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Increased Variability of Genomic Transcription in Schizophrenia

Schizophrenia (SZ) is a severe chronic mental disorder with a high heritability. Current microarray analyses typically focus on identifying differentially expressed genes or enriched pathways relevant to phenotypes. Whether there is a variability change of the genomic transcription in diseases has r...

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Autores principales: Zhang, Fuquan, Yao Shugart, Yin, Yue, Weihua, Cheng, Zaohuo, Wang, Guoqiang, Zhou, Zhenhe, Jin, Chunhui, Yuan, Jianmin, Liu, Sha, Xu, Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4675071/
https://www.ncbi.nlm.nih.gov/pubmed/26657146
http://dx.doi.org/10.1038/srep17995
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author Zhang, Fuquan
Yao Shugart, Yin
Yue, Weihua
Cheng, Zaohuo
Wang, Guoqiang
Zhou, Zhenhe
Jin, Chunhui
Yuan, Jianmin
Liu, Sha
Xu, Yong
author_facet Zhang, Fuquan
Yao Shugart, Yin
Yue, Weihua
Cheng, Zaohuo
Wang, Guoqiang
Zhou, Zhenhe
Jin, Chunhui
Yuan, Jianmin
Liu, Sha
Xu, Yong
author_sort Zhang, Fuquan
collection PubMed
description Schizophrenia (SZ) is a severe chronic mental disorder with a high heritability. Current microarray analyses typically focus on identifying differentially expressed genes or enriched pathways relevant to phenotypes. Whether there is a variability change of the genomic transcription in diseases has rarely been explored. In this study, we compared coefficient of variation (CV, the ratio of the standard deviation to the mean) of genome transcription of early-onset SZ (EOS) patients with controls in a blood mRNA microarray dataset and a blood microRNA (miRNA) microarray dataset. Furthermore, we compared CV of the expression levels of 17 genes in blood of the 30 patients before and after the 12-week treatment using real-time quantitative PCR (RT-qPCR) analysis. Our results indicated a significant increase of CV of genome transcription in patients compared with controls in both the mRNA and the miRNA datasets. The 30 after-treatment patients showed a significant decrease of CV of gene expression compared with the before-treatment patients. Our study may implicate the blood gene expression variability in SZ, providing further evidence supporting the abnormality of peripheral blood transcriptome in SZ. Given that peripheral blood can be easily collected from patients and followed longitudinally, our results may indicate a new way to facilitate the identification of the signatures of clinical subtypes, their prognosis and treatment response.
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spelling pubmed-46750712015-12-16 Increased Variability of Genomic Transcription in Schizophrenia Zhang, Fuquan Yao Shugart, Yin Yue, Weihua Cheng, Zaohuo Wang, Guoqiang Zhou, Zhenhe Jin, Chunhui Yuan, Jianmin Liu, Sha Xu, Yong Sci Rep Article Schizophrenia (SZ) is a severe chronic mental disorder with a high heritability. Current microarray analyses typically focus on identifying differentially expressed genes or enriched pathways relevant to phenotypes. Whether there is a variability change of the genomic transcription in diseases has rarely been explored. In this study, we compared coefficient of variation (CV, the ratio of the standard deviation to the mean) of genome transcription of early-onset SZ (EOS) patients with controls in a blood mRNA microarray dataset and a blood microRNA (miRNA) microarray dataset. Furthermore, we compared CV of the expression levels of 17 genes in blood of the 30 patients before and after the 12-week treatment using real-time quantitative PCR (RT-qPCR) analysis. Our results indicated a significant increase of CV of genome transcription in patients compared with controls in both the mRNA and the miRNA datasets. The 30 after-treatment patients showed a significant decrease of CV of gene expression compared with the before-treatment patients. Our study may implicate the blood gene expression variability in SZ, providing further evidence supporting the abnormality of peripheral blood transcriptome in SZ. Given that peripheral blood can be easily collected from patients and followed longitudinally, our results may indicate a new way to facilitate the identification of the signatures of clinical subtypes, their prognosis and treatment response. Nature Publishing Group 2015-12-10 /pmc/articles/PMC4675071/ /pubmed/26657146 http://dx.doi.org/10.1038/srep17995 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Zhang, Fuquan
Yao Shugart, Yin
Yue, Weihua
Cheng, Zaohuo
Wang, Guoqiang
Zhou, Zhenhe
Jin, Chunhui
Yuan, Jianmin
Liu, Sha
Xu, Yong
Increased Variability of Genomic Transcription in Schizophrenia
title Increased Variability of Genomic Transcription in Schizophrenia
title_full Increased Variability of Genomic Transcription in Schizophrenia
title_fullStr Increased Variability of Genomic Transcription in Schizophrenia
title_full_unstemmed Increased Variability of Genomic Transcription in Schizophrenia
title_short Increased Variability of Genomic Transcription in Schizophrenia
title_sort increased variability of genomic transcription in schizophrenia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4675071/
https://www.ncbi.nlm.nih.gov/pubmed/26657146
http://dx.doi.org/10.1038/srep17995
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