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Modeling Neuronal Diseases in Zebrafish in the Era of CRISPR
BACKGROUND: Danio rerio is a powerful experimental model for studies in genetics and development. Recently, CRISPR technology has been applied in this species to mimic various human diseases, including those affecting the nervous system. Zebrafish offer multiple experimental advantages: external emb...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Bentham Science Publishers
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7324878/ https://www.ncbi.nlm.nih.gov/pubmed/31573887 http://dx.doi.org/10.2174/1570159X17666191001145550 |
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author | Espino-Saldaña, Angeles Edith Rodríguez-Ortiz, Roberto Pereida-Jaramillo, Elizabeth Martínez-Torres, Ataúlfo |
author_facet | Espino-Saldaña, Angeles Edith Rodríguez-Ortiz, Roberto Pereida-Jaramillo, Elizabeth Martínez-Torres, Ataúlfo |
author_sort | Espino-Saldaña, Angeles Edith |
collection | PubMed |
description | BACKGROUND: Danio rerio is a powerful experimental model for studies in genetics and development. Recently, CRISPR technology has been applied in this species to mimic various human diseases, including those affecting the nervous system. Zebrafish offer multiple experimental advantages: external embryogenesis, rapid development, transparent embryos, short life cycle, and basic neurobiological processes shared with humans. This animal model, together with the CRISPR system and, emerging imaging technologies, and novel behavioral approaches, lay the basis for a prominent future in neuropathology and will undoubtedly accelerate our understanding of brain function and its disorders. OBJECTIVE: Gather relevant findings from studies that have used CRISPR technologies in zebrafish to explore basic neuronal function and model human diseases. METHODS: We systematically reviewed the most recent literature about CRISPR technology applications for understanding brain function and neurological disorders in D. rerio. We highlighted the key role of CRISPR in driving forward our understanding of particular topics in neuroscience. RESULTS: We show specific advances in neurobiology when the CRISPR system has been applied in zebrafish and describe how CRISPR is accelerating our understanding of brain organization. CONCLUSION: Today, CRISPR is the preferred method to modify genomes of practically any living organism. Despite the rapid development of CRISPR technologies to generate disease models in zebrafish, more efforts are needed to efficiently combine different disciplines to find the etiology and treatments for many brain diseases. |
format | Online Article Text |
id | pubmed-7324878 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Bentham Science Publishers |
record_format | MEDLINE/PubMed |
spelling | pubmed-73248782020-08-01 Modeling Neuronal Diseases in Zebrafish in the Era of CRISPR Espino-Saldaña, Angeles Edith Rodríguez-Ortiz, Roberto Pereida-Jaramillo, Elizabeth Martínez-Torres, Ataúlfo Curr Neuropharmacol Current Neuropharmacology BACKGROUND: Danio rerio is a powerful experimental model for studies in genetics and development. Recently, CRISPR technology has been applied in this species to mimic various human diseases, including those affecting the nervous system. Zebrafish offer multiple experimental advantages: external embryogenesis, rapid development, transparent embryos, short life cycle, and basic neurobiological processes shared with humans. This animal model, together with the CRISPR system and, emerging imaging technologies, and novel behavioral approaches, lay the basis for a prominent future in neuropathology and will undoubtedly accelerate our understanding of brain function and its disorders. OBJECTIVE: Gather relevant findings from studies that have used CRISPR technologies in zebrafish to explore basic neuronal function and model human diseases. METHODS: We systematically reviewed the most recent literature about CRISPR technology applications for understanding brain function and neurological disorders in D. rerio. We highlighted the key role of CRISPR in driving forward our understanding of particular topics in neuroscience. RESULTS: We show specific advances in neurobiology when the CRISPR system has been applied in zebrafish and describe how CRISPR is accelerating our understanding of brain organization. CONCLUSION: Today, CRISPR is the preferred method to modify genomes of practically any living organism. Despite the rapid development of CRISPR technologies to generate disease models in zebrafish, more efforts are needed to efficiently combine different disciplines to find the etiology and treatments for many brain diseases. Bentham Science Publishers 2020-02 2020-02 /pmc/articles/PMC7324878/ /pubmed/31573887 http://dx.doi.org/10.2174/1570159X17666191001145550 Text en © 2020 Bentham Science Publishers https://creativecommons.org/licenses/by-nc/4.0/legalcode This is an open access article licensed under the terms of the Creative Commons Attribution-Non-Commercial 4.0 International Public License (CC BY-NC 4.0) (https://creativecommons.org/licenses/by-nc/4.0/legalcode), which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited. |
spellingShingle | Current Neuropharmacology Espino-Saldaña, Angeles Edith Rodríguez-Ortiz, Roberto Pereida-Jaramillo, Elizabeth Martínez-Torres, Ataúlfo Modeling Neuronal Diseases in Zebrafish in the Era of CRISPR |
title | Modeling Neuronal Diseases in Zebrafish in the Era of CRISPR |
title_full | Modeling Neuronal Diseases in Zebrafish in the Era of CRISPR |
title_fullStr | Modeling Neuronal Diseases in Zebrafish in the Era of CRISPR |
title_full_unstemmed | Modeling Neuronal Diseases in Zebrafish in the Era of CRISPR |
title_short | Modeling Neuronal Diseases in Zebrafish in the Era of CRISPR |
title_sort | modeling neuronal diseases in zebrafish in the era of crispr |
topic | Current Neuropharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7324878/ https://www.ncbi.nlm.nih.gov/pubmed/31573887 http://dx.doi.org/10.2174/1570159X17666191001145550 |
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