DNA methylation status correlates with adult β-cell regeneration capacity.


Journal

NPJ Regenerative medicine
ISSN: 2057-3995
Titre abrégé: NPJ Regen Med
Pays: United States
ID NLM: 101699846

Informations de publication

Date de publication:
12 Feb 2021
Historique:
received: 15 11 2020
accepted: 14 01 2021
entrez: 13 2 2021
pubmed: 14 2 2021
medline: 14 2 2021
Statut: epublish

Résumé

The role of DNA methylation in β-cell neogenesis is poorly understood. We report that during the process of induced cell reprogramming, methylation content of the Ngn3 and Sox11 genes are diminished. These findings emphasise DNA methylation is a barrier in β-cell regeneration in adulthood, a well described pathophysiological phenomenon of major significance in explaining β-cell deficiency in diabetes in the adult pancreas.

Identifiants

pubmed: 33580013
doi: 10.1038/s41536-021-00119-1
pii: 10.1038/s41536-021-00119-1
pmc: PMC7881134
doi:

Types de publication

Journal Article

Langues

eng

Pagination

7

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Auteurs

Ishant Khurana (I)

Department of Diabetes, Central Clinical School, Monash University, Melbourne, VIC, Australia.
Epigenetics in Human Health and Disease Laboratory, Central Clinical School, Monash University, Melbourne, VIC, Australia.

Keith Al-Hasani (K)

Department of Diabetes, Central Clinical School, Monash University, Melbourne, VIC, Australia. keith.al-hasani@monash.edu.
Epigenetics in Human Health and Disease Laboratory, Central Clinical School, Monash University, Melbourne, VIC, Australia. keith.al-hasani@monash.edu.

Scott Maxwell (S)

Department of Diabetes, Central Clinical School, Monash University, Melbourne, VIC, Australia.
Epigenetics in Human Health and Disease Laboratory, Central Clinical School, Monash University, Melbourne, VIC, Australia.

Harikrishnan K N (H)

Department of Diabetes, Central Clinical School, Monash University, Melbourne, VIC, Australia.
Epigenetics in Human Health and Disease Laboratory, Central Clinical School, Monash University, Melbourne, VIC, Australia.

Jun Okabe (J)

Department of Diabetes, Central Clinical School, Monash University, Melbourne, VIC, Australia.
Epigenetics in Human Health and Disease Laboratory, Central Clinical School, Monash University, Melbourne, VIC, Australia.

Mark E Cooper (ME)

Department of Diabetes, Central Clinical School, Monash University, Melbourne, VIC, Australia.

Patrick Collombat (P)

Université Côte d'Azur, Inserm, CNRS, iBV, Nice, France.

Assam El-Osta (A)

Department of Diabetes, Central Clinical School, Monash University, Melbourne, VIC, Australia. Sam.El-Osta@monash.edu.
Epigenetics in Human Health and Disease Laboratory, Central Clinical School, Monash University, Melbourne, VIC, Australia. Sam.El-Osta@monash.edu.
Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Hong Kong, SAR, Hong Kong. Sam.El-Osta@monash.edu.
Hong Kong Institute of Diabetes and Obesity, Prince of Wales Hospital, The Chinese University of Hong Kong, 3/F Lui Che Woo Clinical Sciences Building, 30-32 Ngan Shing Street, Sha Tin, Hong Kong, SAR, Hong Kong. Sam.El-Osta@monash.edu.
Li Ka Shing Institute of Health Sciences, The Chinese University of Hong Kong, Hong Kong, SAR, Hong Kong. Sam.El-Osta@monash.edu.
University College Copenhagen, Faculty of Health, Department of Technology, Biomedical Laboratory Science, Copenhagen, Denmark. Sam.El-Osta@monash.edu.

Classifications MeSH