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The MIS12 complex is a protein interaction hub for outer kinetochore assembly
Kinetochores are nucleoprotein assemblies responsible for the attachment of chromosomes to spindle microtubules during mitosis. The KMN network, a crucial constituent of the outer kinetochore, creates an interface that connects microtubules to centromeric chromatin. The NDC80, MIS12, and KNL1 comple...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2935574/ https://www.ncbi.nlm.nih.gov/pubmed/20819937 http://dx.doi.org/10.1083/jcb.201002070 |
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author | Petrovic, Arsen Pasqualato, Sebastiano Dube, Prakash Krenn, Veronica Santaguida, Stefano Cittaro, Davide Monzani, Silvia Massimiliano, Lucia Keller, Jenny Tarricone, Aldo Maiolica, Alessio Stark, Holger Musacchio, Andrea |
author_facet | Petrovic, Arsen Pasqualato, Sebastiano Dube, Prakash Krenn, Veronica Santaguida, Stefano Cittaro, Davide Monzani, Silvia Massimiliano, Lucia Keller, Jenny Tarricone, Aldo Maiolica, Alessio Stark, Holger Musacchio, Andrea |
author_sort | Petrovic, Arsen |
collection | PubMed |
description | Kinetochores are nucleoprotein assemblies responsible for the attachment of chromosomes to spindle microtubules during mitosis. The KMN network, a crucial constituent of the outer kinetochore, creates an interface that connects microtubules to centromeric chromatin. The NDC80, MIS12, and KNL1 complexes form the core of the KMN network. We recently reported the structural organization of the human NDC80 complex. In this study, we extend our analysis to the human MIS12 complex and show that it has an elongated structure with a long axis of ∼22 nm. Through biochemical analysis, cross-linking–based methods, and negative-stain electron microscopy, we investigated the reciprocal organization of the subunits of the MIS12 complex and their contacts with the rest of the KMN network. A highlight of our findings is the identification of the NSL1 subunit as a scaffold supporting interactions of the MIS12 complex with the NDC80 and KNL1 complexes. Our analysis has important implications for understanding kinetochore organization in different organisms. |
format | Text |
id | pubmed-2935574 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-29355742011-03-06 The MIS12 complex is a protein interaction hub for outer kinetochore assembly Petrovic, Arsen Pasqualato, Sebastiano Dube, Prakash Krenn, Veronica Santaguida, Stefano Cittaro, Davide Monzani, Silvia Massimiliano, Lucia Keller, Jenny Tarricone, Aldo Maiolica, Alessio Stark, Holger Musacchio, Andrea J Cell Biol Research Articles Kinetochores are nucleoprotein assemblies responsible for the attachment of chromosomes to spindle microtubules during mitosis. The KMN network, a crucial constituent of the outer kinetochore, creates an interface that connects microtubules to centromeric chromatin. The NDC80, MIS12, and KNL1 complexes form the core of the KMN network. We recently reported the structural organization of the human NDC80 complex. In this study, we extend our analysis to the human MIS12 complex and show that it has an elongated structure with a long axis of ∼22 nm. Through biochemical analysis, cross-linking–based methods, and negative-stain electron microscopy, we investigated the reciprocal organization of the subunits of the MIS12 complex and their contacts with the rest of the KMN network. A highlight of our findings is the identification of the NSL1 subunit as a scaffold supporting interactions of the MIS12 complex with the NDC80 and KNL1 complexes. Our analysis has important implications for understanding kinetochore organization in different organisms. The Rockefeller University Press 2010-09-06 /pmc/articles/PMC2935574/ /pubmed/20819937 http://dx.doi.org/10.1083/jcb.201002070 Text en © 2010 Petrovic et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Research Articles Petrovic, Arsen Pasqualato, Sebastiano Dube, Prakash Krenn, Veronica Santaguida, Stefano Cittaro, Davide Monzani, Silvia Massimiliano, Lucia Keller, Jenny Tarricone, Aldo Maiolica, Alessio Stark, Holger Musacchio, Andrea The MIS12 complex is a protein interaction hub for outer kinetochore assembly |
title | The MIS12 complex is a protein interaction hub for outer kinetochore assembly |
title_full | The MIS12 complex is a protein interaction hub for outer kinetochore assembly |
title_fullStr | The MIS12 complex is a protein interaction hub for outer kinetochore assembly |
title_full_unstemmed | The MIS12 complex is a protein interaction hub for outer kinetochore assembly |
title_short | The MIS12 complex is a protein interaction hub for outer kinetochore assembly |
title_sort | mis12 complex is a protein interaction hub for outer kinetochore assembly |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2935574/ https://www.ncbi.nlm.nih.gov/pubmed/20819937 http://dx.doi.org/10.1083/jcb.201002070 |
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