TRIAD3/RNF216 mutations associated with Gordon Holmes syndrome lead to synaptic and cognitive impairments via Arc misregulation

Aging Cell. 2017 Apr;16(2):281-292. doi: 10.1111/acel.12551. Epub 2016 Dec 20.

Abstract

Multiple loss-of-function mutations in TRIAD3 (a.k.a. RNF216) have recently been identified in patients suffering from Gordon Holmes syndrome (GHS), characterized by cognitive decline, dementia, and movement disorders. TRIAD3A is an E3 ubiquitin ligase that recognizes and facilitates the ubiquitination of its target for degradation by the ubiquitin-proteasome system (UPS). Here, we demonstrate that two of these missense substitutions in TRIAD3 (R660C and R694C) could not regulate the degradation of their neuronal target, activity-regulated cytoskeletal-associated protein (Arc/Arg 3.1), whose expression is critical for synaptic plasticity and memory. The synaptic deficits due to the loss of endogenous TRIAD3A could not be rescued by TRIAD3A harboring GHS-associated missense mutations. Moreover, we demonstrate that the loss of endogenous TRIAD3A in the mouse hippocampal CA1 region led to deficits in spatial learning and memory. Finally, we show that these missense mutations abolished the interaction of TRIAD3A with Arc, disrupting Arc ubiquitination, and consequently Arc degradation. Our current findings of Arc misregulation by TRIAD3A variants suggest that loss-of-function mutations in TRIAD3A may contribute to dementia observed in patients with GHS driven by dysfunctional UPS components, leading to cognitive impairments through the synaptic protein Arc.

Keywords: Gordon Holmes syndrome; TRIAD3; activity-regulated cytoskeletal protein (Arc/Arg 3.1); behavior; dementia; learning and memory; synapse; ubiquitination.

Publication types

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

MeSH terms

  • Animals
  • CA1 Region, Hippocampal / pathology
  • Cerebellar Ataxia / genetics*
  • Clathrin / metabolism
  • Cognitive Dysfunction / metabolism
  • Cognitive Dysfunction / pathology*
  • Cytoskeletal Proteins / metabolism*
  • Endocytosis
  • Gene Knockdown Techniques
  • Gonadotropin-Releasing Hormone / deficiency*
  • Gonadotropin-Releasing Hormone / genetics
  • HEK293 Cells
  • Humans
  • Hypogonadism / genetics*
  • Mice, Inbred C57BL
  • Mutation / genetics*
  • Mutation, Missense / genetics
  • Nerve Tissue Proteins / metabolism*
  • Protein Binding
  • Proteolysis
  • Rats, Sprague-Dawley
  • Receptors, AMPA / metabolism
  • Spatial Memory
  • Synapses / metabolism
  • Synapses / pathology*
  • Synaptic Transmission
  • Ubiquitin-Protein Ligases / genetics*
  • Ubiquitin-Protein Ligases / metabolism
  • Ubiquitination

Substances

  • Clathrin
  • Cytoskeletal Proteins
  • Nerve Tissue Proteins
  • Receptors, AMPA
  • activity regulated cytoskeletal-associated protein
  • Gonadotropin-Releasing Hormone
  • RNF216 protein, mouse
  • Ubiquitin-Protein Ligases

Supplementary concepts

  • Cerebellar Ataxia and Hypogonadotropic Hypogonadism