TY - JOUR
T1 - A Drosophila computational brain model reveals sensorimotor processing
AU - Shiu, Philip K.
AU - Sterne, Gabriella R.
AU - Spiller, Nico
AU - Franconville, Romain
AU - Sandoval, Andrea
AU - Zhou, Joie
AU - Simha, Neha
AU - Kang, Chan Hyuk
AU - Yu, Seongbong
AU - Kim, Jinseop S.
AU - Dorkenwald, Sven
AU - Matsliah, Arie
AU - Schlegel, Philipp
AU - Yu, Szi Chieh
AU - McKellar, Claire E.
AU - Sterling, Amy
AU - Costa, Marta
AU - Eichler, Katharina
AU - Bates, Alexander Shakeel
AU - Eckstein, Nils
AU - Funke, Jan
AU - Jefferis, Gregory S.X.E.
AU - Murthy, Mala
AU - Bidaye, Salil S.
AU - Hampel, Stefanie
AU - Seeds, Andrew M.
AU - Scott, Kristin
N1 - Publisher Copyright:
© The Author(s) 2024.
PY - 2024/10/3
Y1 - 2024/10/3
N2 - The recent assembly of the adult Drosophila melanogaster central brain connectome, containing more than 125,000 neurons and 50 million synaptic connections, provides a template for examining sensory processing throughout the brain1,2. Here we create a leaky integrate-and-fire computational model of the entire Drosophila brain, on the basis of neural connectivity and neurotransmitter identity3, to study circuit properties of feeding and grooming behaviours. We show that activation of sugar-sensing or water-sensing gustatory neurons in the computational model accurately predicts neurons that respond to tastes and are required for feeding initiation4. In addition, using the model to activate neurons in the feeding region of the Drosophila brain predicts those that elicit motor neuron firing5—a testable hypothesis that we validate by optogenetic activation and behavioural studies. Activating different classes of gustatory neurons in the model makes accurate predictions of how several taste modalities interact, providing circuit-level insight into aversive and appetitive taste processing. Additionally, we applied this model to mechanosensory circuits and found that computational activation of mechanosensory neurons predicts activation of a small set of neurons comprising the antennal grooming circuit, and accurately describes the circuit response upon activation of different mechanosensory subtypes6–10. Our results demonstrate that modelling brain circuits using only synapse-level connectivity and predicted neurotransmitter identity generates experimentally testable hypotheses and can describe complete sensorimotor transformations.
AB - The recent assembly of the adult Drosophila melanogaster central brain connectome, containing more than 125,000 neurons and 50 million synaptic connections, provides a template for examining sensory processing throughout the brain1,2. Here we create a leaky integrate-and-fire computational model of the entire Drosophila brain, on the basis of neural connectivity and neurotransmitter identity3, to study circuit properties of feeding and grooming behaviours. We show that activation of sugar-sensing or water-sensing gustatory neurons in the computational model accurately predicts neurons that respond to tastes and are required for feeding initiation4. In addition, using the model to activate neurons in the feeding region of the Drosophila brain predicts those that elicit motor neuron firing5—a testable hypothesis that we validate by optogenetic activation and behavioural studies. Activating different classes of gustatory neurons in the model makes accurate predictions of how several taste modalities interact, providing circuit-level insight into aversive and appetitive taste processing. Additionally, we applied this model to mechanosensory circuits and found that computational activation of mechanosensory neurons predicts activation of a small set of neurons comprising the antennal grooming circuit, and accurately describes the circuit response upon activation of different mechanosensory subtypes6–10. Our results demonstrate that modelling brain circuits using only synapse-level connectivity and predicted neurotransmitter identity generates experimentally testable hypotheses and can describe complete sensorimotor transformations.
UR - https://www.scopus.com/pages/publications/85205528034
U2 - 10.1038/s41586-024-07763-9
DO - 10.1038/s41586-024-07763-9
M3 - Article
C2 - 39358519
AN - SCOPUS:85205528034
SN - 0028-0836
VL - 634
SP - 210
EP - 219
JO - Nature
JF - Nature
IS - 8032
ER -