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Global long non-coding RNA expression in the rostral anterior cingulate cortex of depressed suicides

Long non-coding RNAs (lncRNAs) are an emerging class of regulatory RNA that may be implicated in psychiatric disorders. Here we performed RNA-sequencing in the rostral anterior cingulate cortex of 26 depressed suicides and 24 matched controls. We first performed differential lncRNA expression analys...

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Autores principales: Zhou, Yi, Lutz, Pierre-Eric, Wang, Yu Chang, Ragoussis, Jiannis, Turecki, Gustavo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6193959/
https://www.ncbi.nlm.nih.gov/pubmed/30337518
http://dx.doi.org/10.1038/s41398-018-0267-7
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author Zhou, Yi
Lutz, Pierre-Eric
Wang, Yu Chang
Ragoussis, Jiannis
Turecki, Gustavo
author_facet Zhou, Yi
Lutz, Pierre-Eric
Wang, Yu Chang
Ragoussis, Jiannis
Turecki, Gustavo
author_sort Zhou, Yi
collection PubMed
description Long non-coding RNAs (lncRNAs) are an emerging class of regulatory RNA that may be implicated in psychiatric disorders. Here we performed RNA-sequencing in the rostral anterior cingulate cortex of 26 depressed suicides and 24 matched controls. We first performed differential lncRNA expression analysis, and then conducted Weighted Gene Co-expression Network Analysis (WGCNA) to identify co-expression modules associating with depression and suicide. We identified 23 differentially expressed lncRNAs (FDR < 0.1) as well as their differentially expressed overlapping and antisense protein-coding genes. Several of these overlapping or antisense genes were associated with interferon signaling, which is a component of the innate immune response. Using WGCNA, we identified modules of highly co-expressed genes associated with depression and suicide and found protein-coding genes highly connected to differentially expressed lncRNAs within these modules. These protein-coding genes were located distal to their associated lncRNAs and were found to be part of several GO terms enriched in the significant modules, which include: cytoskeleton organization, plasma membrane, cell adhesion, nucleus, DNA-binding, and regulation of dendrite development and morphology. Altogether, we report that lncRNAs are differentially expressed in the brains of depressed individuals who died by suicide and may represent regulators of important molecular functions and biological processes.
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spelling pubmed-61939592018-10-19 Global long non-coding RNA expression in the rostral anterior cingulate cortex of depressed suicides Zhou, Yi Lutz, Pierre-Eric Wang, Yu Chang Ragoussis, Jiannis Turecki, Gustavo Transl Psychiatry Article Long non-coding RNAs (lncRNAs) are an emerging class of regulatory RNA that may be implicated in psychiatric disorders. Here we performed RNA-sequencing in the rostral anterior cingulate cortex of 26 depressed suicides and 24 matched controls. We first performed differential lncRNA expression analysis, and then conducted Weighted Gene Co-expression Network Analysis (WGCNA) to identify co-expression modules associating with depression and suicide. We identified 23 differentially expressed lncRNAs (FDR < 0.1) as well as their differentially expressed overlapping and antisense protein-coding genes. Several of these overlapping or antisense genes were associated with interferon signaling, which is a component of the innate immune response. Using WGCNA, we identified modules of highly co-expressed genes associated with depression and suicide and found protein-coding genes highly connected to differentially expressed lncRNAs within these modules. These protein-coding genes were located distal to their associated lncRNAs and were found to be part of several GO terms enriched in the significant modules, which include: cytoskeleton organization, plasma membrane, cell adhesion, nucleus, DNA-binding, and regulation of dendrite development and morphology. Altogether, we report that lncRNAs are differentially expressed in the brains of depressed individuals who died by suicide and may represent regulators of important molecular functions and biological processes. Nature Publishing Group UK 2018-10-18 /pmc/articles/PMC6193959/ /pubmed/30337518 http://dx.doi.org/10.1038/s41398-018-0267-7 Text en © The Author(s) 2018 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/.
spellingShingle Article
Zhou, Yi
Lutz, Pierre-Eric
Wang, Yu Chang
Ragoussis, Jiannis
Turecki, Gustavo
Global long non-coding RNA expression in the rostral anterior cingulate cortex of depressed suicides
title Global long non-coding RNA expression in the rostral anterior cingulate cortex of depressed suicides
title_full Global long non-coding RNA expression in the rostral anterior cingulate cortex of depressed suicides
title_fullStr Global long non-coding RNA expression in the rostral anterior cingulate cortex of depressed suicides
title_full_unstemmed Global long non-coding RNA expression in the rostral anterior cingulate cortex of depressed suicides
title_short Global long non-coding RNA expression in the rostral anterior cingulate cortex of depressed suicides
title_sort global long non-coding rna expression in the rostral anterior cingulate cortex of depressed suicides
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6193959/
https://www.ncbi.nlm.nih.gov/pubmed/30337518
http://dx.doi.org/10.1038/s41398-018-0267-7
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