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LUBAC controls chromosome alignment by targeting CENP-E to attached kinetochores

Faithful chromosome segregation requires proper chromosome congression at prometaphase and dynamic maintenance of the aligned chromosomes at metaphase. Chromosome missegregation can result in aneuploidy, birth defects and cancer. The kinetochore-bound KMN network and the kinesin motor CENP-E are cri...

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Autores principales: Wu, Min, Chang, Yan, Hu, Huaibin, Mu, Rui, Zhang, Yucheng, Qin, Xuanhe, Duan, Xiaotao, Li, Weihua, Tu, Haiqing, Zhang, Weina, Wang, Guang, Han, Qiuying, Li, Ailing, Zhou, Tao, Iwai, Kazuhiro, Zhang, Xuemin, Li, Huiyan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6336796/
https://www.ncbi.nlm.nih.gov/pubmed/30655516
http://dx.doi.org/10.1038/s41467-018-08043-7
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author Wu, Min
Chang, Yan
Hu, Huaibin
Mu, Rui
Zhang, Yucheng
Qin, Xuanhe
Duan, Xiaotao
Li, Weihua
Tu, Haiqing
Zhang, Weina
Wang, Guang
Han, Qiuying
Li, Ailing
Zhou, Tao
Iwai, Kazuhiro
Zhang, Xuemin
Li, Huiyan
author_facet Wu, Min
Chang, Yan
Hu, Huaibin
Mu, Rui
Zhang, Yucheng
Qin, Xuanhe
Duan, Xiaotao
Li, Weihua
Tu, Haiqing
Zhang, Weina
Wang, Guang
Han, Qiuying
Li, Ailing
Zhou, Tao
Iwai, Kazuhiro
Zhang, Xuemin
Li, Huiyan
author_sort Wu, Min
collection PubMed
description Faithful chromosome segregation requires proper chromosome congression at prometaphase and dynamic maintenance of the aligned chromosomes at metaphase. Chromosome missegregation can result in aneuploidy, birth defects and cancer. The kinetochore-bound KMN network and the kinesin motor CENP-E are critical for kinetochore-microtubule attachment and chromosome stability. The linear ubiquitin chain assembly complex (LUBAC) attaches linear ubiquitin chains to substrates, with well-established roles in immune response. Here, we identify LUBAC as a key player of chromosome alignment during mitosis. LUBAC catalyzes linear ubiquitination of the kinetochore motor CENP-E, which is specifically required for the localization of CENP-E at attached kinetochores, but not unattached ones. KNL1 acts as a receptor of linear ubiquitin chains to anchor CENP-E at attached kinetochores in prometaphase and metaphase. Thus, linear ubiquitination promotes chromosome congression and dynamic chromosome alignment by coupling the dynamic kinetochore microtubule receptor CENP-E to the static one, the KMN network.
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spelling pubmed-63367962019-01-22 LUBAC controls chromosome alignment by targeting CENP-E to attached kinetochores Wu, Min Chang, Yan Hu, Huaibin Mu, Rui Zhang, Yucheng Qin, Xuanhe Duan, Xiaotao Li, Weihua Tu, Haiqing Zhang, Weina Wang, Guang Han, Qiuying Li, Ailing Zhou, Tao Iwai, Kazuhiro Zhang, Xuemin Li, Huiyan Nat Commun Article Faithful chromosome segregation requires proper chromosome congression at prometaphase and dynamic maintenance of the aligned chromosomes at metaphase. Chromosome missegregation can result in aneuploidy, birth defects and cancer. The kinetochore-bound KMN network and the kinesin motor CENP-E are critical for kinetochore-microtubule attachment and chromosome stability. The linear ubiquitin chain assembly complex (LUBAC) attaches linear ubiquitin chains to substrates, with well-established roles in immune response. Here, we identify LUBAC as a key player of chromosome alignment during mitosis. LUBAC catalyzes linear ubiquitination of the kinetochore motor CENP-E, which is specifically required for the localization of CENP-E at attached kinetochores, but not unattached ones. KNL1 acts as a receptor of linear ubiquitin chains to anchor CENP-E at attached kinetochores in prometaphase and metaphase. Thus, linear ubiquitination promotes chromosome congression and dynamic chromosome alignment by coupling the dynamic kinetochore microtubule receptor CENP-E to the static one, the KMN network. Nature Publishing Group UK 2019-01-17 /pmc/articles/PMC6336796/ /pubmed/30655516 http://dx.doi.org/10.1038/s41467-018-08043-7 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
Wu, Min
Chang, Yan
Hu, Huaibin
Mu, Rui
Zhang, Yucheng
Qin, Xuanhe
Duan, Xiaotao
Li, Weihua
Tu, Haiqing
Zhang, Weina
Wang, Guang
Han, Qiuying
Li, Ailing
Zhou, Tao
Iwai, Kazuhiro
Zhang, Xuemin
Li, Huiyan
LUBAC controls chromosome alignment by targeting CENP-E to attached kinetochores
title LUBAC controls chromosome alignment by targeting CENP-E to attached kinetochores
title_full LUBAC controls chromosome alignment by targeting CENP-E to attached kinetochores
title_fullStr LUBAC controls chromosome alignment by targeting CENP-E to attached kinetochores
title_full_unstemmed LUBAC controls chromosome alignment by targeting CENP-E to attached kinetochores
title_short LUBAC controls chromosome alignment by targeting CENP-E to attached kinetochores
title_sort lubac controls chromosome alignment by targeting cenp-e to attached kinetochores
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6336796/
https://www.ncbi.nlm.nih.gov/pubmed/30655516
http://dx.doi.org/10.1038/s41467-018-08043-7
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