Positive modulation of a Cys-loop acetylcholine receptor by an auxiliary transmembrane subunit

Nat Neurosci. 2012 Oct;15(10):1374-81. doi: 10.1038/nn.3197. Epub 2012 Aug 26.

Abstract

Auxiliary subunits regulate the trafficking, localization or gating kinetics of voltage- and ligand-gated ion channels by associating tightly and specifically with pore-forming subunits. However, no auxiliary subunits have been identified for members of the Cys-loop receptor superfamily. Here we identify MOLO-1, a positive regulator of levamisole-sensitive acetylcholine receptors (L-AChRs) at the Caenorhabditis elegans neuromuscular junction. MOLO-1 is a one-pass transmembrane protein that contains a single extracellular globular domain-the TPM domain, found in bacteria, plants and invertebrates, including nonvertebrate chordates. Loss of MOLO-1 impairs locomotion and renders worms resistant to the anthelmintic drug levamisole. In molo-1 mutants, L-AChR-dependent synaptic transmission is reduced by half, while the number and localization of receptors at synapses remain unchanged. In a heterologous expression system, MOLO-1 physically interacts with L-AChRs and directly enhances channel gating without affecting unitary conductance. The identification of MOLO-1 expands the mechanisms for generating functional and pharmacological diversity in the Cys-loop superfamily.

Publication types

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

MeSH terms

  • Animals
  • Caenorhabditis elegans
  • Caenorhabditis elegans Proteins / genetics
  • Caenorhabditis elegans Proteins / physiology*
  • Cholinergic Agonists / pharmacology
  • Cysteine Loop Ligand-Gated Ion Channel Receptors / agonists*
  • Cysteine Loop Ligand-Gated Ion Channel Receptors / genetics
  • Cysteine Loop Ligand-Gated Ion Channel Receptors / metabolism
  • Drug Resistance / genetics
  • Ion Channel Gating / drug effects
  • Ion Channel Gating / physiology
  • Ion Channels / genetics
  • Ion Channels / physiology*
  • Levamisole / pharmacology
  • Locomotion
  • Muscle Contraction / drug effects
  • Muscle Contraction / physiology
  • Mutation
  • Neuromuscular Junction / drug effects
  • Neuromuscular Junction / physiology
  • Protein Subunits / genetics
  • Protein Subunits / metabolism*
  • Receptors, Cholinergic / genetics
  • Receptors, Cholinergic / metabolism*
  • Synaptic Transmission / drug effects
  • Synaptic Transmission / physiology

Substances

  • Caenorhabditis elegans Proteins
  • Cholinergic Agonists
  • Cysteine Loop Ligand-Gated Ion Channel Receptors
  • Ion Channels
  • Protein Subunits
  • Receptors, Cholinergic
  • molo-1 protein, C elegans
  • Levamisole