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Genome-wide DNA methylome reveals the dysfunction of intronic microRNAs in major psychosis
BACKGROUND: DNA methylation is thought to be extensively involved in the pathogenesis of many diseases, including major psychosis. However, most studies focus on DNA methylation alteration at promoters of protein-coding genes, despite the poor correlation between DNA methylation and gene expression....
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4604612/ https://www.ncbi.nlm.nih.gov/pubmed/26462620 http://dx.doi.org/10.1186/s12920-015-0139-4 |
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author | Zhao, Hongying Xu, Jinyuan Pang, Lin Zhang, Yunpeng Fan, Huihui Liu, Ling Liu, Tingting Yu, Fulong Zhang, Guanxiong Lan, Yujia Bai, Jing Li, Xia Xiao, Yun |
author_facet | Zhao, Hongying Xu, Jinyuan Pang, Lin Zhang, Yunpeng Fan, Huihui Liu, Ling Liu, Tingting Yu, Fulong Zhang, Guanxiong Lan, Yujia Bai, Jing Li, Xia Xiao, Yun |
author_sort | Zhao, Hongying |
collection | PubMed |
description | BACKGROUND: DNA methylation is thought to be extensively involved in the pathogenesis of many diseases, including major psychosis. However, most studies focus on DNA methylation alteration at promoters of protein-coding genes, despite the poor correlation between DNA methylation and gene expression. METHODS: We analyzed differentially methylated regions and differentially expressed genes in patients with schizophrenia and bipolar disorder and normal subjects. Gene expression and DNA methylation were analyzed with RNA-seq and MeDIP-seq of post-mortem brain tissue (brain region BA9) cohort in five schizophrenia, seven bipolar disorder cases and six controls, respectively. RESULTS: Here, we performed a large-scale integrative analysis using MeDIP-seq, coupled with RNA-seq, on brain samples from major psychotic and normal subjects and observed obvious discrepancy between DNA methylation and gene expression. We found that differentially methylated regions (DMRs) were distributed across different types of genomic elements, especially introns. These intronic DMRs were significantly enriched for diverse regulatory elements, such as enhancers and binding sites of certain transcriptional factors (e.g., Pol3). Notably, we found that parts of intronic DMRs overlapped with some intragenic miRNAs, such as hsa-mir-7-3. These intronic DMR-related miRNAs were found to target many differentially expressed genes. Moreover, functional analysis demonstrated that differential target genes of intronic DMR-related miRNAs were sufficient to capture many important biological processes in major psychosis, such as neurogenesis, suggesting that miRNAs may function as important linkers mediating the relationships between DNA methylation alteration and gene expression changes. CONCLUSIONS: Collectively, our study indicated that DNA methylation alteration could induce expression changes indirectly by affecting miRNAs and the exploration of DMR-related miRNAs and their targets enhanced understanding of the molecular mechanisms underlying major psychosis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12920-015-0139-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4604612 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-46046122015-10-15 Genome-wide DNA methylome reveals the dysfunction of intronic microRNAs in major psychosis Zhao, Hongying Xu, Jinyuan Pang, Lin Zhang, Yunpeng Fan, Huihui Liu, Ling Liu, Tingting Yu, Fulong Zhang, Guanxiong Lan, Yujia Bai, Jing Li, Xia Xiao, Yun BMC Med Genomics Research Article BACKGROUND: DNA methylation is thought to be extensively involved in the pathogenesis of many diseases, including major psychosis. However, most studies focus on DNA methylation alteration at promoters of protein-coding genes, despite the poor correlation between DNA methylation and gene expression. METHODS: We analyzed differentially methylated regions and differentially expressed genes in patients with schizophrenia and bipolar disorder and normal subjects. Gene expression and DNA methylation were analyzed with RNA-seq and MeDIP-seq of post-mortem brain tissue (brain region BA9) cohort in five schizophrenia, seven bipolar disorder cases and six controls, respectively. RESULTS: Here, we performed a large-scale integrative analysis using MeDIP-seq, coupled with RNA-seq, on brain samples from major psychotic and normal subjects and observed obvious discrepancy between DNA methylation and gene expression. We found that differentially methylated regions (DMRs) were distributed across different types of genomic elements, especially introns. These intronic DMRs were significantly enriched for diverse regulatory elements, such as enhancers and binding sites of certain transcriptional factors (e.g., Pol3). Notably, we found that parts of intronic DMRs overlapped with some intragenic miRNAs, such as hsa-mir-7-3. These intronic DMR-related miRNAs were found to target many differentially expressed genes. Moreover, functional analysis demonstrated that differential target genes of intronic DMR-related miRNAs were sufficient to capture many important biological processes in major psychosis, such as neurogenesis, suggesting that miRNAs may function as important linkers mediating the relationships between DNA methylation alteration and gene expression changes. CONCLUSIONS: Collectively, our study indicated that DNA methylation alteration could induce expression changes indirectly by affecting miRNAs and the exploration of DMR-related miRNAs and their targets enhanced understanding of the molecular mechanisms underlying major psychosis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12920-015-0139-4) contains supplementary material, which is available to authorized users. BioMed Central 2015-10-14 /pmc/articles/PMC4604612/ /pubmed/26462620 http://dx.doi.org/10.1186/s12920-015-0139-4 Text en © Zhao et al. 2015 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 Zhao, Hongying Xu, Jinyuan Pang, Lin Zhang, Yunpeng Fan, Huihui Liu, Ling Liu, Tingting Yu, Fulong Zhang, Guanxiong Lan, Yujia Bai, Jing Li, Xia Xiao, Yun Genome-wide DNA methylome reveals the dysfunction of intronic microRNAs in major psychosis |
title | Genome-wide DNA methylome reveals the dysfunction of intronic microRNAs in major psychosis |
title_full | Genome-wide DNA methylome reveals the dysfunction of intronic microRNAs in major psychosis |
title_fullStr | Genome-wide DNA methylome reveals the dysfunction of intronic microRNAs in major psychosis |
title_full_unstemmed | Genome-wide DNA methylome reveals the dysfunction of intronic microRNAs in major psychosis |
title_short | Genome-wide DNA methylome reveals the dysfunction of intronic microRNAs in major psychosis |
title_sort | genome-wide dna methylome reveals the dysfunction of intronic micrornas in major psychosis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4604612/ https://www.ncbi.nlm.nih.gov/pubmed/26462620 http://dx.doi.org/10.1186/s12920-015-0139-4 |
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