Centromere/kinetochore is assembled through CENP-C oligomerization.
CCAN
CENP-C
centromere
chromosome segregation
kinetochore assembly
oligomerization
Journal
Molecular cell
ISSN: 1097-4164
Titre abrégé: Mol Cell
Pays: United States
ID NLM: 9802571
Informations de publication
Date de publication:
06 Jul 2023
06 Jul 2023
Historique:
received:
08
08
2022
revised:
04
04
2023
accepted:
16
05
2023
medline:
10
7
2023
pubmed:
10
6
2023
entrez:
9
6
2023
Statut:
ppublish
Résumé
Kinetochore is an essential protein complex required for accurate chromosome segregation. The constitutive centromere-associated network (CCAN), a subcomplex of the kinetochore, associates with centromeric chromatin and provides a platform for the kinetochore assembly. The CCAN protein CENP-C is thought to be a central hub for the centromere/kinetochore organization. However, the role of CENP-C in CCAN assembly needs to be elucidated. Here, we demonstrate that both the CCAN-binding domain and the C-terminal region that includes the Cupin domain of CENP-C are necessary and sufficient for chicken CENP-C function. Structural and biochemical analyses reveal self-oligomerization of the Cupin domains of chicken and human CENP-C. We find that the CENP-C Cupin domain oligomerization is vital for CENP-C function, centromeric localization of CCAN, and centromeric chromatin organization. These results suggest that CENP-C facilitates the centromere/kinetochore assembly through its oligomerization.
Identifiants
pubmed: 37295434
pii: S1097-2765(23)00379-9
doi: 10.1016/j.molcel.2023.05.023
pii:
doi:
Substances chimiques
centromere protein C
0
Chromosomal Proteins, Non-Histone
0
Chromatin
0
Centromere Protein A
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
2188-2205.e13Informations de copyright
Copyright © 2023 The Author(s). Published by Elsevier Inc. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of interests I.J. is an employee of Abberior Instruments, which develops and manufactures super-resolution fluorescence microscopes, including the MINFLUX system used here. All other authors declare no competing interests.