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Transcriptome-Wide Association Study Provides Insights Into the Genetic Component of Gene Expression in Anxiety
Anxiety disorders are common mental disorders that often result in disability. Recently, large-scale genome-wide association studies (GWASs) have identified several novel risk variants and loci for anxiety disorders (or anxiety traits). Nevertheless, how the reported risk variants confer risk of anx...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8505959/ https://www.ncbi.nlm.nih.gov/pubmed/34650599 http://dx.doi.org/10.3389/fgene.2021.740134 |
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author | Su, Xi Li, Wenqiang Lv, Luxian Li, Xiaoyan Yang, Jinfeng Luo, Xiong-Jian Liu, Jiewei |
author_facet | Su, Xi Li, Wenqiang Lv, Luxian Li, Xiaoyan Yang, Jinfeng Luo, Xiong-Jian Liu, Jiewei |
author_sort | Su, Xi |
collection | PubMed |
description | Anxiety disorders are common mental disorders that often result in disability. Recently, large-scale genome-wide association studies (GWASs) have identified several novel risk variants and loci for anxiety disorders (or anxiety traits). Nevertheless, how the reported risk variants confer risk of anxiety remains unknown. To identify genes whose cis-regulated expression levels are associated with risk of anxiety traits, we conducted a transcriptome-wide association study (TWAS) by integrating genome-wide associations from a large-scale GWAS (N = 175,163) (which evaluated anxiety traits based on Generalized Anxiety Disorder 2-item scale (GAD-2) score) and brain expression quantitative trait loci (eQTL) data (from the PsychENCODE and GTEx). We identified 19 and 17 transcriptome-wide significant (TWS) genes in the PsychENCODE and GTEx, respectively. Intriguingly, 10 genes showed significant associations with anxiety in both datasets, strongly suggesting that genetic risk variants may confer risk of anxiety traits by regulating the expression of these genes. Top TWS genes included RNF123, KANSL1-AS1, GLYCTK, CRHR1, DND1P1, MAPT and ARHGAP27. Of note, 25 TWS genes were not implicated in the original GWAS. Our TWAS identified 26 risk genes whose cis-regulated expression were significantly associated with anxiety, providing important insights into the genetic component of gene expression in anxiety disorders/traits and new clues for future drug development. |
format | Online Article Text |
id | pubmed-8505959 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-85059592021-10-13 Transcriptome-Wide Association Study Provides Insights Into the Genetic Component of Gene Expression in Anxiety Su, Xi Li, Wenqiang Lv, Luxian Li, Xiaoyan Yang, Jinfeng Luo, Xiong-Jian Liu, Jiewei Front Genet Genetics Anxiety disorders are common mental disorders that often result in disability. Recently, large-scale genome-wide association studies (GWASs) have identified several novel risk variants and loci for anxiety disorders (or anxiety traits). Nevertheless, how the reported risk variants confer risk of anxiety remains unknown. To identify genes whose cis-regulated expression levels are associated with risk of anxiety traits, we conducted a transcriptome-wide association study (TWAS) by integrating genome-wide associations from a large-scale GWAS (N = 175,163) (which evaluated anxiety traits based on Generalized Anxiety Disorder 2-item scale (GAD-2) score) and brain expression quantitative trait loci (eQTL) data (from the PsychENCODE and GTEx). We identified 19 and 17 transcriptome-wide significant (TWS) genes in the PsychENCODE and GTEx, respectively. Intriguingly, 10 genes showed significant associations with anxiety in both datasets, strongly suggesting that genetic risk variants may confer risk of anxiety traits by regulating the expression of these genes. Top TWS genes included RNF123, KANSL1-AS1, GLYCTK, CRHR1, DND1P1, MAPT and ARHGAP27. Of note, 25 TWS genes were not implicated in the original GWAS. Our TWAS identified 26 risk genes whose cis-regulated expression were significantly associated with anxiety, providing important insights into the genetic component of gene expression in anxiety disorders/traits and new clues for future drug development. Frontiers Media S.A. 2021-09-28 /pmc/articles/PMC8505959/ /pubmed/34650599 http://dx.doi.org/10.3389/fgene.2021.740134 Text en Copyright © 2021 Su, Li, Lv, Li, Yang, Luo and Liu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Genetics Su, Xi Li, Wenqiang Lv, Luxian Li, Xiaoyan Yang, Jinfeng Luo, Xiong-Jian Liu, Jiewei Transcriptome-Wide Association Study Provides Insights Into the Genetic Component of Gene Expression in Anxiety |
title | Transcriptome-Wide Association Study Provides Insights Into the Genetic Component of Gene Expression in Anxiety |
title_full | Transcriptome-Wide Association Study Provides Insights Into the Genetic Component of Gene Expression in Anxiety |
title_fullStr | Transcriptome-Wide Association Study Provides Insights Into the Genetic Component of Gene Expression in Anxiety |
title_full_unstemmed | Transcriptome-Wide Association Study Provides Insights Into the Genetic Component of Gene Expression in Anxiety |
title_short | Transcriptome-Wide Association Study Provides Insights Into the Genetic Component of Gene Expression in Anxiety |
title_sort | transcriptome-wide association study provides insights into the genetic component of gene expression in anxiety |
topic | Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8505959/ https://www.ncbi.nlm.nih.gov/pubmed/34650599 http://dx.doi.org/10.3389/fgene.2021.740134 |
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