Genetic Differences in the Immediate Transcriptome Response to Stress Predict Risk-Related Brain Function and Psychiatric Disorders

Janine Arloth(Max Planck Institute of Psychiatry), Ryan Bogdan(Washington University in St. Louis), Peter Weber(Max Planck Institute of Psychiatry), Goar Frishman(Helmholtz Zentrum München), Andreas Menke(Max Planck Institute of Psychiatry), Klaus V. Wagner(Max Planck Institute of Psychiatry), Georgia Balsevich(Max Planck Institute of Psychiatry), Mathias V. Schmidt(Max Planck Institute of Psychiatry), Nazanin Karbalai(Max Planck Institute of Psychiatry), Darina Czamara(Max Planck Institute of Psychiatry), André Altmann(Stanford University), Dietrich Trümbach(Helmholtz Zentrum München), Wolfgang Wurst(German Center for Neurodegenerative Diseases), Divya Mehta(Max Planck Institute of Psychiatry), Manfred Uhr(Max Planck Institute of Psychiatry), Torsten Klengel(Max Planck Institute of Psychiatry), Angelika Erhardt(Max Planck Institute of Psychiatry), Caitlin E. Carey(Washington University in St. Louis), Emily Drabant Conley(23andMe (United States)), Andreas Ruepp(Helmholtz Zentrum München), Bertram Müller-Myhsok(University of Liverpool), Ahmad R. Hariri(Duke University), Elisabeth B. Binder(Emory University), Stephan Ripke, Naomi R. Wray, Cathryn M. Lewis, Steven P. Hamilton, Myrna M. Weissman, Gerome Breen, Enda M. Byrne, Douglas Blackwood, Dorret I. Boomsma, Sven Cichon, Andrew C. Heath, Florian Holsboer, Susanne Lucae, Pamela A. F. Madden, Nicholas G. Martin, Peter McGuffin(Max Planck Institute of Psychiatry), Pierandrea Muglia, Markus M. Nöethen, Brenda P. Penninx, Michele L. Pergadia, James B. Potash, Marcella Rietschel, D. Y. Lin(Washington University in St. Louis), Bertram Müller-Myhsok(University of Liverpool), Jianxin Shi, Stacy Steinberg, Hans J. Grabe, Paul Lichtenstein, Patrik K. E. Magnusson, Roy H. Perlis, Martin Preisig, Jordan W. Smoller, Kāri Stefánsson, Rudolf Uher, Zoltán Kutalik, Katherine E. Tansey, Alexander Teumer, Alexander Viktorin, Michael R. Barnes, Thomas Bettecken, Elisabeth B. Binder(Emory University), René Breuer, Víctor M. Castro, Susanne Churchill, William Coryell, Nick Craddock, Ian Craig, Darina Czamara(Max Planck Institute of Psychiatry), Eco J. C. de Geus, Franziska Degenhardt, Anne Farmer, Maurizio Fava, Josef Frank, Vivian S. Gainer, Patience Gallagher, Scott D. Gordon, Sergey Goryachev, Magdalena Groß, Michel Guipponi, Anjali K. Henders, Stefan Herms, Ian B. Hickie, Susanne Hoefels, Witte J.G. Hoogendijk, Jouke Jan Hottenga, Dan V. Iosifescu, Marcus Ising, Ian Jones, Lisa Jones(Emory University), Tzeng Jung-Ying, James A. Knowles, Isaac S. Kohane, Martin Kohli, Ania Korszun, Mikael Landén, William Lawson, Glyn Lewis, Donald J. MacIntyre, Wolfgang Maier(German Center for Neurodegenerative Diseases), Manuel Mattheisen, Patrick J. McGrath, Andrew M. McIntosh, Alan McLean, Christel M. Middeldorp, Lefkos Middleton, Grant M. Montgomery, Shawn N. Murphy, Matthias Nauck, Willem A. Nolen, Dale R. Nyholt, Michael O‘Donovan, Högni Óskarsson, Nancy L. Pedersen, William A. Scheftner, Andrea Schulz(Helmholtz Zentrum München), Thomas G. Schulze, Stanley I. Shyn, Engilbert Sigurðsson, Susan L. Slager, Johannes H. Smit, Hreinn Stefánsson, Michael Steffens, Thorgeir E. Thorgeirsson, Federica Tozzi, Jens Treutlein, Manfred Uhr(Max Planck Institute of Psychiatry), Edwin J.C.G. van den Oord, Gerard van Grootheest, Henry Völzke, Jeffrey B. Weilburg, Gonneke Willemsen, Frans G. Zitman, Benjamin M. Neale, Mark J. Daly, Douglas F. Levinson, Patrick F. Sullivan
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Abstract

Depression risk is exacerbated by genetic factors and stress exposure; however, the biological mechanisms through which these factors interact to confer depression risk are poorly understood. One putative biological mechanism implicates variability in the ability of cortisol, released in response to stress, to trigger a cascade of adaptive genomic and non-genomic processes through glucocorticoid receptor (GR) activation. Here, we demonstrate that common genetic variants in long-range enhancer elements modulate the immediate transcriptional response to GR activation in human blood cells. These functional genetic variants increase risk for depression and co-heritable psychiatric disorders. Moreover, these risk variants are associated with inappropriate amygdala reactivity, a transdiagnostic psychiatric endophenotype and an important stress hormone response trigger. Network modeling and animal experiments suggest that these genetic differences in GR-induced transcriptional activation may mediate the risk for depression and other psychiatric disorders by altering a network of functionally related stress-sensitive genes in blood and brain.Video AbstracteyJraWQiOiI4ZjUxYWNhY2IzYjhiNjNlNzFlYmIzYWFmYTU5NmZmYyIsImFsZyI6IlJTMjU2In0.eyJzdWIiOiIzMzZiNzBlYmUwOTU5OTJiYjdmMDdkNDI5MjAyY2U0ZSIsImtpZCI6IjhmNTFhY2FjYjNiOGI2M2U3MWViYjNhYWZhNTk2ZmZjIiwiZXhwIjoxNjc3ODgzNjMyfQ.daHoxICTwrJX6ZeOQWpRUM71xBa_mLjLLmVAYHu42j1WPhZ8S7A7EgEwNg54kK7QYxKnrZxM5ZqZJKOGzKmbgcwoozh_bNz7Yy8RmvLw3-6TT8KMI2ainTKmcRLT-ziLex0TkKA-poSD3IMyPqTrZDSWI-nVZONJK7f6I3yfdSkSbMowhOOuOJTbRSNUvSvmN-O0qKZ0Bk3W0TJo_lspNrAS5LYCYS07sDDnTcsMvgi8xC-9ogtTJI-lLegWo9rh4QP50lbLSMCT_6Yuif0sHlLOAPwWCuMozIm5v7VXgEHOwDmG9_8GlbhoDQAGZmqgRZyAfz9kMb_mvkKMcsVYQg(mp4, (73.08 MB) Download video


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