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  4. Enhancer of Zeste Homolog 2 (EZH2) Contributes to Rod Photoreceptor Death Process in Several Forms of Retinal Degeneration and Its Activity Can Serve as a Biomarker for Therapy Efficacy.
 
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Titre

Enhancer of Zeste Homolog 2 (EZH2) Contributes to Rod Photoreceptor Death Process in Several Forms of Retinal Degeneration and Its Activity Can Serve as a Biomarker for Therapy Efficacy.

Type
article
Institution
UNIL/CHUV/Unisanté + institutions partenaires
Périodique
International Journal of Molecular Sciences  
Auteur(s)
Mbefo, M.
Auteure/Auteur
Berger, A.
Auteure/Auteur
Schouwey, K.
Auteure/Auteur
Gérard, X.
Auteure/Auteur
Kostic, C.
Auteure/Auteur
Beryozkin, A.
Auteure/Auteur
Sharon, D.
Auteure/Auteur
Dolfuss, H.
Auteure/Auteur
Munier, F.
Auteure/Auteur
Tran, H.V.
Auteure/Auteur
van Lohuizen, M.
Auteure/Auteur
Beltran, W.A.
Auteure/Auteur
Arsenijevic, Y.
Auteure/Auteur
Liens vers les personnes
Kostic Bensadoun, Corinne  
Munier, Francis  
Arsenijevic, Yvan  
Mbefo, Martial  
Tran, Hoai Viet  
Gérard, Xavier  
Berger, Adeline  
Liens vers les unités
Hôpital ophtalmique Jules Gonin  
Ophtalmologie  
ISSN
1422-0067
Statut éditorial
Publié
Date de publication
2021-08-28
Volume
22
Numéro
17
Première page
9331
Peer-reviewed
Oui
Langue
anglais
Notes
Publication types: Journal Article
Publication Status: epublish
Résumé
Inherited retinal dystrophies (IRD) are due to various gene mutations. Each mutated gene instigates a specific cell homeostasis disruption, leading to a modification in gene expression and retinal degeneration. We previously demonstrated that the polycomb-repressive complex-1 (PRC1) markedly contributes to the cell death process. To better understand these mechanisms, we herein study the role of PRC2, specifically EZH2, which often initiates the gene inhibition by PRC1. We observed that the epigenetic mark H3K27me3 generated by EZH2 was progressively and strongly expressed in some individual photoreceptors and that the H3K27me3-positive cell number increased before cell death. H3K27me3 accumulation occurs between early (accumulation of cGMP) and late (CDK4 expression) events of retinal degeneration. EZH2 hyperactivity was observed in four recessive and two dominant mouse models of retinal degeneration, as well as two dog models and one IRD patient. Acute pharmacological EZH2 inhibition by intravitreal injection decreased the appearance of H3K27me3 marks and the number of TUNEL-positive cells revealing that EZH2 contributes to the cell death process. Finally, we observed that the absence of the H3K27me3 mark is a biomarker of gene therapy treatment efficacy in XLRPA2 dog model. PRC2 and PRC1 are therefore important actors in the degenerative process of multiple forms of IRD.
Sujets

Animals

DNA Methylation

Dogs

Enhancer of Zeste Hom...

Enhancer of Zeste Hom...

Epigenesis, Genetic

Eye Proteins/physiolo...

Histones/genetics

Histones/metabolism

Humans

Mice

Mice, Inbred C57BL

Mice, Knockout

Polycomb Repressive C...

Proto-Oncogene Protei...

Retinal Degeneration/...

Retinal Degeneration/...

Retinal Degeneration/...

Retinal Rod Photorece...

Retinal Rod Photorece...

Retinitis Pigmentosa/...

Retinitis Pigmentosa/...

Retinitis Pigmentosa/...

epigenetic

neuroprotection

polycomb-repressive c...

retinal degeneration

PID Serval
serval:BIB_CD3CAE19D3B7
DOI
10.3390/ijms22179331
PMID
34502238
WOS
000694303300001
Permalien
https://iris.unil.ch/handle/iris/174526
Open Access
Oui
Date de création
2021-09-21T12:03:39.187Z
Date de création dans IRIS
2025-05-21T00:27:11Z
Fichier(s)
En cours de chargement...
Vignette d'image
Nom

34502238_BIB_CD3CAE19D3B7.pdf

Version du manuscrit

published

Licence

https://creativecommons.org/licenses/by/4.0

Taille

3.48 MB

Format

Adobe PDF

PID Serval

serval:BIB_CD3CAE19D3B7.P001

URN

urn:nbn:ch:serval-BIB_CD3CAE19D3B75

Somme de contrôle

(MD5):ba237659c1d2000e790f627717bc1c35

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