Increasing Specificity of Targeted DNA Methylation Editing by Non-Enzymatic CRISPR/dCas9-Based Steric Hindrance.

CRISPR/Cas9 DNA methylation DNMT1 DNMT3A TET1 dCas9 demethylation epigenetic editing steric hindrance

Journal

Biomedicines
ISSN: 2227-9059
Titre abrégé: Biomedicines
Pays: Switzerland
ID NLM: 101691304

Informations de publication

Date de publication:
22 Apr 2023
Historique:
received: 31 03 2023
revised: 19 04 2023
accepted: 20 04 2023
medline: 27 5 2023
pubmed: 27 5 2023
entrez: 27 5 2023
Statut: epublish

Résumé

As advances in genome engineering inch the technology towards wider clinical use-slowed by technical and ethical hurdles-a newer offshoot, termed "epigenome engineering", offers the ability to correct disease-causing changes in the DNA without changing its sequence and, thus, without some of the unfavorable correlates of doing so. In this review, we note some of the shortcomings of epigenetic editing technology-specifically the risks involved in the introduction of epigenetic enzymes-and highlight an alternative epigenetic editing strategy using physical occlusion to modify epigenetic marks at target sites without a requirement for any epigenetic enzyme. This may prove to be a safer alternative for more specific epigenetic editing.

Identifiants

pubmed: 37238909
pii: biomedicines11051238
doi: 10.3390/biomedicines11051238
pmc: PMC10215309
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Subventions

Organisme : CIHR
ID : PJT159583
Pays : Canada

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Auteurs

Daniel M Sapozhnikov (DM)

Department of Pharmacology and Therapeutics, Faculty of Medicine and Health Sciences, McGill University, Montreal, QC H3G 1Y6, Canada.

Moshe Szyf (M)

Department of Pharmacology and Therapeutics, Faculty of Medicine and Health Sciences, McGill University, Montreal, QC H3G 1Y6, Canada.

Classifications MeSH