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The binding of Borealin to microtubules underlies a tension independent kinetochore-microtubule error correction pathway
Proper chromosome segregation depends upon kinetochore phosphorylation by the Chromosome Passenger Complex (CPC). Current models suggest the activity of the CPC decreases in response to the inter-kinetochore stretch that accompanies the formation of bi-oriented microtubule attachments, however littl...
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/PMC6368601/ https://www.ncbi.nlm.nih.gov/pubmed/30737408 http://dx.doi.org/10.1038/s41467-019-08418-4 |
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author | Trivedi, Prasad Zaytsev, Anatoly V. Godzi, Maxim Ataullakhanov, Fazly I. Grishchuk, Ekaterina L. Stukenberg, P. Todd |
author_facet | Trivedi, Prasad Zaytsev, Anatoly V. Godzi, Maxim Ataullakhanov, Fazly I. Grishchuk, Ekaterina L. Stukenberg, P. Todd |
author_sort | Trivedi, Prasad |
collection | PubMed |
description | Proper chromosome segregation depends upon kinetochore phosphorylation by the Chromosome Passenger Complex (CPC). Current models suggest the activity of the CPC decreases in response to the inter-kinetochore stretch that accompanies the formation of bi-oriented microtubule attachments, however little is known about tension-independent CPC phosphoregulation. Microtubule bundles initially lie in close proximity to inner centromeres and become depleted by metaphase. Here we find these microtubules control kinetochore phosphorylation by the CPC in a tension independent manner via a microtubule-binding site on the Borealin subunit. Disruption of Borealin-microtubule interactions generates reduced phosphorylation of prometaphase kinetochores, improper kinetochore-microtubule attachments and weakened spindle checkpoint signals. Experimental and modeling evidence suggests that kinetochore phosphorylation is greatly stimulated when the CPC binds microtubules that lie near the inner centromere, even if kinetochores have high inter-kinetochore stretch. We propose the CPC senses its local environment through microtubule structures to control phosphorylation of kinetochores. |
format | Online Article Text |
id | pubmed-6368601 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-63686012019-02-11 The binding of Borealin to microtubules underlies a tension independent kinetochore-microtubule error correction pathway Trivedi, Prasad Zaytsev, Anatoly V. Godzi, Maxim Ataullakhanov, Fazly I. Grishchuk, Ekaterina L. Stukenberg, P. Todd Nat Commun Article Proper chromosome segregation depends upon kinetochore phosphorylation by the Chromosome Passenger Complex (CPC). Current models suggest the activity of the CPC decreases in response to the inter-kinetochore stretch that accompanies the formation of bi-oriented microtubule attachments, however little is known about tension-independent CPC phosphoregulation. Microtubule bundles initially lie in close proximity to inner centromeres and become depleted by metaphase. Here we find these microtubules control kinetochore phosphorylation by the CPC in a tension independent manner via a microtubule-binding site on the Borealin subunit. Disruption of Borealin-microtubule interactions generates reduced phosphorylation of prometaphase kinetochores, improper kinetochore-microtubule attachments and weakened spindle checkpoint signals. Experimental and modeling evidence suggests that kinetochore phosphorylation is greatly stimulated when the CPC binds microtubules that lie near the inner centromere, even if kinetochores have high inter-kinetochore stretch. We propose the CPC senses its local environment through microtubule structures to control phosphorylation of kinetochores. Nature Publishing Group UK 2019-02-08 /pmc/articles/PMC6368601/ /pubmed/30737408 http://dx.doi.org/10.1038/s41467-019-08418-4 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 Trivedi, Prasad Zaytsev, Anatoly V. Godzi, Maxim Ataullakhanov, Fazly I. Grishchuk, Ekaterina L. Stukenberg, P. Todd The binding of Borealin to microtubules underlies a tension independent kinetochore-microtubule error correction pathway |
title | The binding of Borealin to microtubules underlies a tension independent kinetochore-microtubule error correction pathway |
title_full | The binding of Borealin to microtubules underlies a tension independent kinetochore-microtubule error correction pathway |
title_fullStr | The binding of Borealin to microtubules underlies a tension independent kinetochore-microtubule error correction pathway |
title_full_unstemmed | The binding of Borealin to microtubules underlies a tension independent kinetochore-microtubule error correction pathway |
title_short | The binding of Borealin to microtubules underlies a tension independent kinetochore-microtubule error correction pathway |
title_sort | binding of borealin to microtubules underlies a tension independent kinetochore-microtubule error correction pathway |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6368601/ https://www.ncbi.nlm.nih.gov/pubmed/30737408 http://dx.doi.org/10.1038/s41467-019-08418-4 |
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