Identification of lncRNA NR_028138.1 as a biomarker and construction of a ceRNA network for bipolar disorder

Abstract The pathogenesis of bipolar disorder (BD), a chronic mood disorder, is largely unknown. Noncoding RNAs play important roles in the pathogenesis of BD. However, little is known about the correlations of long noncoding RNAs (lncRNAs) with BD. Illumina high-throughput sequencing in BD patients...

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Autores principales: Ling He, Pengtao Zou, Wanlei Sun, Yonghui Fu, Wenfeng He, Juxiang Li
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Publicado: Nature Portfolio 2021
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spelling oai:doaj.org-article:79da7f272838489a822acb273f1d0efa2021-12-02T16:34:05ZIdentification of lncRNA NR_028138.1 as a biomarker and construction of a ceRNA network for bipolar disorder10.1038/s41598-021-94122-72045-2322https://doaj.org/article/79da7f272838489a822acb273f1d0efa2021-08-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-94122-7https://doaj.org/toc/2045-2322Abstract The pathogenesis of bipolar disorder (BD), a chronic mood disorder, is largely unknown. Noncoding RNAs play important roles in the pathogenesis of BD. However, little is known about the correlations of long noncoding RNAs (lncRNAs) with BD. Illumina high-throughput sequencing in BD patients and normal controls was used to identify differentially expressed (DE) genes. Two-step real-time quantitative reverse transcription polymerase chain reaction (qRT-PCR) was used to validate DE-RNAs in the first cohort (50 BD and 50 control subjects). Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways and lncRNA-mRNA coexpression and lncRNA-microRNA (miRNA)-messenger RNA (mRNA) competing endogenous RNA (ceRNA) network analyses were used to predict the functions of DE-RNAs. Receiver operating characteristic (ROC) curve analysis and logistic regression were applied to evaluate diagnostic performance in an additional testing group (80 BD and 66 control subjects). A total of 576 significantly DE-lncRNAs and 262 DE-mRNAs were identified in BD patients, and 95 lncRNA-miRNA-mRNA interactions were used to construct a ceRNA regulatory network. Analysis of the first cohort showed that six RNAs (NR_028138.1, TCONS_00018621, TCONS_00002186, TNF, PID1, and SDK1) were differentially expressed in the BD group (P < 0.01). NR_028138.1 was used to establish a BD diagnostic model (area under the ROC curve 0.923, P < 0.004, 95% CI: 0.830–0.999). Verification in the second cohort revealed uniformly significant differences in NR_028138.1 (P < 0.0001). This study constructed a ceRNA regulatory network and provided a hypothesis for the pathogenesis of BD. NR_028138.1 was identified as a central element involved in the transcriptional regulation in BD and a potential biomarker.Ling HePengtao ZouWanlei SunYonghui FuWenfeng HeJuxiang LiNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-11 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Ling He
Pengtao Zou
Wanlei Sun
Yonghui Fu
Wenfeng He
Juxiang Li
Identification of lncRNA NR_028138.1 as a biomarker and construction of a ceRNA network for bipolar disorder
description Abstract The pathogenesis of bipolar disorder (BD), a chronic mood disorder, is largely unknown. Noncoding RNAs play important roles in the pathogenesis of BD. However, little is known about the correlations of long noncoding RNAs (lncRNAs) with BD. Illumina high-throughput sequencing in BD patients and normal controls was used to identify differentially expressed (DE) genes. Two-step real-time quantitative reverse transcription polymerase chain reaction (qRT-PCR) was used to validate DE-RNAs in the first cohort (50 BD and 50 control subjects). Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways and lncRNA-mRNA coexpression and lncRNA-microRNA (miRNA)-messenger RNA (mRNA) competing endogenous RNA (ceRNA) network analyses were used to predict the functions of DE-RNAs. Receiver operating characteristic (ROC) curve analysis and logistic regression were applied to evaluate diagnostic performance in an additional testing group (80 BD and 66 control subjects). A total of 576 significantly DE-lncRNAs and 262 DE-mRNAs were identified in BD patients, and 95 lncRNA-miRNA-mRNA interactions were used to construct a ceRNA regulatory network. Analysis of the first cohort showed that six RNAs (NR_028138.1, TCONS_00018621, TCONS_00002186, TNF, PID1, and SDK1) were differentially expressed in the BD group (P < 0.01). NR_028138.1 was used to establish a BD diagnostic model (area under the ROC curve 0.923, P < 0.004, 95% CI: 0.830–0.999). Verification in the second cohort revealed uniformly significant differences in NR_028138.1 (P < 0.0001). This study constructed a ceRNA regulatory network and provided a hypothesis for the pathogenesis of BD. NR_028138.1 was identified as a central element involved in the transcriptional regulation in BD and a potential biomarker.
format article
author Ling He
Pengtao Zou
Wanlei Sun
Yonghui Fu
Wenfeng He
Juxiang Li
author_facet Ling He
Pengtao Zou
Wanlei Sun
Yonghui Fu
Wenfeng He
Juxiang Li
author_sort Ling He
title Identification of lncRNA NR_028138.1 as a biomarker and construction of a ceRNA network for bipolar disorder
title_short Identification of lncRNA NR_028138.1 as a biomarker and construction of a ceRNA network for bipolar disorder
title_full Identification of lncRNA NR_028138.1 as a biomarker and construction of a ceRNA network for bipolar disorder
title_fullStr Identification of lncRNA NR_028138.1 as a biomarker and construction of a ceRNA network for bipolar disorder
title_full_unstemmed Identification of lncRNA NR_028138.1 as a biomarker and construction of a ceRNA network for bipolar disorder
title_sort identification of lncrna nr_028138.1 as a biomarker and construction of a cerna network for bipolar disorder
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/79da7f272838489a822acb273f1d0efa
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