eLife (Jul 2017)

A connectome of a learning and memory center in the adult Drosophila brain

  • Shin-ya Takemura,
  • Yoshinori Aso,
  • Toshihide Hige,
  • Allan Wong,
  • Zhiyuan Lu,
  • C Shan Xu,
  • Patricia K Rivlin,
  • Harald Hess,
  • Ting Zhao,
  • Toufiq Parag,
  • Stuart Berg,
  • Gary Huang,
  • William Katz,
  • Donald J Olbris,
  • Stephen Plaza,
  • Lowell Umayam,
  • Roxanne Aniceto,
  • Lei-Ann Chang,
  • Shirley Lauchie,
  • Omotara Ogundeyi,
  • Christopher Ordish,
  • Aya Shinomiya,
  • Christopher Sigmund,
  • Satoko Takemura,
  • Julie Tran,
  • Glenn C Turner,
  • Gerald M Rubin,
  • Louis K Scheffer

DOI
https://doi.org/10.7554/eLife.26975
Journal volume & issue
Vol. 6

Abstract

Read online

Understanding memory formation, storage and retrieval requires knowledge of the underlying neuronal circuits. In Drosophila, the mushroom body (MB) is the major site of associative learning. We reconstructed the morphologies and synaptic connections of all 983 neurons within the three functional units, or compartments, that compose the adult MB’s α lobe, using a dataset of isotropic 8 nm voxels collected by focused ion-beam milling scanning electron microscopy. We found that Kenyon cells (KCs), whose sparse activity encodes sensory information, each make multiple en passant synapses to MB output neurons (MBONs) in each compartment. Some MBONs have inputs from all KCs, while others differentially sample sensory modalities. Only 6% of KC>MBON synapses receive a direct synapse from a dopaminergic neuron (DAN). We identified two unanticipated classes of synapses, KC>DAN and DAN>MBON. DAN activation produces a slow depolarization of the MBON in these DAN>MBON synapses and can weaken memory recall.

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