Neuropsychiatric disease-associated genetic variants of the dopamine transporter display heterogeneous molecular phenotypes

J Biol Chem. 2018 May 11;293(19):7250-7262. doi: 10.1074/jbc.RA118.001753. Epub 2018 Mar 20.

Abstract

Genetic factors are known to significantly contribute to the etiology of psychiatric diseases such as attention deficit hyperactivity disorder (ADHD) and autism spectrum and bipolar disorders, but the underlying molecular processes remain largely elusive. The dopamine transporter (DAT) has received continuous attention as a potential risk factor for psychiatric disease, as it is critical for dopamine homeostasis and serves as principal target for ADHD medications. Constrain metrics for the DAT-encoding gene, solute carrier family 6 member 3 (SLC6A3), indicate that missense mutations are under strong negative selection, pointing to pathophysiological outcomes when DAT function is compromised. Here, we systematically characterized six rare genetic variants of DAT (I312F, T356M, D421N, A559V, E602G, and R615C) identified in patients with neuropsychiatric disorders. We evaluated dopamine uptake and ligand interactions, along with ion coordination and electrophysiological properties, to elucidate functional phenotypes, and applied Zn2+ exposure and a substituted cysteine-accessibility approach to identify shared structural changes. Three variants (I312F, T356M, and D421N) exhibited impaired dopamine uptake associated with changes in ligand binding, ion coordination, and distinct conformational disturbances. Remarkably, we found that all three variants displayed gain-of-function electrophysiological phenotypes. I312F mediated an increased uncoupled anion conductance previously suggested to modulate neuronal excitability. T356M and D421N both mediated a cocaine-sensitive leakage of cations, which for T356M was potentiated by Zn2+, concurrent with partial functional rescue. Collectively, our findings support that gain of disruptive functions due to missense mutations in SLC6A3 may be key to understanding how dopaminergic dyshomeostasis arises in heterozygous carriers.

Keywords: attention-deficit hyperactivity disorder; autism; dopamine transporter; genetic polymorphism; missense mutation; molecular genetics; monoamine transporter; neurotransmitter transport; psychiatric disease; rare variants.

Publication types

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

MeSH terms

  • Animals
  • Attention Deficit Disorder with Hyperactivity / genetics*
  • Attention Deficit Disorder with Hyperactivity / physiopathology
  • Autism Spectrum Disorder / genetics*
  • Autism Spectrum Disorder / physiopathology
  • Bipolar Disorder / genetics*
  • Bipolar Disorder / physiopathology
  • COS Cells
  • Central Nervous System Stimulants / metabolism
  • Chlorocebus aethiops
  • Dopamine / metabolism
  • Dopamine Plasma Membrane Transport Proteins / chemistry
  • Dopamine Plasma Membrane Transport Proteins / genetics*
  • Dopamine Plasma Membrane Transport Proteins / metabolism
  • Gene Frequency
  • Genetic Markers
  • Genetic Variation*
  • Homeostasis
  • Humans
  • Ion Transport
  • Mutation, Missense
  • Patch-Clamp Techniques
  • Protein Binding
  • Protein Conformation
  • Zinc / metabolism

Substances

  • Central Nervous System Stimulants
  • Dopamine Plasma Membrane Transport Proteins
  • Genetic Markers
  • SLC6A3 protein, human
  • Zinc
  • Dopamine