Drosophila Choline transporter non-canonically regulates pupal eclosion and NMJ integrity through a neuronal subset of mushroom body

Dev Biol. 2019 Feb 1;446(1):80-93. doi: 10.1016/j.ydbio.2018.12.006. Epub 2018 Dec 7.

Abstract

Insect mushroom bodies (MB) have an ensemble of synaptic connections well-studied for their role in experience-dependent learning and several higher cognitive functions. MB requires neurotransmission for an efficient flow of information across synapses with different flexibility to meet the demand of the dynamically changing environment of an insect. Neurotransmitter transporters coordinate appropriate changes for an efficient neurotransmission at the synapse. Till date, there is no transporter reported for any of the previously known neurotransmitters in the intrinsic neurons of MB. In this study, we report a highly enriched expression of Choline Transporter (ChT) in Drosophila MB. We demonstrate that knockdown of ChT in a sub-type of MB neurons called α/β core (α/βc) and ϒ neurons leads to eclosion failure, peristaltic defect in larvae, and altered NMJ phenotype. These defects were neither observed on knockdown of proteins of the cholinergic locus in α/βc and ϒ neurons nor by knockdown of ChT in cholinergic neurons. Thus, our study provides insights into non-canonical roles of ChT in MB.

Keywords: Choline transporter; Drosophila; Eclosion; Mushroom body.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Animals, Genetically Modified
  • Cholinergic Neurons / metabolism
  • Drosophila Proteins / genetics
  • Drosophila Proteins / metabolism*
  • Drosophila melanogaster / genetics
  • Drosophila melanogaster / growth & development
  • Drosophila melanogaster / metabolism*
  • Gene Expression Regulation, Developmental
  • Larva / genetics
  • Larva / growth & development
  • Larva / metabolism
  • Membrane Transport Proteins / genetics
  • Membrane Transport Proteins / metabolism*
  • Mushroom Bodies / cytology
  • Mushroom Bodies / growth & development
  • Mushroom Bodies / metabolism*
  • Neuromuscular Junction / genetics
  • Neuromuscular Junction / growth & development
  • Neuromuscular Junction / metabolism*
  • Neurons / metabolism*
  • Pupa / genetics
  • Pupa / growth & development
  • Pupa / metabolism
  • RNA Interference
  • Synaptic Transmission / genetics
  • Synaptic Transmission / physiology

Substances

  • Drosophila Proteins
  • Membrane Transport Proteins
  • choline transporter