Glucose Regulates m 6 A Methylation of RNA in Pancreatic Islets.

Autor: Bornaque F; Institut Pasteur de Lille, University of Lille, Inserm, CHU Lille, CNRS, U1283-UMR 8199-EGID, F-59000 Lille, France., Delannoy CP; Institut Pasteur de Lille, University of Lille, Inserm, CHU Lille, CNRS, U1283-UMR 8199-EGID, F-59000 Lille, France., Courty E; Institut Pasteur de Lille, University of Lille, Inserm, CHU Lille, CNRS, U1283-UMR 8199-EGID, F-59000 Lille, France., Rabhi N; Institut Pasteur de Lille, University of Lille, Inserm, CHU Lille, CNRS, U1283-UMR 8199-EGID, F-59000 Lille, France., Carney C; Institut Pasteur de Lille, University of Lille, Inserm, CHU Lille, CNRS, U1283-UMR 8199-EGID, F-59000 Lille, France., Rolland L; Institut Pasteur de Lille, University of Lille, Inserm, CHU Lille, CNRS, U1283-UMR 8199-EGID, F-59000 Lille, France., Moreno M; Institut Pasteur de Lille, University of Lille, Inserm, CHU Lille, CNRS, U1283-UMR 8199-EGID, F-59000 Lille, France., Gromada X; Institut Pasteur de Lille, University of Lille, Inserm, CHU Lille, CNRS, U1283-UMR 8199-EGID, F-59000 Lille, France., Bourouh C; Institut Pasteur de Lille, University of Lille, Inserm, CHU Lille, CNRS, U1283-UMR 8199-EGID, F-59000 Lille, France., Petit P; University of Lille, Inserm, CHU Lille, U1190-EGID, F-59000 Lille, France., Durand E; Institut Pasteur de Lille, University of Lille, Inserm, CHU Lille, CNRS, U1283-UMR 8199-EGID, F-59000 Lille, France., Pattou F; University of Lille, Inserm, CHU Lille, U1190-EGID, F-59000 Lille, France., Kerr-Conte J; University of Lille, Inserm, CHU Lille, U1190-EGID, F-59000 Lille, France., Froguel P; Institut Pasteur de Lille, University of Lille, Inserm, CHU Lille, CNRS, U1283-UMR 8199-EGID, F-59000 Lille, France., Bonnefond A; Institut Pasteur de Lille, University of Lille, Inserm, CHU Lille, CNRS, U1283-UMR 8199-EGID, F-59000 Lille, France., Oger F; Institut Pasteur de Lille, University of Lille, Inserm, CHU Lille, CNRS, U1283-UMR 8199-EGID, F-59000 Lille, France., Annicotte JS; Institut Pasteur de Lille, University of Lille, Inserm, CHU Lille, CNRS, U1283-UMR 8199-EGID, F-59000 Lille, France.
Jazyk: angličtina
Zdroj: Cells [Cells] 2022 Jan 15; Vol. 11 (2). Date of Electronic Publication: 2022 Jan 15.
DOI: 10.3390/cells11020291
Abstrakt: Type 2 diabetes is characterized by chronic hyperglycemia associated with impaired insulin action and secretion. Although the heritability of type 2 diabetes is high, the environment, including blood components, could play a major role in the development of the disease. Amongst environmental effects, epitranscriptomic modifications have been recently shown to affect gene expression and glucose homeostasis. The epitranscriptome is characterized by reversible chemical changes in RNA, with one of the most prevalent being the m 6 A methylation of RNA. Since pancreatic β cells fine tune glucose levels and play a major role in type 2 diabetes physiopathology, we hypothesized that the environment, through variations in blood glucose or blood free fatty acid concentrations, could induce changes in m 6 A methylation of RNAs in pancreatic β cells. Here we observe a significant decrease in m 6 A methylation upon high glucose concentration, both in mice and human islets, associated with altered expression levels of m 6 A demethylases. In addition, the use of siRNA and/or specific inhibitors against selected m 6 A enzymes demonstrate that these enzymes modulate the expression of genes involved in pancreatic β-cell identity and glucose-stimulated insulin secretion. Our data suggest that environmental variations, such as glucose, control m 6 A methylation in pancreatic β cells, playing a key role in the control of gene expression and pancreatic β-cell functions. Our results highlight novel causes and new mechanisms potentially involved in type 2 diabetes physiopathology and may contribute to a better understanding of the etiology of this disease.
Databáze: MEDLINE
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