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Behavioral analysis through the lifespan of disc1 mutant zebrafish identifies defects in sensorimotor transformation
DISC1 is a genetic risk factor for multiple psychiatric disorders. Compared to the dozens of murine Disc1 models, there is a paucity of zebrafish disc1 models—an organism amenable to high-throughput experimentation. We conducted the longitudinal neurobehavioral analysis of disc1 mutant zebrafish acr...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10320522/ https://www.ncbi.nlm.nih.gov/pubmed/37416451 http://dx.doi.org/10.1016/j.isci.2023.107099 |
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author | Pluimer, Brock R. Harrison, Devin L. Boonyavairoje, Chanon Prinssen, Eric P. Rogers-Evans, Mark Peterson, Randall T. Thyme, Summer B. Nath, Anjali K. |
author_facet | Pluimer, Brock R. Harrison, Devin L. Boonyavairoje, Chanon Prinssen, Eric P. Rogers-Evans, Mark Peterson, Randall T. Thyme, Summer B. Nath, Anjali K. |
author_sort | Pluimer, Brock R. |
collection | PubMed |
description | DISC1 is a genetic risk factor for multiple psychiatric disorders. Compared to the dozens of murine Disc1 models, there is a paucity of zebrafish disc1 models—an organism amenable to high-throughput experimentation. We conducted the longitudinal neurobehavioral analysis of disc1 mutant zebrafish across key stages of life. During early developmental stages, disc1 mutants exhibited abrogated behavioral responses to sensory stimuli across multiple testing platforms. Moreover, during exposure to an acoustic sensory stimulus, loss of disc1 resulted in the abnormal activation of neurons in the pallium, cerebellum, and tectum—anatomical sites involved in the integration of sensory perception and motor control. In adulthood, disc1 mutants exhibited sexually dimorphic reduction in anxiogenic behavior in novel paradigms. Together, these findings implicate disc1 in sensorimotor processes and the genesis of anxiogenic behaviors, which could be exploited for the development of novel treatments in addition to investigating the biology of sensorimotor transformation in the context of disc1 deletion. |
format | Online Article Text |
id | pubmed-10320522 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-103205222023-07-06 Behavioral analysis through the lifespan of disc1 mutant zebrafish identifies defects in sensorimotor transformation Pluimer, Brock R. Harrison, Devin L. Boonyavairoje, Chanon Prinssen, Eric P. Rogers-Evans, Mark Peterson, Randall T. Thyme, Summer B. Nath, Anjali K. iScience Article DISC1 is a genetic risk factor for multiple psychiatric disorders. Compared to the dozens of murine Disc1 models, there is a paucity of zebrafish disc1 models—an organism amenable to high-throughput experimentation. We conducted the longitudinal neurobehavioral analysis of disc1 mutant zebrafish across key stages of life. During early developmental stages, disc1 mutants exhibited abrogated behavioral responses to sensory stimuli across multiple testing platforms. Moreover, during exposure to an acoustic sensory stimulus, loss of disc1 resulted in the abnormal activation of neurons in the pallium, cerebellum, and tectum—anatomical sites involved in the integration of sensory perception and motor control. In adulthood, disc1 mutants exhibited sexually dimorphic reduction in anxiogenic behavior in novel paradigms. Together, these findings implicate disc1 in sensorimotor processes and the genesis of anxiogenic behaviors, which could be exploited for the development of novel treatments in addition to investigating the biology of sensorimotor transformation in the context of disc1 deletion. Elsevier 2023-06-14 /pmc/articles/PMC10320522/ /pubmed/37416451 http://dx.doi.org/10.1016/j.isci.2023.107099 Text en © 2023 The Author(s) https://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 Pluimer, Brock R. Harrison, Devin L. Boonyavairoje, Chanon Prinssen, Eric P. Rogers-Evans, Mark Peterson, Randall T. Thyme, Summer B. Nath, Anjali K. Behavioral analysis through the lifespan of disc1 mutant zebrafish identifies defects in sensorimotor transformation |
title | Behavioral analysis through the lifespan of disc1 mutant zebrafish identifies defects in sensorimotor transformation |
title_full | Behavioral analysis through the lifespan of disc1 mutant zebrafish identifies defects in sensorimotor transformation |
title_fullStr | Behavioral analysis through the lifespan of disc1 mutant zebrafish identifies defects in sensorimotor transformation |
title_full_unstemmed | Behavioral analysis through the lifespan of disc1 mutant zebrafish identifies defects in sensorimotor transformation |
title_short | Behavioral analysis through the lifespan of disc1 mutant zebrafish identifies defects in sensorimotor transformation |
title_sort | behavioral analysis through the lifespan of disc1 mutant zebrafish identifies defects in sensorimotor transformation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10320522/ https://www.ncbi.nlm.nih.gov/pubmed/37416451 http://dx.doi.org/10.1016/j.isci.2023.107099 |
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