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The Ndc80 complex bridges two Dam1 complex rings
Strong kinetochore-microtubule attachments are essential for faithful segregation of sister chromatids during mitosis. The Dam1 and Ndc80 complexes are the main microtubule binding components of the Saccharomyces cerevisiae kinetochore. Cooperation between these two complexes enhances kinetochore-mi...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5354518/ https://www.ncbi.nlm.nih.gov/pubmed/28191870 http://dx.doi.org/10.7554/eLife.21069 |
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author | Kim, Jae ook Zelter, Alex Umbreit, Neil T Bollozos, Athena Riffle, Michael Johnson, Richard MacCoss, Michael J Asbury, Charles L Davis, Trisha N |
author_facet | Kim, Jae ook Zelter, Alex Umbreit, Neil T Bollozos, Athena Riffle, Michael Johnson, Richard MacCoss, Michael J Asbury, Charles L Davis, Trisha N |
author_sort | Kim, Jae ook |
collection | PubMed |
description | Strong kinetochore-microtubule attachments are essential for faithful segregation of sister chromatids during mitosis. The Dam1 and Ndc80 complexes are the main microtubule binding components of the Saccharomyces cerevisiae kinetochore. Cooperation between these two complexes enhances kinetochore-microtubule coupling and is regulated by Aurora B kinase. We show that the Ndc80 complex can simultaneously bind and bridge across two Dam1 complex rings through a tripartite interaction, each component of which is regulated by Aurora B kinase. Mutations in any one of the Ndc80p interaction regions abrogates the Ndc80 complex’s ability to bind two Dam1 rings in vitro, and results in kinetochore biorientation and microtubule attachment defects in vivo. We also show that an extra-long Ndc80 complex, engineered to space the two Dam1 rings further apart, does not support growth. Taken together, our work suggests that each kinetochore in vivo contains two Dam1 rings and that proper spacing between the rings is vital. DOI: http://dx.doi.org/10.7554/eLife.21069.001 |
format | Online Article Text |
id | pubmed-5354518 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-53545182017-03-17 The Ndc80 complex bridges two Dam1 complex rings Kim, Jae ook Zelter, Alex Umbreit, Neil T Bollozos, Athena Riffle, Michael Johnson, Richard MacCoss, Michael J Asbury, Charles L Davis, Trisha N eLife Biochemistry Strong kinetochore-microtubule attachments are essential for faithful segregation of sister chromatids during mitosis. The Dam1 and Ndc80 complexes are the main microtubule binding components of the Saccharomyces cerevisiae kinetochore. Cooperation between these two complexes enhances kinetochore-microtubule coupling and is regulated by Aurora B kinase. We show that the Ndc80 complex can simultaneously bind and bridge across two Dam1 complex rings through a tripartite interaction, each component of which is regulated by Aurora B kinase. Mutations in any one of the Ndc80p interaction regions abrogates the Ndc80 complex’s ability to bind two Dam1 rings in vitro, and results in kinetochore biorientation and microtubule attachment defects in vivo. We also show that an extra-long Ndc80 complex, engineered to space the two Dam1 rings further apart, does not support growth. Taken together, our work suggests that each kinetochore in vivo contains two Dam1 rings and that proper spacing between the rings is vital. DOI: http://dx.doi.org/10.7554/eLife.21069.001 eLife Sciences Publications, Ltd 2017-02-13 /pmc/articles/PMC5354518/ /pubmed/28191870 http://dx.doi.org/10.7554/eLife.21069 Text en © 2017, Kim et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Biochemistry Kim, Jae ook Zelter, Alex Umbreit, Neil T Bollozos, Athena Riffle, Michael Johnson, Richard MacCoss, Michael J Asbury, Charles L Davis, Trisha N The Ndc80 complex bridges two Dam1 complex rings |
title | The Ndc80 complex bridges two Dam1 complex rings |
title_full | The Ndc80 complex bridges two Dam1 complex rings |
title_fullStr | The Ndc80 complex bridges two Dam1 complex rings |
title_full_unstemmed | The Ndc80 complex bridges two Dam1 complex rings |
title_short | The Ndc80 complex bridges two Dam1 complex rings |
title_sort | ndc80 complex bridges two dam1 complex rings |
topic | Biochemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5354518/ https://www.ncbi.nlm.nih.gov/pubmed/28191870 http://dx.doi.org/10.7554/eLife.21069 |
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