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Midbrain node for context-specific vocalisation in fish

Author

Listed:
  • Eric R. Schuppe

    (Cornell University
    University of California San Francisco School of Medicine)

  • Irene Ballagh

    (Cornell University
    The University of British Columbia)

  • Najva Akbari

    (Cornell University
    Stanford University)

  • Wenxuan Fang

    (Cornell University
    The University of British Columbia)

  • Jonathan T. Perelmuter

    (Cornell University)

  • Caleb H. Radtke

    (Cornell University)

  • Margaret A. Marchaterre

    (Cornell University)

  • Andrew H. Bass

    (Cornell University)

Abstract

Vocalizations communicate information indicative of behavioural state across divergent social contexts. Yet, how brain regions actively pattern the acoustic features of context-specific vocal signals remains largely unexplored. The midbrain periaqueductal gray (PAG) is a major site for initiating vocalization among mammals, including primates. We show that PAG neurons in a highly vocal fish species (Porichthys notatus) are activated in distinct patterns during agonistic versus courtship calling by males, with few co-activated during a non-vocal behaviour, foraging. Pharmacological manipulations within vocally active PAG, but not hindbrain, sites evoke vocal network output to sonic muscles matching the temporal features of courtship and agonistic calls, showing that a balance of inhibitory and excitatory dynamics is likely necessary for patterning different call types. Collectively, these findings support the hypothesis that vocal species of fish and mammals share functionally comparable PAG nodes that in some species can influence the acoustic structure of social context-specific vocal signals.

Suggested Citation

  • Eric R. Schuppe & Irene Ballagh & Najva Akbari & Wenxuan Fang & Jonathan T. Perelmuter & Caleb H. Radtke & Margaret A. Marchaterre & Andrew H. Bass, 2024. "Midbrain node for context-specific vocalisation in fish," Nature Communications, Nature, vol. 15(1), pages 1-16, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-023-43794-y
    DOI: 10.1038/s41467-023-43794-y
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    References listed on IDEAS

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    1. Zheng Wu & Anita E. Autry & Joseph F. Bergan & Mitsuko Watabe-Uchida & Catherine G. Dulac, 2014. "Galanin neurons in the medial preoptic area govern parental behaviour," Nature, Nature, vol. 509(7500), pages 325-330, May.
    2. Jingyi Chen & Jeffrey E. Markowitz & Varoth Lilascharoen & Sandra Taylor & Pete Sheurpukdi & Jason A. Keller & Jennifer R. Jensen & Byung Kook Lim & Sandeep Robert Datta & Lisa Stowers, 2021. "Flexible scaling and persistence of social vocal communication," Nature, Nature, vol. 593(7857), pages 108-113, May.
    3. Boris P. Chagnaud & Robert Baker & Andrew H. Bass, 2011. "Vocalization frequency and duration are coded in separate hindbrain nuclei," Nature Communications, Nature, vol. 2(1), pages 1-11, September.
    4. Gabriel Jorgewich-Cohen & Simon William Townsend & Linilson Rodrigues Padovese & Nicole Klein & Peter Praschag & Camila R. Ferrara & Stephan Ettmar & Sabrina Menezes & Arthur Pinatti Varani & Jaren Se, 2022. "Common evolutionary origin of acoustic communication in choanate vertebrates," Nature Communications, Nature, vol. 13(1), pages 1-7, December.
    5. Zhuo Chen & John J. Wiens, 2020. "The origins of acoustic communication in vertebrates," Nature Communications, Nature, vol. 11(1), pages 1-8, December.
    6. Dayu Lin & Maureen P. Boyle & Piotr Dollar & Hyosang Lee & E. S. Lein & Pietro Perona & David J. Anderson, 2011. "Functional identification of an aggression locus in the mouse hypothalamus," Nature, Nature, vol. 470(7333), pages 221-226, February.
    7. James L. Goodson & Andrew H. Bass, 2000. "Forebrain peptides modulate sexually polymorphic vocal circuitry," Nature, Nature, vol. 403(6771), pages 769-772, February.
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