Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Privat, Martin, Romano, Sebastián A., Pietri, Thomas, Jouary, Adrien, Boulanger-Weill, Jonathan, Elbaz, Nicolas, Duchemin, Auriane, Soares, Daphne, Sumbre, Germán
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2019
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
_version_ 1783475994794917888
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
work_keys_str_mv AT privatmartin sensorimotortransformationsinthezebrafishauditorysystem
AT romanosebastiana sensorimotortransformationsinthezebrafishauditorysystem
AT pietrithomas sensorimotortransformationsinthezebrafishauditorysystem
AT jouaryadrien sensorimotortransformationsinthezebrafishauditorysystem
AT boulangerweilljonathan sensorimotortransformationsinthezebrafishauditorysystem
AT elbaznicolas sensorimotortransformationsinthezebrafishauditorysystem
AT ducheminauriane sensorimotortransformationsinthezebrafishauditorysystem
AT soaresdaphne sensorimotortransformationsinthezebrafishauditorysystem
AT sumbregerman sensorimotortransformationsinthezebrafishauditorysystem