Transcriptional regulation of the miR-212/miR-132 cluster in insulin-secreting β-cells by cAMP-regulated transcriptional co-activator 1 and salt-inducible kinases

Mol Cell Endocrinol. 2016 Mar 15:424:23-33. doi: 10.1016/j.mce.2016.01.010. Epub 2016 Jan 13.

Abstract

MicroRNAs are central players in the control of insulin secretion, but their transcriptional regulation is poorly understood. Our aim was to investigate cAMP-mediated transcriptional regulation of the miR-212/miR-132 cluster and involvement of further upstream proteins in insulin secreting β-cells. cAMP induced by forskolin+IBMX or GLP-1 caused increased expression of miR-212/miR-132, and elevated phosphorylation of cAMP-response-element-binding-protein (CREB)/Activating-transcription-factor-1 (ATF1) and Salt-Inducible-Kinases (SIKs). CyclicAMP-Regulated Transcriptional Co-activator-1 (CRTC1) was concomitantly dephosphorylated and translocated to the nucleus. Silencing of miR-212/miR-132 reduced, and overexpression of miR-212 increased, glucose-stimulated insulin secretion. Silencing of CRTC1 expression resulted in decreased insulin secretion and miR-212/miR-132 expression, while silencing or inhibition of SIKs was associated with increased expression of the microRNAs and dephosphorylation of CRTC1. CRTC1 protein levels were reduced after silencing of miR-132, suggesting feed-back regulation. Our data propose cAMP-dependent co-regulation of miR-212/miR-132, in part mediated through SIK-regulated CRTC1, as an important factor for fine-tuned regulation of insulin secretion.

Keywords: Beta cell; Diabetes; Insulin secretion; Transcription; cAMP; microRNA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Female
  • Gene Expression Regulation / drug effects
  • Glucose / pharmacology*
  • Humans
  • Insulin-Secreting Cells / cytology
  • Insulin-Secreting Cells / drug effects
  • Insulin-Secreting Cells / metabolism*
  • Male
  • MicroRNAs / genetics*
  • Middle Aged
  • Phosphorylation / drug effects
  • Protein Serine-Threonine Kinases / metabolism*
  • Rats
  • Rats, Wistar
  • Transcription Factors / metabolism*
  • Transcription, Genetic*

Substances

  • Crtc1 protein, rat
  • MIRN132 microRNA, rat
  • MIRN212 microRNA, rat
  • MicroRNAs
  • Transcription Factors
  • Protein Serine-Threonine Kinases
  • Glucose