High-throughput screening of glucocorticoid-induced enhancer activity reveals mechanisms of stress-related psychiatric disorders
Exposure to stressful life events increases the risk for psychiatric disorders. Mechanistic insight into the genetic factors moderating the impact of stress can increase our understanding of disease processes. Here, we test 3,662 single nucleotide polymorphisms (SNPs) from preselected expression qua...
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Veröffentlicht in: | Proceedings of the National Academy of Sciences - PNAS 2023-12, Vol.120 (49), p.e2305773120-e2305773120 |
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creator | Penner-Goeke, Signe Bothe, Melissa Rek, Nils Kreitmaier, Peter Pöhlchen, Dorothee Kühnel, Anne Glaser, Laura V Kaya, Ezgi Krontira, Anthi C Röh, Simone Czamara, Darina Ködel, Maik Monteserin-Garcia, Jose Diener, Laura Wölfel, Barbara Sauer, Susann Rummel, Christine Riesenberg, Stephan Arloth-Knauer, Janine Ziller, Michael Labeur, Marta Meijsing, Sebastiaan Binder, Elisabeth B |
description | Exposure to stressful life events increases the risk for psychiatric disorders. Mechanistic insight into the genetic factors moderating the impact of stress can increase our understanding of disease processes. Here, we test 3,662 single nucleotide polymorphisms (SNPs) from preselected expression quantitative trait loci in massively parallel reporter assays to identify genetic variants that modulate the activity of regulatory elements sensitive to glucocorticoids, important mediators of the stress response. Of the tested SNP sequences, 547 were located in glucocorticoid-responsive regulatory elements of which 233 showed allele-dependent activity. Transcripts regulated by these functional variants were enriched for those differentially expressed in psychiatric disorders in the postmortem brain. Phenome-wide Mendelian randomization analysis in 4,439 phenotypes revealed potentially causal associations specifically in neurobehavioral traits, including major depression and other psychiatric disorders. Finally, a functional gene score derived from these variants was significantly associated with differences in the physiological stress response, suggesting that these variants may alter disease risk by moderating the individual set point of the stress response. |
doi_str_mv | 10.1073/pnas.2305773120 |
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Mechanistic insight into the genetic factors moderating the impact of stress can increase our understanding of disease processes. Here, we test 3,662 single nucleotide polymorphisms (SNPs) from preselected expression quantitative trait loci in massively parallel reporter assays to identify genetic variants that modulate the activity of regulatory elements sensitive to glucocorticoids, important mediators of the stress response. Of the tested SNP sequences, 547 were located in glucocorticoid-responsive regulatory elements of which 233 showed allele-dependent activity. Transcripts regulated by these functional variants were enriched for those differentially expressed in psychiatric disorders in the postmortem brain. Phenome-wide Mendelian randomization analysis in 4,439 phenotypes revealed potentially causal associations specifically in neurobehavioral traits, including major depression and other psychiatric disorders. Finally, a functional gene score derived from these variants was significantly associated with differences in the physiological stress response, suggesting that these variants may alter disease risk by moderating the individual set point of the stress response.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.2305773120</identifier><identifier>PMID: 38011552</identifier><language>eng</language><publisher>United States: National Academy of Sciences</publisher><subject>Biological Sciences ; Disorders ; Gene mapping ; Genetic diversity ; Genetic factors ; Genetic Predisposition to Disease ; Genetic variance ; Genome-Wide Association Study ; Glucocorticoids ; Health risks ; High-throughput screening ; High-Throughput Screening Assays ; Humans ; Mental disorders ; Mental Disorders - genetics ; Nucleotides ; Phenotypes ; Polymorphism, Single Nucleotide ; Quantitative Trait Loci ; Regulatory sequences ; Regulatory Sequences, Nucleic Acid ; Single-nucleotide polymorphism ; Stress (physiology) ; Stress response</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 2023-12, Vol.120 (49), p.e2305773120-e2305773120</ispartof><rights>Copyright National Academy of Sciences Dec 5, 2023</rights><rights>Copyright © 2023 the Author(s). 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Mechanistic insight into the genetic factors moderating the impact of stress can increase our understanding of disease processes. Here, we test 3,662 single nucleotide polymorphisms (SNPs) from preselected expression quantitative trait loci in massively parallel reporter assays to identify genetic variants that modulate the activity of regulatory elements sensitive to glucocorticoids, important mediators of the stress response. Of the tested SNP sequences, 547 were located in glucocorticoid-responsive regulatory elements of which 233 showed allele-dependent activity. Transcripts regulated by these functional variants were enriched for those differentially expressed in psychiatric disorders in the postmortem brain. Phenome-wide Mendelian randomization analysis in 4,439 phenotypes revealed potentially causal associations specifically in neurobehavioral traits, including major depression and other psychiatric disorders. 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subjects | Biological Sciences Disorders Gene mapping Genetic diversity Genetic factors Genetic Predisposition to Disease Genetic variance Genome-Wide Association Study Glucocorticoids Health risks High-throughput screening High-Throughput Screening Assays Humans Mental disorders Mental Disorders - genetics Nucleotides Phenotypes Polymorphism, Single Nucleotide Quantitative Trait Loci Regulatory sequences Regulatory Sequences, Nucleic Acid Single-nucleotide polymorphism Stress (physiology) Stress response |
title | High-throughput screening of glucocorticoid-induced enhancer activity reveals mechanisms of stress-related psychiatric disorders |
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