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Thamkachy, R.* ; Medina-Pritchard, B.* ; Park, S.H.* ; Chiodi, C.G.* ; Zou, J.* ; de la Torre-Barranco, M.* ; Shimanaka, K.* ; Abad, M.A.* ; Gallego Páramo, C.* ; Feederle, R. ; Ruksenaite, E.* ; Heun, P.* ; Davies, O.R.* ; Rappsilber, J.* ; Schneidman-Duhovny, D.* ; Cho, U.S.* ; Jeyaprakash, A.A.*

Structural basis for Mis18 complex assembly and its implications for centromere maintenance.

EMBO Rep., DOI: 10.1038/s44319-024-00183-w (2024)
Verlagsversion DOI PMC
Open Access Hybrid
Creative Commons Lizenzvertrag
The centromere, defined by the enrichment of CENP-A (a Histone H3 variant) containing nucleosomes, is a specialised chromosomal locus that acts as a microtubule attachment site. To preserve centromere identity, CENP-A levels must be maintained through active CENP-A loading during the cell cycle. A central player mediating this process is the Mis18 complex (Mis18α, Mis18β and Mis18BP1), which recruits the CENP-A-specific chaperone HJURP to centromeres for CENP-A deposition. Here, using a multi-pronged approach, we characterise the structure of the Mis18 complex and show that multiple hetero- and homo-oligomeric interfaces facilitate the hetero-octameric Mis18 complex assembly composed of 4 Mis18α, 2 Mis18β and 2 Mis18BP1. Evaluation of structure-guided/separation-of-function mutants reveals structural determinants essential for cell cycle controlled Mis18 complex assembly and centromere maintenance. Our results provide new mechanistic insights on centromere maintenance, highlighting that while Mis18α can associate with centromeres and deposit CENP-A independently of Mis18β, the latter is indispensable for the optimal level of CENP-A loading required for preserving the centromere identity.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Cenp-a ; Centromere ; Centromere Inheritance ; Integrative Structural Analysis ; Mis18 Complex; Cenp-a Chromatin; Dna-binding; Recruitment; Domain; Recognition; Hjurp; Tools; Propagation; Nucleosomes; Deposition
Sprache englisch
Veröffentlichungsjahr 2024
HGF-Berichtsjahr 2024
ISSN (print) / ISBN 1469-221X
e-ISSN 1469-3178
Zeitschrift EMBO Reports
Verlag EMBO Press
Verlagsort Campus, 4 Crinan St, London, N1 9xw, England
Begutachtungsstatus Peer reviewed
Institut(e) CF Monoclonal Antibodies (CF-MAB)
POF Topic(s) 30201 - Metabolic Health
PSP-Element(e) A-631900-001
Förderungen Israeli Ministry of Science and Technology
Centre Core Grant
Wellcome Trust Centre for Cell Biology
European Union
Medical Research Council (MRC, United Kingdom)
NIH
ISF
Senior Research Fellowships
DOI 10.1038/s44319-024-00183-w
WOS ID 001260406200001
Scopus ID 85197315486
PubMed ID 38951710
Erfassungsdatum 2024-07-24
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