Evidence map›Paper›PMID 38123574›Full record

ArticleNature communications2023

USP7/Maged1-mediated H2A monoubiquitination in the paraventricular thalamus: an epigenetic mechanism involved in cocaine use disorder.

Julian Cheron, Leonardo Beccari, Perrine Hagué, Romain Icick, Chloé Despontin, Teresa Carusone, Matthieu Defrance, Sagar Bhogaraju, Elena Martin-Garcia, Roberto Capellan and 4 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.2field-weighted citation impact, top 20% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 8 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 7 institutions in 3 countries.

Julian CheronUniversité Libre de Bruxelles (ULB), ULB Neuroscience Institute, Neurophysiology Laboratory, Brussels, Belgium.ORCID 0000-0001-6369-0019
Leonardo BeccariCentro de Biología Molecular Severo Ochoa, CSIC-UAM, Madrid, Spain.ORCID 0000-0001-6472-5105
Perrine HaguéUniversité Libre de Bruxelles (ULB), ULB Neuroscience Institute, Neurophysiology Laboratory, Brussels, Belgium.
Romain IcickINSERM UMRS_1144, Université Paris Cité, Paris, France.
Chloé DespontinUniversité Libre de Bruxelles (ULB), ULB Neuroscience Institute, Neurophysiology Laboratory, Brussels, Belgium.
Teresa CarusoneEuropean Molecular Biology Laboratory, Grenoble, France.ORCID 0000-0002-4069-2617
Matthieu DefranceInteruniversity Institute of Bioinformatics in Brussels, Université Libre de Bruxelles (ULB), Brussels, Belgium.
Sagar BhogarajuEuropean Molecular Biology Laboratory, Grenoble, France.ORCID 0000-0001-9998-5927
Elena Martin-GarciaLaboratory of Neuropharmacology-Neurophar, Department of Medicine and Life Sciences, Universitat Pompeu Fabra (UPF), Barcelona, Spain.ORCID 0000-0002-4487-3028
Roberto CapellanLaboratory of Neuropharmacology-Neurophar, Department of Medicine and Life Sciences, Universitat Pompeu Fabra (UPF), Barcelona, Spain.ORCID 0000-0001-9586-0684
Rafael MaldonadoLaboratory of Neuropharmacology-Neurophar, Department of Medicine and Life Sciences, Universitat Pompeu Fabra (UPF), Barcelona, Spain.ORCID 0000-0002-4359-8773
Florence VorspanINSERM UMRS_1144, Université Paris Cité, Paris, France.
Jérôme BonnefontUniversité Libre de Bruxelles (ULB), ULB Neuroscience Institute, Institut de Recherches en Biologie Humaine et Moléculaire (IRIBHM), Brussels, Belgium.ORCID 0000-0001-5283-8428
Alban de Kerchove d'ExaerdeUniversité Libre de Bruxelles (ULB), ULB Neuroscience Institute, Neurophysiology Laboratory, Brussels, Belgium. adekerch@ulb.ac.be.ORCID 0000-0002-0682-5877
Université Libre de Bruxelles · BEEuropean Molecular Biology Laboratory · FRInserm · FRUniversitat Pompeu Fabra · ESUniversitat Autònoma de Barcelona · ESUniversité Claude Bernard Lyon 1 · FRWalloon Excellence in Lifesciences and Biotechnology · BE

Funding

Fonds De La Recherche Scientifique - FNRS (Belgian National Fund for Scientific Research) 23587797Fonds De La Recherche Scientifique - FNRS (Belgian National Fund for Scientific Research) 33659288Fonds De La Recherche Scientifique - FNRS (Belgian National Fund for Scientific Research) 33659296
6 · The paper itself

Abstract

The risk of developing drug addiction is strongly influenced by the epigenetic landscape and chromatin remodeling. While histone modifications such as methylation and acetylation have been studied in the ventral tegmental area and nucleus accumbens (NAc), the role of H2A monoubiquitination remains unknown. Our investigations, initially focused on the scaffold protein melanoma-associated antigen D1 (Maged1), reveal that H2A monoubiquitination in the paraventricular thalamus (PVT) significantly contributes to cocaine-adaptive behaviors and transcriptional repression induced by cocaine. Chronic cocaine use increases H2A monoubiquitination, regulated by Maged1 and its partner USP7. Accordingly, Maged1 specific inactivation in thalamic Vglut2 neurons, or USP7 inhibition, blocks cocaine-evoked H2A monoubiquitination and cocaine locomotor sensitization. Additionally, genetic variations in MAGED1 and USP7 are linked to altered susceptibility to cocaine addiction and cocaine-associated symptoms in humans. These findings unveil an epigenetic modification in a non-canonical reward pathway of the brain and a potent marker of epigenetic risk factors for drug addiction in humans.

Indexed as

CocaineCocaine-Related DisordersSubstance-Related DisordersEpigenesis, GeneticHumansNucleus AccumbensThalamusUbiquitin-Specific Peptidase 7CocaineUbiquitin-Specific Peptidase 7USP7 protein, human

Identifiers

PMID38123574
PMCPMC10733359
OpenAlexW4390038738

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.