H3K27M in Gliomas Causes a One-Step Decrease in H3K27 Methylation and Reduced Spreading within the Constraints of H3K36 Methylation.


Journal

Cell reports
ISSN: 2211-1247
Titre abrégé: Cell Rep
Pays: United States
ID NLM: 101573691

Informations de publication

Date de publication:
17 11 2020
Historique:
received: 29 04 2020
revised: 23 09 2020
accepted: 23 10 2020
entrez: 18 11 2020
pubmed: 19 11 2020
medline: 9 11 2021
Statut: ppublish

Résumé

The discovery of H3K27M mutations in pediatric gliomas marked a new chapter in cancer epigenomics. Numerous studies have investigated the effect of this mutation on H3K27 trimethylation, but only recently have we started to realize its additional effects on the epigenome. Here, we use isogenic glioma H3K27M

Identifiants

pubmed: 33207202
pii: S2211-1247(20)31379-6
doi: 10.1016/j.celrep.2020.108390
pmc: PMC7703850
mid: NIHMS1647627
pii:
doi:

Substances chimiques

Chromatin 0
Histones 0
Methionine AE28F7PNPL
Polycomb Repressive Complex 2 EC 2.1.1.43
Lysine K3Z4F929H6

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

108390

Subventions

Organisme : NCI NIH HHS
ID : P01 CA196539
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI118891
Pays : United States

Informations de copyright

Copyright © 2020 The Author(s). Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Interests The authors declare no competing interests.

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Auteurs

Ashot S Harutyunyan (AS)

Department of Human Genetics, McGill University, Montreal, QC H3A 1B1, Canada; Department of Pediatrics, McGill University, Montreal, QC H4A 3J1, Canada; The Research Institute of the McGill University Health Centre, Montreal, QC H4A 3J1, Canada.

Haifen Chen (H)

Department of Human Genetics, McGill University, Montreal, QC H3A 1B1, Canada.

Tianyuan Lu (T)

Department of Human Genetics, McGill University, Montreal, QC H3A 1B1, Canada; Quantitative Life Sciences Program, McGill University, Montreal, QC H3A 2A7, Canada.

Cynthia Horth (C)

Department of Human Genetics, McGill University, Montreal, QC H3A 1B1, Canada.

Hamid Nikbakht (H)

Department of Human Genetics, McGill University, Montreal, QC H3A 1B1, Canada.

Brian Krug (B)

Department of Human Genetics, McGill University, Montreal, QC H3A 1B1, Canada.

Caterina Russo (C)

Department of Pediatrics, McGill University, Montreal, QC H4A 3J1, Canada; The Research Institute of the McGill University Health Centre, Montreal, QC H4A 3J1, Canada.

Eric Bareke (E)

Department of Human Genetics, McGill University, Montreal, QC H3A 1B1, Canada.

Dylan M Marchione (DM)

Department of Biochemistry and Biophysics and the Penn Epigenetics Institute, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.

Mariel Coradin (M)

Department of Biochemistry and Biophysics and the Penn Epigenetics Institute, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.

Benjamin A Garcia (BA)

Department of Biochemistry and Biophysics and the Penn Epigenetics Institute, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.

Nada Jabado (N)

Department of Human Genetics, McGill University, Montreal, QC H3A 1B1, Canada; Department of Pediatrics, McGill University, Montreal, QC H4A 3J1, Canada; The Research Institute of the McGill University Health Centre, Montreal, QC H4A 3J1, Canada. Electronic address: nada.jabado@mcgill.ca.

Jacek Majewski (J)

Department of Human Genetics, McGill University, Montreal, QC H3A 1B1, Canada; McGill Genome Centre, Montreal, QC H3A 0G1, Canada. Electronic address: jacek.majewski@mcgill.ca.

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Classifications MeSH