CAPS1 RNA Editing Promotes Dense Core Vesicle Exocytosis

Cell Rep. 2016 Nov 15;17(8):2004-2014. doi: 10.1016/j.celrep.2016.10.073.

Abstract

Calcium-dependent activator protein for secretion 1 (CAPS1) plays a distinct role in the priming step of dense core vesicle (DCV) exocytosis. CAPS1 pre-mRNA is known to undergo adenosine-to-inosine RNA editing in its coding region, which results in a glutamate-to-glycine conversion at a site in its C-terminal region. However, the physiological significance of CAPS1 RNA editing remains elusive. Here, we created mutant mice in which edited CAPS1 was solely expressed. These mice were lean due to increased energy expenditure caused by physical hyperactivity. Electrophysiological and biochemical analyses demonstrated that the exocytosis of DCVs was upregulated in the chromaffin cells and neurons of these mice. Furthermore, we showed that edited CAPS1 bound preferentially to the activated form of syntaxin-1A, a component of the exocytotic fusion complex. These findings suggest that RNA editing regulates DCV exocytosis in vivo, affecting physical activity.

Keywords: ADAR; catecholamine; dense core vesicle; exocytosis; post-transcriptional modification; syntaxin-1A.

Publication types

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

MeSH terms

  • Adenosine Deaminase / metabolism
  • Animals
  • Biocatalysis
  • Body Weight
  • Calcium-Binding Proteins / genetics*
  • Calcium-Binding Proteins / metabolism
  • Catecholamines / metabolism
  • Energy Metabolism
  • Exocytosis*
  • Male
  • Mice
  • Mice, Mutant Strains
  • Nerve Tissue Proteins / genetics*
  • Nerve Tissue Proteins / metabolism
  • Nucleic Acid Conformation
  • PC12 Cells
  • Physical Conditioning, Animal
  • Protein Binding
  • RNA Editing / genetics*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • RNA-Binding Proteins / metabolism
  • Rats
  • Secretory Vesicles / metabolism*
  • Syntaxin 1 / metabolism

Substances

  • Cadps protein, mouse
  • Calcium-Binding Proteins
  • Catecholamines
  • Nerve Tissue Proteins
  • RNA, Messenger
  • RNA-Binding Proteins
  • Syntaxin 1
  • ADAR1 protein, mouse
  • ADAR2 protein, mouse
  • Adenosine Deaminase