Assembly principles and stoichiometry of a complete human kinetochore module.


Journal

Science advances
ISSN: 2375-2548
Titre abrégé: Sci Adv
Pays: United States
ID NLM: 101653440

Informations de publication

Date de publication:
06 2021
Historique:
received: 10 12 2020
accepted: 14 05 2021
entrez: 1 7 2021
pubmed: 2 7 2021
medline: 9 4 2022
Statut: epublish

Résumé

Centromeres are epigenetically determined chromosomal loci that seed kinetochore assembly to promote chromosome segregation during cell division. CENP-A, a centromere-specific histone H3 variant, establishes the foundations for centromere epigenetic memory and kinetochore assembly. It recruits the constitutive centromere-associated network (CCAN), which in turn assembles the microtubule-binding interface. How the specific organization of centromeric chromatin relates to kinetochore assembly and to centromere identity through cell division remains conjectural. Here, we break new ground by reconstituting a functional full-length version of CENP-C, the largest human CCAN subunit and a blueprint of kinetochore assembly. We show that full-length CENP-C, a dimer, binds stably to two nucleosomes and permits further assembly of all other kinetochore subunits in vitro with relative ratios closely matching those of endogenous human kinetochores. Our results imply that human kinetochores emerge from clustering multiple copies of a fundamental module and may have important implications for transgenerational inheritance of centromeric chromatin.

Identifiants

pubmed: 34193424
pii: 7/27/eabg1037
doi: 10.1126/sciadv.abg1037
pmc: PMC8245036
pii:
doi:

Substances chimiques

Centromere Protein A 0
Histones 0
Nucleosomes 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC).

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Auteurs

Kai Walstein (K)

Department of Mechanistic Cell Biology, Max Planck Institute of Molecular Physiology, Otto-Hahn-Straße 11, 44227 Dortmund, Germany. kai.walstein@mpi-dortmund.mpg.de andrea.musacchio@mpi-dortmund.mpg.de.
Centre for Medical Biotechnology, Faculty of Biology, University Duisburg-Essen, Universitätsstraße 1, 45141 Essen, Germany.

Arsen Petrovic (A)

Department of Mechanistic Cell Biology, Max Planck Institute of Molecular Physiology, Otto-Hahn-Straße 11, 44227 Dortmund, Germany.

Dongqing Pan (D)

Department of Mechanistic Cell Biology, Max Planck Institute of Molecular Physiology, Otto-Hahn-Straße 11, 44227 Dortmund, Germany.

Birte Hagemeier (B)

Department of Mechanistic Cell Biology, Max Planck Institute of Molecular Physiology, Otto-Hahn-Straße 11, 44227 Dortmund, Germany.

Dorothee Vogt (D)

Department of Mechanistic Cell Biology, Max Planck Institute of Molecular Physiology, Otto-Hahn-Straße 11, 44227 Dortmund, Germany.

Ingrid R Vetter (IR)

Department of Mechanistic Cell Biology, Max Planck Institute of Molecular Physiology, Otto-Hahn-Straße 11, 44227 Dortmund, Germany.

Andrea Musacchio (A)

Department of Mechanistic Cell Biology, Max Planck Institute of Molecular Physiology, Otto-Hahn-Straße 11, 44227 Dortmund, Germany. kai.walstein@mpi-dortmund.mpg.de andrea.musacchio@mpi-dortmund.mpg.de.
Centre for Medical Biotechnology, Faculty of Biology, University Duisburg-Essen, Universitätsstraße 1, 45141 Essen, Germany.

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Classifications MeSH