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Developmental profiling of ASD-related shank3 transcripts and their differential regulation by valproic acid in zebrafish
SHANK3 is a scaffolding protein that binds to various synaptic proteins at the postsynaptic density (PSD) of excitatory glutamatergic synapses. SHANK3 is not only strongly implicated in autism spectrum disorders (ASD) but also plays a critical role in human Phelan-McDermid syndrome (22q13.3 deletion...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5099374/ https://www.ncbi.nlm.nih.gov/pubmed/27562614 http://dx.doi.org/10.1007/s00427-016-0561-4 |
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author | Liu, Chun-xue Peng, Xiao-lan Hu, Chun-chun Li, Chun-yang Li, Qiang Xu, Xiu |
author_facet | Liu, Chun-xue Peng, Xiao-lan Hu, Chun-chun Li, Chun-yang Li, Qiang Xu, Xiu |
author_sort | Liu, Chun-xue |
collection | PubMed |
description | SHANK3 is a scaffolding protein that binds to various synaptic proteins at the postsynaptic density (PSD) of excitatory glutamatergic synapses. SHANK3 is not only strongly implicated in autism spectrum disorders (ASD) but also plays a critical role in human Phelan-McDermid syndrome (22q13.3 deletion syndrome). Accumulated experimental evidence demonstrates that the zebrafish model system is useful for studying the functions of ASD-related gene during early development. However, many basic features of shank3 transcript expression in zebrafish remain poorly understood. Here, we investigated temporal, spatial, and isoform-specific expression patterns of shank3 during zebrafish development on the basis of previous researches and the differential effects of each shank3 transcript expression after exposure to valproic acid (VPA), an ASD-associated drug. At first, we observed that both shank3a and shank3b were barely expressed at very early ages (before 24 h post-fertilization (hpf)), whereas their expression levels were increased and mainly enriched in the nervous system after 24 hpf. Secondly, all of the six shank3 transcripts gradually increased during the first 7 hpf and then decreased. Subsequently, they exhibited a second increasing peak between 1 month post-fertilization (mpf) and adulthood. Thirdly, VPA treatment affected the isoform-specific expression of zebrafish shank3. In particular, the mRNA expression levels of those isoforms that contain a SAM domain were significantly increased, whereas the mRNA expression level of those which contained an ANK domain but without a SAM domain was decreased. To conclude, our findings support the molecular diversity of shank3 in zebrafish and provide a molecular framework to understand the isoform-specific function of shank3 in zebrafish. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00427-016-0561-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5099374 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-50993742016-11-21 Developmental profiling of ASD-related shank3 transcripts and their differential regulation by valproic acid in zebrafish Liu, Chun-xue Peng, Xiao-lan Hu, Chun-chun Li, Chun-yang Li, Qiang Xu, Xiu Dev Genes Evol Original Article SHANK3 is a scaffolding protein that binds to various synaptic proteins at the postsynaptic density (PSD) of excitatory glutamatergic synapses. SHANK3 is not only strongly implicated in autism spectrum disorders (ASD) but also plays a critical role in human Phelan-McDermid syndrome (22q13.3 deletion syndrome). Accumulated experimental evidence demonstrates that the zebrafish model system is useful for studying the functions of ASD-related gene during early development. However, many basic features of shank3 transcript expression in zebrafish remain poorly understood. Here, we investigated temporal, spatial, and isoform-specific expression patterns of shank3 during zebrafish development on the basis of previous researches and the differential effects of each shank3 transcript expression after exposure to valproic acid (VPA), an ASD-associated drug. At first, we observed that both shank3a and shank3b were barely expressed at very early ages (before 24 h post-fertilization (hpf)), whereas their expression levels were increased and mainly enriched in the nervous system after 24 hpf. Secondly, all of the six shank3 transcripts gradually increased during the first 7 hpf and then decreased. Subsequently, they exhibited a second increasing peak between 1 month post-fertilization (mpf) and adulthood. Thirdly, VPA treatment affected the isoform-specific expression of zebrafish shank3. In particular, the mRNA expression levels of those isoforms that contain a SAM domain were significantly increased, whereas the mRNA expression level of those which contained an ANK domain but without a SAM domain was decreased. To conclude, our findings support the molecular diversity of shank3 in zebrafish and provide a molecular framework to understand the isoform-specific function of shank3 in zebrafish. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00427-016-0561-4) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2016-08-26 2016 /pmc/articles/PMC5099374/ /pubmed/27562614 http://dx.doi.org/10.1007/s00427-016-0561-4 Text en © The Author(s) 2016 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Article Liu, Chun-xue Peng, Xiao-lan Hu, Chun-chun Li, Chun-yang Li, Qiang Xu, Xiu Developmental profiling of ASD-related shank3 transcripts and their differential regulation by valproic acid in zebrafish |
title | Developmental profiling of ASD-related shank3 transcripts and their differential regulation by valproic acid in zebrafish |
title_full | Developmental profiling of ASD-related shank3 transcripts and their differential regulation by valproic acid in zebrafish |
title_fullStr | Developmental profiling of ASD-related shank3 transcripts and their differential regulation by valproic acid in zebrafish |
title_full_unstemmed | Developmental profiling of ASD-related shank3 transcripts and their differential regulation by valproic acid in zebrafish |
title_short | Developmental profiling of ASD-related shank3 transcripts and their differential regulation by valproic acid in zebrafish |
title_sort | developmental profiling of asd-related shank3 transcripts and their differential regulation by valproic acid in zebrafish |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5099374/ https://www.ncbi.nlm.nih.gov/pubmed/27562614 http://dx.doi.org/10.1007/s00427-016-0561-4 |
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