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Expression of alternatively spliced variants of the Dclk1 gene is regulated by psychotropic drugs

BACKGROUND: The long-term effects of psychotropic drugs are associated with the reversal of disease-related alterations through the reorganization and normalization of neuronal connections. Molecular factors that trigger drug-induced brain plasticity remain only partly understood. Doublecortin-like...

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Autores principales: Zygmunt, Magdalena, Hoinkis, Dżesika, Hajto, Jacek, Piechota, Marcin, Skupień-Rabian, Bożena, Jankowska, Urszula, Kędracka-Krok, Sylwia, Rodriguez Parkitna, Jan, Korostyński, Michał
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6134793/
https://www.ncbi.nlm.nih.gov/pubmed/30208879
http://dx.doi.org/10.1186/s12868-018-0458-4
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author Zygmunt, Magdalena
Hoinkis, Dżesika
Hajto, Jacek
Piechota, Marcin
Skupień-Rabian, Bożena
Jankowska, Urszula
Kędracka-Krok, Sylwia
Rodriguez Parkitna, Jan
Korostyński, Michał
author_facet Zygmunt, Magdalena
Hoinkis, Dżesika
Hajto, Jacek
Piechota, Marcin
Skupień-Rabian, Bożena
Jankowska, Urszula
Kędracka-Krok, Sylwia
Rodriguez Parkitna, Jan
Korostyński, Michał
author_sort Zygmunt, Magdalena
collection PubMed
description BACKGROUND: The long-term effects of psychotropic drugs are associated with the reversal of disease-related alterations through the reorganization and normalization of neuronal connections. Molecular factors that trigger drug-induced brain plasticity remain only partly understood. Doublecortin-like kinase 1 (Dclk1) possesses microtubule-polymerizing activity during synaptic plasticity and neurogenesis. However, the Dclk1 gene shows a complex profile of transcriptional regulation, with two alternative promoters and exon splicing patterns that suggest the expression of multiple isoforms with different kinase activities. RESULTS: Here, we applied next-generation sequencing to analyze changes in the expression of Dclk1 gene isoforms in the brain in response to several psychoactive drugs with diverse pharmacological mechanisms of action. We used bioinformatics tools to define the range and levels of Dclk1 transcriptional regulation in the mouse nucleus accumbens and prefrontal cortex. We also sought to investigate the presence of DCLK1-derived peptides using mass spectrometry. We detected 15 transcripts expressed from the Dclk1 locus (FPKM > 1), including 2 drug-regulated variants (fold change > 2). Drugs that act on serotonin receptors (5-HT2A/C) regulate a subset of Dclk1 isoforms in a brain-region-specific manner. The strongest influence was observed for the mianserin-induced expression of an isoform with intron retention. The drug-activated expression of novel alternative Dclk1 isoforms was validated using qPCR. The drug-regulated isoform contains genetic variants of DCLK1 that have been previously associated with schizophrenia and hyperactivity disorder in humans. We identified a short peptide that might originate from the novel DCLK1 protein product. Moreover, protein domains encoded by the regulated variant indicate their potential involvement in the negative regulation of the canonical DCLK1 protein. CONCLUSIONS: In summary, we identified novel isoforms of the neuroplasticity-related gene Dclk1 that are expressed in the brain in response to psychotropic drug treatments. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12868-018-0458-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-61347932018-09-15 Expression of alternatively spliced variants of the Dclk1 gene is regulated by psychotropic drugs Zygmunt, Magdalena Hoinkis, Dżesika Hajto, Jacek Piechota, Marcin Skupień-Rabian, Bożena Jankowska, Urszula Kędracka-Krok, Sylwia Rodriguez Parkitna, Jan Korostyński, Michał BMC Neurosci Research Article BACKGROUND: The long-term effects of psychotropic drugs are associated with the reversal of disease-related alterations through the reorganization and normalization of neuronal connections. Molecular factors that trigger drug-induced brain plasticity remain only partly understood. Doublecortin-like kinase 1 (Dclk1) possesses microtubule-polymerizing activity during synaptic plasticity and neurogenesis. However, the Dclk1 gene shows a complex profile of transcriptional regulation, with two alternative promoters and exon splicing patterns that suggest the expression of multiple isoforms with different kinase activities. RESULTS: Here, we applied next-generation sequencing to analyze changes in the expression of Dclk1 gene isoforms in the brain in response to several psychoactive drugs with diverse pharmacological mechanisms of action. We used bioinformatics tools to define the range and levels of Dclk1 transcriptional regulation in the mouse nucleus accumbens and prefrontal cortex. We also sought to investigate the presence of DCLK1-derived peptides using mass spectrometry. We detected 15 transcripts expressed from the Dclk1 locus (FPKM > 1), including 2 drug-regulated variants (fold change > 2). Drugs that act on serotonin receptors (5-HT2A/C) regulate a subset of Dclk1 isoforms in a brain-region-specific manner. The strongest influence was observed for the mianserin-induced expression of an isoform with intron retention. The drug-activated expression of novel alternative Dclk1 isoforms was validated using qPCR. The drug-regulated isoform contains genetic variants of DCLK1 that have been previously associated with schizophrenia and hyperactivity disorder in humans. We identified a short peptide that might originate from the novel DCLK1 protein product. Moreover, protein domains encoded by the regulated variant indicate their potential involvement in the negative regulation of the canonical DCLK1 protein. CONCLUSIONS: In summary, we identified novel isoforms of the neuroplasticity-related gene Dclk1 that are expressed in the brain in response to psychotropic drug treatments. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12868-018-0458-4) contains supplementary material, which is available to authorized users. BioMed Central 2018-09-12 /pmc/articles/PMC6134793/ /pubmed/30208879 http://dx.doi.org/10.1186/s12868-018-0458-4 Text en © The Author(s) 2018 Open AccessThis 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Zygmunt, Magdalena
Hoinkis, Dżesika
Hajto, Jacek
Piechota, Marcin
Skupień-Rabian, Bożena
Jankowska, Urszula
Kędracka-Krok, Sylwia
Rodriguez Parkitna, Jan
Korostyński, Michał
Expression of alternatively spliced variants of the Dclk1 gene is regulated by psychotropic drugs
title Expression of alternatively spliced variants of the Dclk1 gene is regulated by psychotropic drugs
title_full Expression of alternatively spliced variants of the Dclk1 gene is regulated by psychotropic drugs
title_fullStr Expression of alternatively spliced variants of the Dclk1 gene is regulated by psychotropic drugs
title_full_unstemmed Expression of alternatively spliced variants of the Dclk1 gene is regulated by psychotropic drugs
title_short Expression of alternatively spliced variants of the Dclk1 gene is regulated by psychotropic drugs
title_sort expression of alternatively spliced variants of the dclk1 gene is regulated by psychotropic drugs
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6134793/
https://www.ncbi.nlm.nih.gov/pubmed/30208879
http://dx.doi.org/10.1186/s12868-018-0458-4
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