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Identification of schizophrenia symptom-related gene modules by postmortem brain transcriptome analysis
Schizophrenia is a multifactorial disorder, the genetic architecture of which remains unclear. Although many studies have examined the etiology of schizophrenia, the gene sets that contribute to its symptoms have not been fully investigated. In this study, we aimed to identify each gene set associat...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10160042/ https://www.ncbi.nlm.nih.gov/pubmed/37142572 http://dx.doi.org/10.1038/s41398-023-02449-8 |
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author | Miyahara, Kazusa Hino, Mizuki Shishido, Risa Nagaoka, Atsuko Izumi, Ryuta Hayashi, Hideki Kakita, Akiyoshi Yabe, Hirooki Tomita, Hiroaki Kunii, Yasuto |
author_facet | Miyahara, Kazusa Hino, Mizuki Shishido, Risa Nagaoka, Atsuko Izumi, Ryuta Hayashi, Hideki Kakita, Akiyoshi Yabe, Hirooki Tomita, Hiroaki Kunii, Yasuto |
author_sort | Miyahara, Kazusa |
collection | PubMed |
description | Schizophrenia is a multifactorial disorder, the genetic architecture of which remains unclear. Although many studies have examined the etiology of schizophrenia, the gene sets that contribute to its symptoms have not been fully investigated. In this study, we aimed to identify each gene set associated with corresponding symptoms of schizophrenia using the postmortem brains of 26 patients with schizophrenia and 51 controls. We classified genes expressed in the prefrontal cortex (analyzed by RNA-seq) into several modules by weighted gene co-expression network analysis (WGCNA) and examined the correlation between module expression and clinical characteristics. In addition, we calculated the polygenic risk score (PRS) for schizophrenia from Japanese genome-wide association studies, and investigated the association between the identified gene modules and PRS to evaluate whether genetic background affected gene expression. Finally, we conducted pathway analysis and upstream analysis using Ingenuity Pathway Analysis to clarify the functions and upstream regulators of symptom-related gene modules. As a result, three gene modules generated by WGCNA were significantly correlated with clinical characteristics, and one of these showed a significant association with PRS. Genes belonging to the transcriptional module associated with PRS significantly overlapped with signaling pathways of multiple sclerosis, neuroinflammation, and opioid use, suggesting that these pathways may also be profoundly implicated in schizophrenia. Upstream analysis indicated that genes in the detected module were profoundly regulated by lipopolysaccharides and CREB. This study identified schizophrenia symptom-related gene sets and their upstream regulators, revealing aspects of the pathophysiology of schizophrenia and identifying potential therapeutic targets. |
format | Online Article Text |
id | pubmed-10160042 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-101600422023-05-06 Identification of schizophrenia symptom-related gene modules by postmortem brain transcriptome analysis Miyahara, Kazusa Hino, Mizuki Shishido, Risa Nagaoka, Atsuko Izumi, Ryuta Hayashi, Hideki Kakita, Akiyoshi Yabe, Hirooki Tomita, Hiroaki Kunii, Yasuto Transl Psychiatry Article Schizophrenia is a multifactorial disorder, the genetic architecture of which remains unclear. Although many studies have examined the etiology of schizophrenia, the gene sets that contribute to its symptoms have not been fully investigated. In this study, we aimed to identify each gene set associated with corresponding symptoms of schizophrenia using the postmortem brains of 26 patients with schizophrenia and 51 controls. We classified genes expressed in the prefrontal cortex (analyzed by RNA-seq) into several modules by weighted gene co-expression network analysis (WGCNA) and examined the correlation between module expression and clinical characteristics. In addition, we calculated the polygenic risk score (PRS) for schizophrenia from Japanese genome-wide association studies, and investigated the association between the identified gene modules and PRS to evaluate whether genetic background affected gene expression. Finally, we conducted pathway analysis and upstream analysis using Ingenuity Pathway Analysis to clarify the functions and upstream regulators of symptom-related gene modules. As a result, three gene modules generated by WGCNA were significantly correlated with clinical characteristics, and one of these showed a significant association with PRS. Genes belonging to the transcriptional module associated with PRS significantly overlapped with signaling pathways of multiple sclerosis, neuroinflammation, and opioid use, suggesting that these pathways may also be profoundly implicated in schizophrenia. Upstream analysis indicated that genes in the detected module were profoundly regulated by lipopolysaccharides and CREB. This study identified schizophrenia symptom-related gene sets and their upstream regulators, revealing aspects of the pathophysiology of schizophrenia and identifying potential therapeutic targets. Nature Publishing Group UK 2023-05-04 /pmc/articles/PMC10160042/ /pubmed/37142572 http://dx.doi.org/10.1038/s41398-023-02449-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Miyahara, Kazusa Hino, Mizuki Shishido, Risa Nagaoka, Atsuko Izumi, Ryuta Hayashi, Hideki Kakita, Akiyoshi Yabe, Hirooki Tomita, Hiroaki Kunii, Yasuto Identification of schizophrenia symptom-related gene modules by postmortem brain transcriptome analysis |
title | Identification of schizophrenia symptom-related gene modules by postmortem brain transcriptome analysis |
title_full | Identification of schizophrenia symptom-related gene modules by postmortem brain transcriptome analysis |
title_fullStr | Identification of schizophrenia symptom-related gene modules by postmortem brain transcriptome analysis |
title_full_unstemmed | Identification of schizophrenia symptom-related gene modules by postmortem brain transcriptome analysis |
title_short | Identification of schizophrenia symptom-related gene modules by postmortem brain transcriptome analysis |
title_sort | identification of schizophrenia symptom-related gene modules by postmortem brain transcriptome analysis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10160042/ https://www.ncbi.nlm.nih.gov/pubmed/37142572 http://dx.doi.org/10.1038/s41398-023-02449-8 |
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