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Mechanosensory input during circuit formation shapes Drosophila motor behavior through Patterned Spontaneous Network Activity

View ORCID ProfileArnaldo Carreira-Rosario, Ryan A. York, Minseung Choi, Chris Q. Doe, Thomas R. Clandinin
doi: https://doi.org/10.1101/2021.03.21.436277
Arnaldo Carreira-Rosario
1Department of Neurobiology, Stanford University, Stanford, CA 94305
2Institute of Neuroscience, Howard Hughes Medical Institute, University of Oregon, Eugene, OR 97403
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  • ORCID record for Arnaldo Carreira-Rosario
Ryan A. York
1Department of Neurobiology, Stanford University, Stanford, CA 94305
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Minseung Choi
1Department of Neurobiology, Stanford University, Stanford, CA 94305
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Chris Q. Doe
2Institute of Neuroscience, Howard Hughes Medical Institute, University of Oregon, Eugene, OR 97403
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  • For correspondence: trc@stanford.edu cdoe@uoregon.edu
Thomas R. Clandinin
1Department of Neurobiology, Stanford University, Stanford, CA 94305
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  • For correspondence: trc@stanford.edu cdoe@uoregon.edu
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Summary

Neural activity sculpts circuit wiring in many animals. In vertebrates, patterned spontaneous network activity (PaSNA) generates sensory maps and establishes local circuits 1–3. However, it remains unclear how PaSNA might shape neuronal circuits and behavior in invertebrates. Previous work in the developing Drosophila embryo discovered spontaneous muscle activity that did not require synaptic transmission, and hence was myogenic, preceding PaSNA 4–6. These studies, however, monitored muscle movement, not neural activity, and were therefore unable to observe how myogenic activity might relate to subsequent neural network engagement. Here we use calcium imaging to directly record neural activity and characterize the emergence of PaSNA. We demonstrate that the spatiotemporal properties of PaSNA are highly stereotyped across embryos, arguing for genetic programming. Consistent with previous observations, we observe neural activity well before it becomes patterned, initially emerging during the myogenic stage. Remarkably, inhibition of mechanosensory input as well as inhibition of muscle contractions results in premature and excessive PaSNA, demonstrating that muscle movement serves as a brake on this process. Finally, using an optogenetic strategy to selectively disrupt mechanosensory inputs during PaSNA, followed by quantitative modeling of larval behavior, we demonstrate that mechanosensory modulation during development is required for proper larval foraging. This work thus provides a foundation for using the Drosophila embryo to study the role of PaSNA in circuit formation, provides mechanistic insight into how PaSNA is entrained by motor activity, and demonstrates that spontaneous network activity is essential for locomotor behavior. These studies argue that sensory feedback during the earliest stages of circuit formation can sculpt locomotor behaviors through innate motor learning.

Highlights

  • PaSNA in the Drosophila embryonic CNS is spatiotemporally stereotyped

  • Mechanosensory neurons negatively modulate PaSNA

  • Embryonic PaSNA is required for larval locomotor behavior

Competing Interest Statement

The authors have declared no competing interest.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC 4.0 International license.
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Posted July 09, 2021.
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Mechanosensory input during circuit formation shapes Drosophila motor behavior through Patterned Spontaneous Network Activity
Arnaldo Carreira-Rosario, Ryan A. York, Minseung Choi, Chris Q. Doe, Thomas R. Clandinin
bioRxiv 2021.03.21.436277; doi: https://doi.org/10.1101/2021.03.21.436277
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Mechanosensory input during circuit formation shapes Drosophila motor behavior through Patterned Spontaneous Network Activity
Arnaldo Carreira-Rosario, Ryan A. York, Minseung Choi, Chris Q. Doe, Thomas R. Clandinin
bioRxiv 2021.03.21.436277; doi: https://doi.org/10.1101/2021.03.21.436277

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