A role for alternative splicing in circadian control of exocytosis and glucose homeostasis

Genes Dev. 2020 Aug 1;34(15-16):1089-1105. doi: 10.1101/gad.338178.120. Epub 2020 Jul 2.

Abstract

The circadian clock is encoded by a negative transcriptional feedback loop that coordinates physiology and behavior through molecular programs that remain incompletely understood. Here, we reveal rhythmic genome-wide alternative splicing (AS) of pre-mRNAs encoding regulators of peptidergic secretion within pancreatic β cells that are perturbed in Clock-/- and Bmal1-/- β-cell lines. We show that the RNA-binding protein THRAP3 (thyroid hormone receptor-associated protein 3) regulates circadian clock-dependent AS by binding to exons at coding sequences flanking exons that are more frequently skipped in clock mutant β cells, including transcripts encoding Cask (calcium/calmodulin-dependent serine protein kinase) and Madd (MAP kinase-activating death domain). Depletion of THRAP3 restores expression of the long isoforms of Cask and Madd, and mimicking exon skipping in these transcripts through antisense oligonucleotide delivery in wild-type islets reduces glucose-stimulated insulin secretion. Finally, we identify shared networks of alternatively spliced exocytic genes from islets of rodent models of diet-induced obesity that significantly overlap with clock mutants. Our results establish a role for pre-mRNA alternative splicing in β-cell function across the sleep/wake cycle.

Keywords: CASK; MADD; RNA sequencing; SNAP25; THRAP3; alternative splicing; circadian clock; exocytosis; insulin secretion; transcriptomics.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • ARNTL Transcription Factors / genetics
  • ARNTL Transcription Factors / physiology
  • Alternative Splicing*
  • Animals
  • CLOCK Proteins / genetics
  • CLOCK Proteins / physiology
  • Cells, Cultured
  • Circadian Clocks / genetics*
  • Death Domain Receptor Signaling Adaptor Proteins / genetics
  • Death Domain Receptor Signaling Adaptor Proteins / metabolism
  • Exocytosis*
  • Glucose / metabolism*
  • Guanine Nucleotide Exchange Factors / genetics
  • Guanine Nucleotide Exchange Factors / metabolism
  • Guanylate Kinases / genetics
  • Guanylate Kinases / metabolism
  • Homeostasis
  • Insulin Secretion / genetics*
  • Insulin-Secreting Cells / metabolism
  • Islets of Langerhans / metabolism
  • Male
  • Mice, Inbred C57BL
  • Nuclear Proteins / physiology
  • Obesity / genetics
  • Obesity / metabolism
  • Synaptosomal-Associated Protein 25 / genetics
  • Synaptosomal-Associated Protein 25 / metabolism
  • Transcription Factors / physiology

Substances

  • ARNTL Transcription Factors
  • Bmal1 protein, mouse
  • Death Domain Receptor Signaling Adaptor Proteins
  • Guanine Nucleotide Exchange Factors
  • Madd protein, mouse
  • Nuclear Proteins
  • Snap25 protein, mouse
  • Synaptosomal-Associated Protein 25
  • Thrap3 protein, mouse
  • Transcription Factors
  • CLOCK Proteins
  • Clock protein, mouse
  • CASK kinases
  • Guanylate Kinases
  • Glucose