High-throughput screening of glucocorticoid-induced enhancer activity reveals mechanisms of stress-related psychiatric disorders

Author:

Penner-Goeke Signe12,Bothe Melissa3,Rek Nils14ORCID,Kreitmaier Peter5,Pöhlchen Dorothee14,Kühnel Anne14ORCID,Glaser Laura V.3ORCID,Kaya Ezgi12,Krontira Anthi C.14ORCID,Röh Simone1ORCID,Czamara Darina1ORCID,Ködel Maik1,Monteserin-Garcia Jose1ORCID,Diener Laura1,Wölfel Barbara1,Sauer Susann1,Rummel Christine1ORCID,Riesenberg Stephan6ORCID,Arloth-Knauer Janine1ORCID,Ziller Michael17,Labeur Marta1,Meijsing Sebastiaan3,Binder Elisabeth B.1ORCID

Affiliation:

1. Department of Translational Research in Psychiatry, Max Planck Institute of Psychiatry, Munich 80804, Germany

2. Graduate School of Systemic Neurosciences, Ludwig Maximilian University of Munich, Planegg 82152, Germany

3. Department of Computational Molecular Biology, Max Planck Institute of Molecular Genetics, Berlin 14195, Germany

4. International Max Planck Research School for Translational Psychiatry, Max Planck Institute of Psychiatry, Munich 80804, Germany

5. Institute of Translational Genomics, Helmholtz Munich, Neuherberg 85764, Germany

6. Department of Evolutionary Genetics, Max-Planck-Institute for Evolutionary Anthropology, Leipzig 04103, Germany

7. Department of Psychiatry, University of Muenster, Muenster 48149, Germany

Abstract

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.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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