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DNA hypomethylation of Synapsin II CpG islands associates with increased gene expression in bipolar disorder and major depression
BACKGROUND: The Synapsins (SYN1, SYN2, and SYN3) are important players in the adult brain, given their involvement in synaptic transmission and plasticity, as well as in the developing brain through roles in axon outgrowth and synaptogenesis. We and others previously reported gene expression dysregu...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4982122/ https://www.ncbi.nlm.nih.gov/pubmed/27515700 http://dx.doi.org/10.1186/s12888-016-0989-0 |
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author | Cruceanu, Cristiana Kutsarova, Elena Chen, Elizabeth S. Checknita, David R. Nagy, Corina Lopez, Juan Pablo Alda, Martin Rouleau, Guy A. Turecki, Gustavo |
author_facet | Cruceanu, Cristiana Kutsarova, Elena Chen, Elizabeth S. Checknita, David R. Nagy, Corina Lopez, Juan Pablo Alda, Martin Rouleau, Guy A. Turecki, Gustavo |
author_sort | Cruceanu, Cristiana |
collection | PubMed |
description | BACKGROUND: The Synapsins (SYN1, SYN2, and SYN3) are important players in the adult brain, given their involvement in synaptic transmission and plasticity, as well as in the developing brain through roles in axon outgrowth and synaptogenesis. We and others previously reported gene expression dysregulation, both as increases and decreases, of Synapsins in mood disorders, but little is known about the regulatory mechanisms leading to these differences. Thus, we proposed to study DNA methylation at theses genes’ promoter regions, under the assumption that altered epigenetic marks at key regulatory sites would be the cause of gene expression changes and thus part of the mood disorder etiology. METHODS: We performed CpG methylation mapping focusing on the three genes’ predicted CpG islands using the Sequenom EpiTYPER platform. DNA extracted from post-mortem brain tissue (BA10) from individuals who had lived with bipolar disorder (BD), major depressive disorder (MDD), as well as psychiatrically healthy individuals was used. Differences in methylation across all CpGs within a CpG island and between the three diagnostic groups were assessed by 2-way mixed model analyses of variance. RESULTS: We found no significant results for SYN1 or SYN3, but there was a significant group difference in SYN2 methylation, as well as an overall pattern of hypomethylation across the CpG island. Furthermore, we found a significant inverse correlation of DNA methylation with SYN2a mRNA expression. CONCLUSIONS: These findings contribute to previous work showing dysregulation of Synapsins, particularly SYN2, in mood disorders and improve our understanding of the regulatory mechanisms that precipitate these changes likely leading to the BD or MDD phenotype. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12888-016-0989-0) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4982122 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-49821222016-08-13 DNA hypomethylation of Synapsin II CpG islands associates with increased gene expression in bipolar disorder and major depression Cruceanu, Cristiana Kutsarova, Elena Chen, Elizabeth S. Checknita, David R. Nagy, Corina Lopez, Juan Pablo Alda, Martin Rouleau, Guy A. Turecki, Gustavo BMC Psychiatry Research Article BACKGROUND: The Synapsins (SYN1, SYN2, and SYN3) are important players in the adult brain, given their involvement in synaptic transmission and plasticity, as well as in the developing brain through roles in axon outgrowth and synaptogenesis. We and others previously reported gene expression dysregulation, both as increases and decreases, of Synapsins in mood disorders, but little is known about the regulatory mechanisms leading to these differences. Thus, we proposed to study DNA methylation at theses genes’ promoter regions, under the assumption that altered epigenetic marks at key regulatory sites would be the cause of gene expression changes and thus part of the mood disorder etiology. METHODS: We performed CpG methylation mapping focusing on the three genes’ predicted CpG islands using the Sequenom EpiTYPER platform. DNA extracted from post-mortem brain tissue (BA10) from individuals who had lived with bipolar disorder (BD), major depressive disorder (MDD), as well as psychiatrically healthy individuals was used. Differences in methylation across all CpGs within a CpG island and between the three diagnostic groups were assessed by 2-way mixed model analyses of variance. RESULTS: We found no significant results for SYN1 or SYN3, but there was a significant group difference in SYN2 methylation, as well as an overall pattern of hypomethylation across the CpG island. Furthermore, we found a significant inverse correlation of DNA methylation with SYN2a mRNA expression. CONCLUSIONS: These findings contribute to previous work showing dysregulation of Synapsins, particularly SYN2, in mood disorders and improve our understanding of the regulatory mechanisms that precipitate these changes likely leading to the BD or MDD phenotype. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12888-016-0989-0) contains supplementary material, which is available to authorized users. BioMed Central 2016-08-11 /pmc/articles/PMC4982122/ /pubmed/27515700 http://dx.doi.org/10.1186/s12888-016-0989-0 Text en © The Author(s). 2016 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 Cruceanu, Cristiana Kutsarova, Elena Chen, Elizabeth S. Checknita, David R. Nagy, Corina Lopez, Juan Pablo Alda, Martin Rouleau, Guy A. Turecki, Gustavo DNA hypomethylation of Synapsin II CpG islands associates with increased gene expression in bipolar disorder and major depression |
title | DNA hypomethylation of Synapsin II CpG islands associates with increased gene expression in bipolar disorder and major depression |
title_full | DNA hypomethylation of Synapsin II CpG islands associates with increased gene expression in bipolar disorder and major depression |
title_fullStr | DNA hypomethylation of Synapsin II CpG islands associates with increased gene expression in bipolar disorder and major depression |
title_full_unstemmed | DNA hypomethylation of Synapsin II CpG islands associates with increased gene expression in bipolar disorder and major depression |
title_short | DNA hypomethylation of Synapsin II CpG islands associates with increased gene expression in bipolar disorder and major depression |
title_sort | dna hypomethylation of synapsin ii cpg islands associates with increased gene expression in bipolar disorder and major depression |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4982122/ https://www.ncbi.nlm.nih.gov/pubmed/27515700 http://dx.doi.org/10.1186/s12888-016-0989-0 |
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