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Yamaguchi, K.* ; Chen, X.* ; Rodgers, B.* ; Miura, F.* ; Bashtrykov, P.* ; Bonhomme, F.* ; Salinas-Luypaert, C.* ; Haxholli, D.* ; Gutekunst, N.* ; Özdemir Aygenli, B. ; Ferry, L.* ; Kirsh, O.* ; Laisné, M.* ; Scelfo, A.* ; Ugur, E.* ; Arimondo, P.B.* ; Leonhardt, H.* ; Kanemaki, M.T.* ; Bartke, T. ; Fachinetti, D.* ; Jeltsch, A.* ; Ito, T.* ; Defossez, P.A.*

Non-canonical functions of UHRF1 maintain DNA methylation homeostasis in cancer cells.

Nat. Commun. 15:2960 (2024)
Verlagsversion DOI PMC
Open Access Gold
Creative Commons Lizenzvertrag
DNA methylation is an essential epigenetic chromatin modification, and its maintenance in mammals requires the protein UHRF1. It is yet unclear if UHRF1 functions solely by stimulating DNA methylation maintenance by DNMT1, or if it has important additional functions. Using degron alleles, we show that UHRF1 depletion causes a much greater loss of DNA methylation than DNMT1 depletion. This is not caused by passive demethylation as UHRF1-depleted cells proliferate more slowly than DNMT1-depleted cells. Instead, bioinformatics, proteomics and genetics experiments establish that UHRF1, besides activating DNMT1, interacts with DNMT3A and DNMT3B and promotes their activity. In addition, we show that UHRF1 antagonizes active DNA demethylation by TET2. Therefore, UHRF1 has non-canonical roles that contribute importantly to DNA methylation homeostasis; these findings have practical implications for epigenetics in health and disease.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Methyltransferase Dnmt1; Protein Uhrf1; Sra Domain; Recognition; Set; Interacts; Base
Sprache englisch
Veröffentlichungsjahr 2024
HGF-Berichtsjahr 2024
ISSN (print) / ISBN 2041-1723
e-ISSN 2041-1723
Zeitschrift Nature Communications
Quellenangaben Band: 15, Heft: 1, Seiten: , Artikelnummer: 2960 Supplement: ,
Verlag Nature Publishing Group
Verlagsort London
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Functional Epigenetics (IFE)
POF Topic(s) 30203 - Molecular Targets and Therapies
Forschungsfeld(er) Helmholtz Diabetes Center
PSP-Element(e) G-502800-001
Förderungen CNRS Epigenetics and Cell Fate Unit
Agence Nationale de la Recherche
Fondation ARC (ARC labellisation program 2019)
Institut National du Cancer
Universit de Paris IdEx
JSPS Overseas Research Fellowships
Platform Project for Supporting Drug Discovery and Life Science Research (Basis for Supporting Innovative Drug Discovery and Life Science Research (BINDS)) from AMED
Deutsche Forschungsgemeinschaft
Foundation DFG
Cell and Tissue Imaging (PICT-IBiSA)
Institut Curie
Region Ile-de-France
Fondation Bettencourt Schueller
Agence Nationale de la Recherche (French National Research Agency)
DOI 10.1038/s41467-024-47314-4
WOS ID 001197889600024
Scopus ID 85189807956
PubMed ID 38580649
Erfassungsdatum 2024-05-24
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