Nicotinamide mononucleotide adenylyltransferase maintains active zone structure by stabilizing Bruchpilot

EMBO Rep. 2013 Jan;14(1):87-94. doi: 10.1038/embor.2012.181. Epub 2012 Nov 16.

Abstract

Active zones are specialized presynaptic structures critical for neurotransmission. We show that a neuronal maintenance factor, nicotinamide mononucleotide adenylyltransferase (NMNAT), is required for maintaining active zone structural integrity in Drosophila by interacting with the active zone protein, Bruchpilot (BRP), and shielding it from activity-induced ubiquitin-proteasome-mediated degradation. NMNAT localizes to the peri-active zone and interacts biochemically with BRP in an activity-dependent manner. Loss of NMNAT results in ubiquitination, mislocalization and aggregation of BRP, and subsequent active zone degeneration. We propose that, as a neuronal maintenance factor, NMNAT specifically maintains active zone structure by direct protein-protein interaction.

Publication types

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

MeSH terms

  • Animals
  • Drosophila / enzymology
  • Drosophila / genetics*
  • Drosophila Proteins / genetics*
  • Drosophila Proteins / metabolism
  • Gene Expression Regulation
  • Nicotinamide-Nucleotide Adenylyltransferase / antagonists & inhibitors
  • Nicotinamide-Nucleotide Adenylyltransferase / genetics*
  • Nicotinamide-Nucleotide Adenylyltransferase / metabolism
  • Presynaptic Terminals / enzymology*
  • Presynaptic Terminals / ultrastructure
  • Proteasome Endopeptidase Complex
  • Protein Binding
  • Proteolysis
  • RNA, Small Interfering / genetics
  • Signal Transduction
  • Synaptic Transmission / physiology
  • Ubiquitin / genetics
  • Ubiquitin / metabolism
  • Ubiquitination

Substances

  • BRP protein, Drosophila
  • Drosophila Proteins
  • RNA, Small Interfering
  • Ubiquitin
  • Nicotinamide-Nucleotide Adenylyltransferase
  • Proteasome Endopeptidase Complex