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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...

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Autores principales: 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
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2010
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.
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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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