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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...

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Autores principales: Liu, Chun-xue, Peng, Xiao-lan, Hu, Chun-chun, Li, Chun-yang, Li, Qiang, Xu, Xiu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2016
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.
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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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