Cargando…

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....

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
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
_version_ 1782395073013481472
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
work_keys_str_mv AT zhaohongying genomewidednamethylomerevealsthedysfunctionofintronicmicrornasinmajorpsychosis
AT xujinyuan genomewidednamethylomerevealsthedysfunctionofintronicmicrornasinmajorpsychosis
AT panglin genomewidednamethylomerevealsthedysfunctionofintronicmicrornasinmajorpsychosis
AT zhangyunpeng genomewidednamethylomerevealsthedysfunctionofintronicmicrornasinmajorpsychosis
AT fanhuihui genomewidednamethylomerevealsthedysfunctionofintronicmicrornasinmajorpsychosis
AT liuling genomewidednamethylomerevealsthedysfunctionofintronicmicrornasinmajorpsychosis
AT liutingting genomewidednamethylomerevealsthedysfunctionofintronicmicrornasinmajorpsychosis
AT yufulong genomewidednamethylomerevealsthedysfunctionofintronicmicrornasinmajorpsychosis
AT zhangguanxiong genomewidednamethylomerevealsthedysfunctionofintronicmicrornasinmajorpsychosis
AT lanyujia genomewidednamethylomerevealsthedysfunctionofintronicmicrornasinmajorpsychosis
AT baijing genomewidednamethylomerevealsthedysfunctionofintronicmicrornasinmajorpsychosis
AT lixia genomewidednamethylomerevealsthedysfunctionofintronicmicrornasinmajorpsychosis
AT xiaoyun genomewidednamethylomerevealsthedysfunctionofintronicmicrornasinmajorpsychosis