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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...

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Autores principales: Sun, Mengjie, Jia, Mingkang, Ren, He, Yang, Biying, Chi, Wangfei, Xin, Guangwei, Jiang, Qing, Zhang, Chuanmao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
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.
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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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