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Gene editing in monogenic autism spectrum disorder: animal models and gene therapies
Autism spectrum disorder (ASD) is a lifelong neurodevelopmental disease, and its diagnosis is dependent on behavioral manifestation, such as impaired reciprocal social interactions, stereotyped repetitive behaviors, as well as restricted interests. However, ASD etiology has eluded researchers to dat...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9794862/ https://www.ncbi.nlm.nih.gov/pubmed/36590912 http://dx.doi.org/10.3389/fnmol.2022.1043018 |
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author | Wang, Na Lv, Longbao Huang, Xiaoyi Shi, Mingqin Dai, Youwu Wei, Yuanyuan Xu, Bonan Fu, Chenyang Huang, Haoyu Shi, Hongling Liu, Yun Hu, Xintian Qin, Dongdong |
author_facet | Wang, Na Lv, Longbao Huang, Xiaoyi Shi, Mingqin Dai, Youwu Wei, Yuanyuan Xu, Bonan Fu, Chenyang Huang, Haoyu Shi, Hongling Liu, Yun Hu, Xintian Qin, Dongdong |
author_sort | Wang, Na |
collection | PubMed |
description | Autism spectrum disorder (ASD) is a lifelong neurodevelopmental disease, and its diagnosis is dependent on behavioral manifestation, such as impaired reciprocal social interactions, stereotyped repetitive behaviors, as well as restricted interests. However, ASD etiology has eluded researchers to date. In the past decades, based on strong genetic evidence including mutations in a single gene, gene editing technology has become an essential tool for exploring the pathogenetic mechanisms of ASD via constructing genetically modified animal models which validates the casual relationship between genetic risk factors and the development of ASD, thus contributing to developing ideal candidates for gene therapies. The present review discusses the progress in gene editing techniques and genetic research, animal models established by gene editing, as well as gene therapies in ASD. Future research should focus on improving the validity of animal models, and reliable DNA diagnostics and accurate prediction of the functional effects of the mutation will likely be equally crucial for the safe application of gene therapies. |
format | Online Article Text |
id | pubmed-9794862 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97948622022-12-29 Gene editing in monogenic autism spectrum disorder: animal models and gene therapies Wang, Na Lv, Longbao Huang, Xiaoyi Shi, Mingqin Dai, Youwu Wei, Yuanyuan Xu, Bonan Fu, Chenyang Huang, Haoyu Shi, Hongling Liu, Yun Hu, Xintian Qin, Dongdong Front Mol Neurosci Molecular Neuroscience Autism spectrum disorder (ASD) is a lifelong neurodevelopmental disease, and its diagnosis is dependent on behavioral manifestation, such as impaired reciprocal social interactions, stereotyped repetitive behaviors, as well as restricted interests. However, ASD etiology has eluded researchers to date. In the past decades, based on strong genetic evidence including mutations in a single gene, gene editing technology has become an essential tool for exploring the pathogenetic mechanisms of ASD via constructing genetically modified animal models which validates the casual relationship between genetic risk factors and the development of ASD, thus contributing to developing ideal candidates for gene therapies. The present review discusses the progress in gene editing techniques and genetic research, animal models established by gene editing, as well as gene therapies in ASD. Future research should focus on improving the validity of animal models, and reliable DNA diagnostics and accurate prediction of the functional effects of the mutation will likely be equally crucial for the safe application of gene therapies. Frontiers Media S.A. 2022-12-14 /pmc/articles/PMC9794862/ /pubmed/36590912 http://dx.doi.org/10.3389/fnmol.2022.1043018 Text en Copyright © 2022 Wang, Lv, Huang, Shi, Dai, Wei, Xu, Fu, Huang, Shi, Liu, Hu and Qin. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Molecular Neuroscience Wang, Na Lv, Longbao Huang, Xiaoyi Shi, Mingqin Dai, Youwu Wei, Yuanyuan Xu, Bonan Fu, Chenyang Huang, Haoyu Shi, Hongling Liu, Yun Hu, Xintian Qin, Dongdong Gene editing in monogenic autism spectrum disorder: animal models and gene therapies |
title | Gene editing in monogenic autism spectrum disorder: animal models and gene therapies |
title_full | Gene editing in monogenic autism spectrum disorder: animal models and gene therapies |
title_fullStr | Gene editing in monogenic autism spectrum disorder: animal models and gene therapies |
title_full_unstemmed | Gene editing in monogenic autism spectrum disorder: animal models and gene therapies |
title_short | Gene editing in monogenic autism spectrum disorder: animal models and gene therapies |
title_sort | gene editing in monogenic autism spectrum disorder: animal models and gene therapies |
topic | Molecular Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9794862/ https://www.ncbi.nlm.nih.gov/pubmed/36590912 http://dx.doi.org/10.3389/fnmol.2022.1043018 |
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