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Sensorimotor Transformations in the Zebrafish Auditory System
Organisms use their sensory systems to acquire information from their environment and integrate this information to produce relevant behaviors. Nevertheless, how sensory information is converted into adequate motor patterns in the brain remains an open question. Here, we addressed this question usin...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6892253/ https://www.ncbi.nlm.nih.gov/pubmed/31708392 http://dx.doi.org/10.1016/j.cub.2019.10.020 |
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author | Privat, Martin Romano, Sebastián A. Pietri, Thomas Jouary, Adrien Boulanger-Weill, Jonathan Elbaz, Nicolas Duchemin, Auriane Soares, Daphne Sumbre, Germán |
author_facet | Privat, Martin Romano, Sebastián A. Pietri, Thomas Jouary, Adrien Boulanger-Weill, Jonathan Elbaz, Nicolas Duchemin, Auriane Soares, Daphne Sumbre, Germán |
author_sort | Privat, Martin |
collection | PubMed |
description | Organisms use their sensory systems to acquire information from their environment and integrate this information to produce relevant behaviors. Nevertheless, how sensory information is converted into adequate motor patterns in the brain remains an open question. Here, we addressed this question using two-photon and light-sheet calcium imaging in intact, behaving zebrafish larvae. We monitored neural activity elicited by auditory stimuli while simultaneously recording tail movements. We observed a spatial organization of neural activity according to four different response profiles (frequency tuning curves), suggesting a low-dimensional representation of frequency information, maintained throughout the development of the larvae. Low frequencies (150–450 Hz) were locally processed in the hindbrain and elicited motor behaviors. In contrast, higher frequencies (900–1,000 Hz) rarely induced motor behaviors and were also represented in the midbrain. Finally, we found that the sensorimotor transformations in the zebrafish auditory system are a continuous and gradual process that involves the temporal integration of the sensory response in order to generate a motor behavior. |
format | Online Article Text |
id | pubmed-6892253 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-68922532019-12-16 Sensorimotor Transformations in the Zebrafish Auditory System Privat, Martin Romano, Sebastián A. Pietri, Thomas Jouary, Adrien Boulanger-Weill, Jonathan Elbaz, Nicolas Duchemin, Auriane Soares, Daphne Sumbre, Germán Curr Biol Article Organisms use their sensory systems to acquire information from their environment and integrate this information to produce relevant behaviors. Nevertheless, how sensory information is converted into adequate motor patterns in the brain remains an open question. Here, we addressed this question using two-photon and light-sheet calcium imaging in intact, behaving zebrafish larvae. We monitored neural activity elicited by auditory stimuli while simultaneously recording tail movements. We observed a spatial organization of neural activity according to four different response profiles (frequency tuning curves), suggesting a low-dimensional representation of frequency information, maintained throughout the development of the larvae. Low frequencies (150–450 Hz) were locally processed in the hindbrain and elicited motor behaviors. In contrast, higher frequencies (900–1,000 Hz) rarely induced motor behaviors and were also represented in the midbrain. Finally, we found that the sensorimotor transformations in the zebrafish auditory system are a continuous and gradual process that involves the temporal integration of the sensory response in order to generate a motor behavior. Cell Press 2019-12-02 /pmc/articles/PMC6892253/ /pubmed/31708392 http://dx.doi.org/10.1016/j.cub.2019.10.020 Text en © 2019 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Privat, Martin Romano, Sebastián A. Pietri, Thomas Jouary, Adrien Boulanger-Weill, Jonathan Elbaz, Nicolas Duchemin, Auriane Soares, Daphne Sumbre, Germán Sensorimotor Transformations in the Zebrafish Auditory System |
title | Sensorimotor Transformations in the Zebrafish Auditory System |
title_full | Sensorimotor Transformations in the Zebrafish Auditory System |
title_fullStr | Sensorimotor Transformations in the Zebrafish Auditory System |
title_full_unstemmed | Sensorimotor Transformations in the Zebrafish Auditory System |
title_short | Sensorimotor Transformations in the Zebrafish Auditory System |
title_sort | sensorimotor transformations in the zebrafish auditory system |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6892253/ https://www.ncbi.nlm.nih.gov/pubmed/31708392 http://dx.doi.org/10.1016/j.cub.2019.10.020 |
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