A circular RNA generated from an intron of the insulin gene controls insulin secretion.
Lisa StollAdriana Rodríguez-TrejoClaudiane GuayFlora BrozziMustafa Bilal BayazitSonia GattescoVéronique MenoudJonathan SobelAna Claudia MarquesMorten Trillingsgaard VenøJonathan Lou S EsguerraMohammad BarghouthMara SuleimanLorella MarselliJørgen KjemsLena EliassonErik RenströmKarim BouzakriMichel PingetPiero MarchettiRomano RegazziPublished in: Nature communications (2020)
Fine-tuning of insulin release from pancreatic β-cells is essential to maintain blood glucose homeostasis. Here, we report that insulin secretion is regulated by a circular RNA containing the lariat sequence of the second intron of the insulin gene. Silencing of this intronic circular RNA in pancreatic islets leads to a decrease in the expression of key components of the secretory machinery of β-cells, resulting in impaired glucose- or KCl-induced insulin release and calcium signaling. The effect of the circular RNA is exerted at the transcriptional level and involves an interaction with the RNA-binding protein TAR DNA-binding protein 43 kDa (TDP-43). The level of this circularized intron is reduced in the islets of rodent diabetes models and of type 2 diabetic patients, possibly explaining their impaired secretory capacity. The study of this and other circular RNAs helps understanding β-cell dysfunction under diabetes conditions, and the etiology of this common metabolic disorder.
Keyphrases
- glycemic control
- blood glucose
- type diabetes
- binding protein
- induced apoptosis
- cell cycle arrest
- cardiovascular disease
- weight loss
- insulin resistance
- gene expression
- poor prognosis
- oxidative stress
- signaling pathway
- blood pressure
- endoplasmic reticulum stress
- copy number
- dna methylation
- left atrial appendage
- adipose tissue
- air pollution
- metabolic syndrome
- single molecule
- transcription factor
- single cell
- cell therapy
- heat stress
- atrial fibrillation
- skeletal muscle