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The Role of m 6 A/m-RNA Methylation in Stress Response Regulation.

Authors :
Engel M
Eggert C
Kaplick PM
Eder M
Röh S
Tietze L
Namendorf C
Arloth J
Weber P
Rex-Haffner M
Geula S
Jakovcevski M
Hanna JH
Leshkowitz D
Uhr M
Wotjak CT
Schmidt MV
Deussing JM
Binder EB
Chen A
Source :
Neuron [Neuron] 2018 Jul 25; Vol. 99 (2), pp. 389-403.e9.
Publication Year :
2018

Abstract

N <superscript>6</superscript> -methyladenosine (m <superscript>6</superscript> A) and N <superscript>6</superscript> ,2'-O-dimethyladenosine (m <superscript>6</superscript> Am) are abundant mRNA modifications that regulate transcript processing and translation. The role of both, here termed m <superscript>6</superscript> A/m, in the stress response in the adult brain in vivo is currently unknown. Here, we provide a detailed analysis of the stress epitranscriptome using m <superscript>6</superscript> A/m-seq, global and gene-specific m <superscript>6</superscript> A/m measurements. We show that stress exposure and glucocorticoids region and time specifically alter m <superscript>6</superscript> A/m and its regulatory network. We demonstrate that deletion of the methyltransferase Mettl3 or the demethylase Fto in adult neurons alters the m <superscript>6</superscript> A/m epitranscriptome, increases fear memory, and changes the transcriptome response to fear and synaptic plasticity. Moreover, we report that regulation of m <superscript>6</superscript> A/m is impaired in major depressive disorder patients following glucocorticoid stimulation. Our findings indicate that brain m <superscript>6</superscript> A/m represents a novel layer of complexity in gene expression regulation after stress and that dysregulation of the m <superscript>6</superscript> A/m response may contribute to the pathophysiology of stress-related psychiatric disorders.<br /> (Copyright © 2018 The Author(s). Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1097-4199
Volume :
99
Issue :
2
Database :
MEDLINE
Journal :
Neuron
Publication Type :
Academic Journal
Accession number :
30048615
Full Text :
https://doi.org/10.1016/j.neuron.2018.07.009