RT Journal Article
SR Electronic
T1 The role of m6A-RNA methylation in stress response regulation
JF bioRxiv
FD Cold Spring Harbor Laboratory
SP 200402
DO 10.1101/200402
A1 Mareen Engel
A1 Simone Röh
A1 Carola Eggert
A1 Paul M. Kaplick
A1 Lisa Tietze
A1 Janine Arloth
A1 Peter Weber
A1 Monika Rex-Haffner
A1 Mira Jakovcevski
A1 Manfred Uhr
A1 Matthias Eder
A1 Carsten T. Wotjak
A1 Mathias V. Schmidt
A1 Jan M. Deussing
A1 Elisabeth B. Binder
A1 Alon Chen
YR 2017
UL http://biorxiv.org/content/early/2017/11/12/200402.abstract
AB N6-Methyladenosine (m6A) is an abundant internal RNA modification that regulates transcript processing and translation. The regulation of brain m6A by stressful stimuli in vivo and its role in the stress response are currently unknown.Here, we provide a detailed analysis of the stress-epitranscriptome using m6A-Seq, global and gene-specific m6A measurements. We show that stress exposure and glucocorticoids alter m6A and its regulatory network in a region- and time-specific manner. We demonstrate that depletion of the methyltransferase Mettl3 and the demethylase Fto in adult neurons increases fear memory, and alters the transcriptome response to fear as well as synaptic plasticity. Finally, we report that regulation of m6A is impaired in major depressive disorder patients following glucocorticoid receptor activation.Our findings indicate that brain m6A represents a novel layer of complexity in gene expression regulation after stress and that dysregulation of the m6A-response may contribute to the pathophysiology of stress-related psychiatric disorders.Highlightsm6A RNA methylation in adult mouse brain is regulated by stressBrain m6A levels are temporally and spatially regulated by stressMettl3 and Fto-KO alter fear memory, transcriptome response and synaptic plasticityThe m6A-glucocorticoid-response is impaired in major depressive disorder patientseTOC blurb Engel et al. demonstrate a brain-area-specific and time-dependent role for the mRNA modification, m6A, in stress-response regulation. Manipulating m6A-enzymes alters fear-memory, transcriptome-response and synaptic-plasticity. Altered m6A dynamics in depressed patients suggest an involvement of m6A-modifications in stress-related psychiatric disorders.