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EB1 regulates attachment of Ska1 with microtubules by forming extended structures on the microtubule lattice
Kinetochore couples chromosome movement to dynamic microtubules, a process that is fundamental to mitosis in all eukaryotes but poorly understood. In vertebrates, spindle-kinetochore-associated (Ska1–3) protein complex plays an important role in this process. However, the proteins that stabilize Ska...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4894954/ https://www.ncbi.nlm.nih.gov/pubmed/27225956 http://dx.doi.org/10.1038/ncomms11665 |
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author | Thomas, Geethu E. Bandopadhyay, K. Sutradhar, Sabyasachi Renjith, M. R. Singh, Puja Gireesh, K. K. Simon, Steny Badarudeen, Binshad Gupta, Hindol Banerjee, Manidipa Paul, Raja Mitra, J. Manna, Tapas K. |
author_facet | Thomas, Geethu E. Bandopadhyay, K. Sutradhar, Sabyasachi Renjith, M. R. Singh, Puja Gireesh, K. K. Simon, Steny Badarudeen, Binshad Gupta, Hindol Banerjee, Manidipa Paul, Raja Mitra, J. Manna, Tapas K. |
author_sort | Thomas, Geethu E. |
collection | PubMed |
description | Kinetochore couples chromosome movement to dynamic microtubules, a process that is fundamental to mitosis in all eukaryotes but poorly understood. In vertebrates, spindle-kinetochore-associated (Ska1–3) protein complex plays an important role in this process. However, the proteins that stabilize Ska-mediated kinetochore-microtubule attachment remain unknown. Here we show that microtubule plus-end tracking protein EB1 facilitates Ska localization on microtubules in vertebrate cells. EB1 depletion results in a significant reduction of Ska1 recruitment onto microtubules and defects in mitotic chromosome alignment, which is also reflected in computational modelling. Biochemical experiments reveal that EB1 interacts with Ska1, facilitates Ska1-microtubule attachment and together stabilizes microtubules. Structural studies reveal that EB1 either with Ska1 or Ska complex forms extended structures on microtubule lattice. Results indicate that EB1 promotes Ska association with K-fibres and facilitates kinetochore-microtubule attachment. They also implicate that in vertebrates, chromosome coupling to dynamic microtubules could be mediated through EB1-Ska extended structures. |
format | Online Article Text |
id | pubmed-4894954 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48949542016-06-21 EB1 regulates attachment of Ska1 with microtubules by forming extended structures on the microtubule lattice Thomas, Geethu E. Bandopadhyay, K. Sutradhar, Sabyasachi Renjith, M. R. Singh, Puja Gireesh, K. K. Simon, Steny Badarudeen, Binshad Gupta, Hindol Banerjee, Manidipa Paul, Raja Mitra, J. Manna, Tapas K. Nat Commun Article Kinetochore couples chromosome movement to dynamic microtubules, a process that is fundamental to mitosis in all eukaryotes but poorly understood. In vertebrates, spindle-kinetochore-associated (Ska1–3) protein complex plays an important role in this process. However, the proteins that stabilize Ska-mediated kinetochore-microtubule attachment remain unknown. Here we show that microtubule plus-end tracking protein EB1 facilitates Ska localization on microtubules in vertebrate cells. EB1 depletion results in a significant reduction of Ska1 recruitment onto microtubules and defects in mitotic chromosome alignment, which is also reflected in computational modelling. Biochemical experiments reveal that EB1 interacts with Ska1, facilitates Ska1-microtubule attachment and together stabilizes microtubules. Structural studies reveal that EB1 either with Ska1 or Ska complex forms extended structures on microtubule lattice. Results indicate that EB1 promotes Ska association with K-fibres and facilitates kinetochore-microtubule attachment. They also implicate that in vertebrates, chromosome coupling to dynamic microtubules could be mediated through EB1-Ska extended structures. Nature Publishing Group 2016-05-26 /pmc/articles/PMC4894954/ /pubmed/27225956 http://dx.doi.org/10.1038/ncomms11665 Text en Copyright © 2016, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Thomas, Geethu E. Bandopadhyay, K. Sutradhar, Sabyasachi Renjith, M. R. Singh, Puja Gireesh, K. K. Simon, Steny Badarudeen, Binshad Gupta, Hindol Banerjee, Manidipa Paul, Raja Mitra, J. Manna, Tapas K. EB1 regulates attachment of Ska1 with microtubules by forming extended structures on the microtubule lattice |
title | EB1 regulates attachment of Ska1 with microtubules by forming extended structures on the microtubule lattice |
title_full | EB1 regulates attachment of Ska1 with microtubules by forming extended structures on the microtubule lattice |
title_fullStr | EB1 regulates attachment of Ska1 with microtubules by forming extended structures on the microtubule lattice |
title_full_unstemmed | EB1 regulates attachment of Ska1 with microtubules by forming extended structures on the microtubule lattice |
title_short | EB1 regulates attachment of Ska1 with microtubules by forming extended structures on the microtubule lattice |
title_sort | eb1 regulates attachment of ska1 with microtubules by forming extended structures on the microtubule lattice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4894954/ https://www.ncbi.nlm.nih.gov/pubmed/27225956 http://dx.doi.org/10.1038/ncomms11665 |
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