PSD-95 binding dynamically regulates NLGN1 trafficking and function

Proc Natl Acad Sci U S A. 2019 Jun 11;116(24):12035-12044. doi: 10.1073/pnas.1821775116. Epub 2019 May 28.

Abstract

PSD-95 is a scaffolding protein that regulates the synaptic localization of many receptors, channels, and signaling proteins. The NLGN gene family encodes single-pass transmembrane postsynaptic cell adhesion molecules that are important for synapse assembly and function. At excitatory synapses, NLGN1 mediates transsynaptic binding with neurexin, a presynaptic cell adhesion molecule, and also binds to PSD-95, although the relevance of the PSD-95 interaction is not clear. We now show that disruption of the NLGN1 and PSD-95 interaction decreases surface expression of NLGN1 in cultured neurons. Furthermore, PKA phosphorylates NLGN1 on S839, near the PDZ ligand, and dynamically regulates PSD-95 binding. A phosphomimetic mutation of NLGN1 S839 significantly reduced PSD-95 binding. Impaired NLGN1/PSD-95 binding diminished synaptic NLGN1 expression and NLGN1-mediated synaptic enhancement. Our results establish a phosphorylation-dependent molecular mechanism that regulates NLGN1 and PSD-95 binding and provides insights into excitatory synaptic development and function.

Keywords: NLGN1; PKA; PSD-95; phosphorylation.

Publication types

  • Research Support, N.I.H., Intramural

MeSH terms

  • Animals
  • Cell Adhesion Molecules, Neuronal / metabolism*
  • Cells, Cultured
  • Disks Large Homolog 4 Protein / metabolism*
  • Female
  • HEK293 Cells
  • Humans
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Neuronal Plasticity / physiology
  • Neurons / metabolism
  • Phosphorylation / physiology
  • Protein Binding / physiology
  • Synapses / metabolism

Substances

  • Cell Adhesion Molecules, Neuronal
  • Disks Large Homolog 4 Protein
  • Dlg4 protein, mouse
  • neuroligin 1