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

Author:

Takemura Shin-ya1ORCID,Aso Yoshinori1ORCID,Hige Toshihide1,Wong Allan1,Lu Zhiyuan1,Xu C Shan1ORCID,Rivlin Patricia K1,Hess Harald1,Zhao Ting1,Parag Toufiq1,Berg Stuart1,Huang Gary1,Katz William1,Olbris Donald J1,Plaza Stephen1,Umayam Lowell1,Aniceto Roxanne1,Chang Lei-Ann1,Lauchie Shirley1,Ogundeyi Omotara1,Ordish Christopher1,Shinomiya Aya1,Sigmund Christopher1,Takemura Satoko1,Tran Julie1,Turner Glenn C1ORCID,Rubin Gerald M1ORCID,Scheffer Louis K1ORCID

Affiliation:

1. Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, United States

Abstract

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.

Funder

Howard Hughes Medical Institute

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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