_facet | Harasymiw, Lauren A. Tank, Damien McClellan, Mark Panigrahy, Neha Gardner, Melissa K. |
author_sort | Harasymiw, Lauren A. |
collection | PubMed |
description | During mitosis, tension develops across the centromere as a result of spindle-based forces. Metaphase tension may be critical in preventing mitotic chromosome segregation errors, however, the nature of force transmission at the centromere and the role of centromere mechanics in controlling metaphase tension remains unknown. We combined quantitative, biophysical microscopy with computational analysis to elucidate the mechanics of the centromere in unperturbed, mitotic human cells. We discovered that the mechanical stiffness of the human centromere matures during mitotic progression, which leads to amplified centromere tension specifically at metaphase. Centromere mechanical maturation is disrupted across multiple aneuploid cell lines, leading to a weak metaphase tension signal. Further, increasing deficiencies in centromere mechanical maturation are correlated with rising frequencies of lagging, merotelic chromosomes in anaphase, leading to segregation defects at telophase. Thus, we reveal a centromere maturation process that may be critical to the fidelity of chromosome segregation during mitosis. |
format | Online Article Text |
id | pubmed-6465287 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64652872019-04-17 Centromere mechanical maturation during mammalian cell mitosis Harasymiw, Lauren A. Tank, Damien McClellan, Mark Panigrahy, Neha Gardner, Melissa K. Nat Commun Article During mitosis, tension develops across the centromere as a result of spindle-based forces. Metaphase tension may be critical in preventing mitotic chromosome segregation errors, however, the nature of force transmission at the centromere and the role of centromere mechanics in controlling metaphase tension remains unknown. We combined quantitative, biophysical microscopy with computational analysis to elucidate the mechanics of the centromere in unperturbed, mitotic human cells. We discovered that the mechanical stiffness of the human centromere matures during mitotic progression, which leads to amplified centromere tension specifically at metaphase. Centromere mechanical maturation is disrupted across multiple aneuploid cell lines, leading to a weak metaphase tension signal. Further, increasing deficiencies in centromere mechanical maturation are correlated with rising frequencies of lagging, merotelic chromosomes in anaphase, leading to segregation defects at telophase. Thus, we reveal a centromere maturation process that may be critical to the fidelity of chromosome segregation during mitosis. Nature Publishing Group UK 2019-04-15 /pmc/articles/PMC6465287/ /pubmed/30988289 http://dx.doi.org/10.1038/s41467-019-09578-z Text en © The Author(s) 2019 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 Harasymiw, Lauren A. Tank, Damien McClellan, Mark Panigrahy, Neha Gardner, Melissa K. Centromere mechanical maturation during mammalian cell mitosis |
title | Centromere mechanical maturation during mammalian cell mitosis |
title_full | Centromere mechanical maturation during mammalian cell mitosis |
title_fullStr | Centromere mechanical maturation during mammalian cell mitosis |
title_full_unstemmed | Centromere mechanical maturation during mammalian cell mitosis |
title_short | Centromere mechanical maturation during mammalian cell mitosis |
title_sort | centromere mechanical maturation during mammalian cell mitosis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6465287/ https://www.ncbi.nlm.nih.gov/pubmed/30988289 http://dx.doi.org/10.1038/s41467-019-09578-z |
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