ArticleNature communications2025
A neural circuit for context-dependent multimodal signaling in Drosophila.
Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
4 citing papers in PubMed.
- Sex-specific behavioral feedback modulates sensorimotor processing and drives flexible social behavior.Nature communications · 2026Article
- Sequencing of distinct wing behaviors during Drosophila courtship.Current biology : CB · 2026Article
- Neural evolution of complex motor behaviors: insights from Drosophila courtship song.Current opinion in neurobiology · 2025Review
- Sequencing of distinct wing behaviors duringbioRxiv : the preprint server for biology · 2025Article
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Authors and funding
7 authors.
Funding
Abstract
Many animals produce multimodal displays that combine acoustic, visual, or vibratory signals, yet the neural mechanisms coordinating these behaviors remain unclear. Using Drosophila courtship as a model, we reveal how a single neural circuit integrates sensory cues and motivational state to orchestrate multimodal signaling. Male flies produce both air-borne song and substrate-borne vibrations during courtship, but in distinct, largely non-overlapping contexts. We demonstrate that the same brain neurons that drive song also control vibrations through separate pre-motor pathways, with cell-type specific dynamics. This shared circuit coordinates multimodal displays with locomotion, ensuring vibrations are produced only when they can effectively reach the female. The circuit employs shared motifs-recurrence and mutual inhibition-that enable dynamic control of multimodal signals by external cues and internal state. A computational model confirms that these motifs are sufficient to explain the observed behavioral dynamics. Our findings illustrate how simple neural circuit elements can be combined to select and coordinate complex multimodal behaviors.
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