Published December 19, 2018 | Version Accepted Version + Supplemental Material
Journal Article Open

A Brain Module for Scalable Control of Complex, Multi-motor Threat Displays

  • 1. ROR icon California Institute of Technology
  • 2. ROR icon Howard Hughes Medical Institute

Abstract

Threat displays are a universal feature of agonistic interactions. Whether threats are part of a continuum of aggressive behaviors or separately controlled remains unclear. We analyze threats in Drosophila and show they are triggered by male cues and visual motion, and comprised of multiple motor elements that can be flexibly combined. We isolate a cluster of ∼3 neurons whose activity is necessary for threat displays but not for other aggressive behaviors, and whose artificial activation suffices to evoke naturalistic threats in solitary flies, suggesting that the neural control of threats is modular with respect to other aggressive behaviors. Artificially evoked threats suffice to repel opponents from a resource in the absence of contact aggression. Depending on its level of artificial activation, this neural threat module can evoke different motor elements in a threshold-dependent manner. Such scalable modules may represent fundamental "building blocks" of neural circuits that mediate complex multi-motor behaviors.

Additional Information

© 2018 Elsevier Inc. Received 19 May 2018, Revised 11 September 2018, Accepted 16 October 2018, Available online 8 November 2018. We thank Gerry Rubin for sharing unpublished reagents (see Key Resources Table); Talmo Pereira for classification code; Kiichi Watanabe for performing the experiments in Figure S7E; Hidehiko Inagaki for sharing R21B10-FLP; Jon Schor, Ruohan Wang, Alberto Corona, Michael Altermatt, and Jared Everson (students) and Yonil Jung, Peter Weir, Michael Dickinson, Mhemet Keles, and Mark Frye for help with Ca^(2+) imaging experiments; Kavya Sreedhar, Luciana Hartmann, Romann Webber, and Yisong Yue for assistance with transition diagrams; Evan Tanner for SV1 code; Ana Silbering and Richard Benton for quad olfactory mutants; Barry Dickson for FruM anti-body; and Anderson lab members who provided expertise and comments. B.J.D. was a Life Sciences Research Foundation fellow for the Ellison Medical Foundation. D.J.A. is an Investigator of the Howard Hughes Medical Institute and supported by NIH grant #DA031389. Author Contributions: D.J.A. and B.J.D. conceived the project, designed experiments and interpreted the results. B.J.D. conducted experiments, made figures, and with D.J.A. co-wrote the manuscript. B.D.P. provided reagents and expertise. E.H. originally identified and provided advanced access to R20E08 and Split Gal4s. The authors declare no competing interests.

Attached Files

Accepted Version - nihms-1511838.pdf

Supplemental Material - 1-s2.0-S0896627318309358-mmc1.pdf

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Additional details

Identifiers

PMCID
PMC6314657
Eprint ID
90755
Resolver ID
CaltechAUTHORS:20181108-124509340

Funding

Ellison Medical Foundation
Howard Hughes Medical Institute (HHMI)
NIH
DA031389

Dates

Created
2018-11-08
Created from EPrint's datestamp field
Updated
2022-02-16
Created from EPrint's last_modified field