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NuMA regulates mitotic spindle assembly, structural dynamics and function via phase separation
A functional mitotic spindle is essential for accurate chromosome congression and segregation during cell proliferation; however, the underlying mechanisms of its assembly remain unclear. Here we show that NuMA regulates this assembly process via phase separation regulated by Aurora A. NuMA undergoe...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8660824/ https://www.ncbi.nlm.nih.gov/pubmed/34887424 http://dx.doi.org/10.1038/s41467-021-27528-6 |
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author | Sun, Mengjie Jia, Mingkang Ren, He Yang, Biying Chi, Wangfei Xin, Guangwei Jiang, Qing Zhang, Chuanmao |
author_facet | Sun, Mengjie Jia, Mingkang Ren, He Yang, Biying Chi, Wangfei Xin, Guangwei Jiang, Qing Zhang, Chuanmao |
author_sort | Sun, Mengjie |
collection | PubMed |
description | A functional mitotic spindle is essential for accurate chromosome congression and segregation during cell proliferation; however, the underlying mechanisms of its assembly remain unclear. Here we show that NuMA regulates this assembly process via phase separation regulated by Aurora A. NuMA undergoes liquid-liquid phase separation during mitotic entry and KifC1 facilitates NuMA condensates concentrating on spindle poles. Phase separation of NuMA is mediated by its C-terminus, whereas its dynein-dynactin binding motif also facilitates this process. Phase-separated NuMA droplets concentrate tubulins, bind microtubules, and enrich crucial regulators, including Kif2A, at the spindle poles, which then depolymerizes spindle microtubules and promotes poleward spindle microtubule flux for spindle assembly and structural dynamics. In this work, we show that NuMA orchestrates mitotic spindle assembly, structural dynamics and function via liquid-liquid phase separation regulated by Aurora A phosphorylation. |
format | Online Article Text |
id | pubmed-8660824 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-86608242021-12-27 NuMA regulates mitotic spindle assembly, structural dynamics and function via phase separation Sun, Mengjie Jia, Mingkang Ren, He Yang, Biying Chi, Wangfei Xin, Guangwei Jiang, Qing Zhang, Chuanmao Nat Commun Article A functional mitotic spindle is essential for accurate chromosome congression and segregation during cell proliferation; however, the underlying mechanisms of its assembly remain unclear. Here we show that NuMA regulates this assembly process via phase separation regulated by Aurora A. NuMA undergoes liquid-liquid phase separation during mitotic entry and KifC1 facilitates NuMA condensates concentrating on spindle poles. Phase separation of NuMA is mediated by its C-terminus, whereas its dynein-dynactin binding motif also facilitates this process. Phase-separated NuMA droplets concentrate tubulins, bind microtubules, and enrich crucial regulators, including Kif2A, at the spindle poles, which then depolymerizes spindle microtubules and promotes poleward spindle microtubule flux for spindle assembly and structural dynamics. In this work, we show that NuMA orchestrates mitotic spindle assembly, structural dynamics and function via liquid-liquid phase separation regulated by Aurora A phosphorylation. Nature Publishing Group UK 2021-12-09 /pmc/articles/PMC8660824/ /pubmed/34887424 http://dx.doi.org/10.1038/s41467-021-27528-6 Text en © The Author(s) 2021 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 Sun, Mengjie Jia, Mingkang Ren, He Yang, Biying Chi, Wangfei Xin, Guangwei Jiang, Qing Zhang, Chuanmao NuMA regulates mitotic spindle assembly, structural dynamics and function via phase separation |
title | NuMA regulates mitotic spindle assembly, structural dynamics and function via phase separation |
title_full | NuMA regulates mitotic spindle assembly, structural dynamics and function via phase separation |
title_fullStr | NuMA regulates mitotic spindle assembly, structural dynamics and function via phase separation |
title_full_unstemmed | NuMA regulates mitotic spindle assembly, structural dynamics and function via phase separation |
title_short | NuMA regulates mitotic spindle assembly, structural dynamics and function via phase separation |
title_sort | numa regulates mitotic spindle assembly, structural dynamics and function via phase separation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8660824/ https://www.ncbi.nlm.nih.gov/pubmed/34887424 http://dx.doi.org/10.1038/s41467-021-27528-6 |
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