@article {48658, title = {A connectome of a learning and memory center in the adult Drosophila brain.}, journal = {eLife}, volume = {6}, year = {2017}, month = {2017 Jul 18}, pages = {e26975}, 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{\textquoteright}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 six percent 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.

}, doi = {10.7554/eLife.26975}, author = {Takemura, Shin-ya and Aso, Yoshinori and Hige, Toshihide and Wong, Allan M and Lu, Zhiyuan and Xu, C Shan and Rivlin, Patricia K and Hess, Harald F and Zhao, Ting and Parag, Toufiq and Berg, Stuart and Huang, Gary and Katz, William T and Olbris, Donald J and Plaza, Stephen M and Umayam, Lowell A and Aniceto, Roxanne and Chang, Lei-Ann and Lauchie, Shirley and et al} } @article {48646, title = {Mapping the neural substrates of behavior.}, journal = {Cell}, volume = {170}, year = {2017}, month = {2017-07-13}, pages = {393-406}, abstract = {

Assigning behavioral functions to neural structures has long been a central goal in neuroscience and is a necessary first step toward a circuit-level understanding of how the brain generates behavior. Here, we map the neural substrates of locomotion and social behaviors for Drosophila melanogaster using automated machine-vision and machine-learning techniques. From videos of 400,000 flies, we quantified the behavioral effects of activating 2,204 genetically targeted populations of neurons. We combined a novel quantification of anatomy with our behavioral analysis to create brain-behavior correlation maps, which are shared as browsable web pages and interactive software. Based on these maps, we generated hypotheses of regions of the brain causally related to sensory processing, locomotor control, courtship, aggression, and sleep. Our maps directly specify genetic tools to target these regions, which we used to identify a small population of neurons with a role in the control of walking.

{\textbullet}We developed machine-vision methods to broadly and precisely quantify fly behavior{\textbullet}We measured effects of activating 2,204 genetically targeted neuronal populations{\textbullet}We created whole-brain maps of neural substrates of locomotor and social behaviors{\textbullet}We created resources for exploring our results and enabling further investigation

Machine-vision analyses of large behavior and neuroanatomy data reveal whole-brain maps of regions associated with numerous complex behaviors.

}, doi = {10.1016/j.cell.2017.06.032}, url = {http://dx.doi.org/10.1016/j.cell.2017.06.032}, author = {Robie, Alice A and Hirokawa, Jonathan and Edwards, Austin W and Umayam, Lowell A and Lee, Allen and Phillips, Mary L and Card, Gwyneth M and Korff, Wyatt and Rubin, Gerald M and Simpson, Julie H and Reiser, Michael B and Branson, Kristin M} }