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

N(6)-methyladenosine (m(6)A) and N(6),2′-O-dimethyladenosine (m(6)Am) are abundant mRNA modifications that regulate transcript processing and translation. The role of both, here termed m(6)A/m, in the stress response in the adult brain in vivo is currently unknown. Here, we provide a detailed analys...

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Autores principales: Engel, Mareen, Eggert, Carola, Kaplick, Paul M., Eder, Matthias, Röh, Simone, Tietze, Lisa, Namendorf, Christian, Arloth, Janine, Weber, Peter, Rex-Haffner, Monika, Geula, Shay, Jakovcevski, Mira, Hanna, Jacob H., Leshkowitz, Dena, Uhr, Manfred, Wotjak, Carsten T., Schmidt, Mathias V., Deussing, Jan M., Binder, Elisabeth B., Chen, Alon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6069762/
https://www.ncbi.nlm.nih.gov/pubmed/30048615
http://dx.doi.org/10.1016/j.neuron.2018.07.009
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author Engel, Mareen
Eggert, Carola
Kaplick, Paul M.
Eder, Matthias
Röh, Simone
Tietze, Lisa
Namendorf, Christian
Arloth, Janine
Weber, Peter
Rex-Haffner, Monika
Geula, Shay
Jakovcevski, Mira
Hanna, Jacob H.
Leshkowitz, Dena
Uhr, Manfred
Wotjak, Carsten T.
Schmidt, Mathias V.
Deussing, Jan M.
Binder, Elisabeth B.
Chen, Alon
author_facet Engel, Mareen
Eggert, Carola
Kaplick, Paul M.
Eder, Matthias
Röh, Simone
Tietze, Lisa
Namendorf, Christian
Arloth, Janine
Weber, Peter
Rex-Haffner, Monika
Geula, Shay
Jakovcevski, Mira
Hanna, Jacob H.
Leshkowitz, Dena
Uhr, Manfred
Wotjak, Carsten T.
Schmidt, Mathias V.
Deussing, Jan M.
Binder, Elisabeth B.
Chen, Alon
author_sort Engel, Mareen
collection PubMed
description N(6)-methyladenosine (m(6)A) and N(6),2′-O-dimethyladenosine (m(6)Am) are abundant mRNA modifications that regulate transcript processing and translation. The role of both, here termed m(6)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(6)A/m-seq, global and gene-specific m(6)A/m measurements. We show that stress exposure and glucocorticoids region and time specifically alter m(6)A/m and its regulatory network. We demonstrate that deletion of the methyltransferase Mettl3 or the demethylase Fto in adult neurons alters the m(6)A/m epitranscriptome, increases fear memory, and changes the transcriptome response to fear and synaptic plasticity. Moreover, we report that regulation of m(6)A/m is impaired in major depressive disorder patients following glucocorticoid stimulation. Our findings indicate that brain m(6)A/m represents a novel layer of complexity in gene expression regulation after stress and that dysregulation of the m(6)A/m response may contribute to the pathophysiology of stress-related psychiatric disorders.
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spelling pubmed-60697622018-08-01 The Role of m(6)A/m-RNA Methylation in Stress Response Regulation Engel, Mareen Eggert, Carola Kaplick, Paul M. Eder, Matthias Röh, Simone Tietze, Lisa Namendorf, Christian Arloth, Janine Weber, Peter Rex-Haffner, Monika Geula, Shay Jakovcevski, Mira Hanna, Jacob H. Leshkowitz, Dena Uhr, Manfred Wotjak, Carsten T. Schmidt, Mathias V. Deussing, Jan M. Binder, Elisabeth B. Chen, Alon Neuron Article N(6)-methyladenosine (m(6)A) and N(6),2′-O-dimethyladenosine (m(6)Am) are abundant mRNA modifications that regulate transcript processing and translation. The role of both, here termed m(6)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(6)A/m-seq, global and gene-specific m(6)A/m measurements. We show that stress exposure and glucocorticoids region and time specifically alter m(6)A/m and its regulatory network. We demonstrate that deletion of the methyltransferase Mettl3 or the demethylase Fto in adult neurons alters the m(6)A/m epitranscriptome, increases fear memory, and changes the transcriptome response to fear and synaptic plasticity. Moreover, we report that regulation of m(6)A/m is impaired in major depressive disorder patients following glucocorticoid stimulation. Our findings indicate that brain m(6)A/m represents a novel layer of complexity in gene expression regulation after stress and that dysregulation of the m(6)A/m response may contribute to the pathophysiology of stress-related psychiatric disorders. Cell Press 2018-07-25 /pmc/articles/PMC6069762/ /pubmed/30048615 http://dx.doi.org/10.1016/j.neuron.2018.07.009 Text en © 2018 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Engel, Mareen
Eggert, Carola
Kaplick, Paul M.
Eder, Matthias
Röh, Simone
Tietze, Lisa
Namendorf, Christian
Arloth, Janine
Weber, Peter
Rex-Haffner, Monika
Geula, Shay
Jakovcevski, Mira
Hanna, Jacob H.
Leshkowitz, Dena
Uhr, Manfred
Wotjak, Carsten T.
Schmidt, Mathias V.
Deussing, Jan M.
Binder, Elisabeth B.
Chen, Alon
The Role of m(6)A/m-RNA Methylation in Stress Response Regulation
title The Role of m(6)A/m-RNA Methylation in Stress Response Regulation
title_full The Role of m(6)A/m-RNA Methylation in Stress Response Regulation
title_fullStr The Role of m(6)A/m-RNA Methylation in Stress Response Regulation
title_full_unstemmed The Role of m(6)A/m-RNA Methylation in Stress Response Regulation
title_short The Role of m(6)A/m-RNA Methylation in Stress Response Regulation
title_sort role of m(6)a/m-rna methylation in stress response regulation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6069762/
https://www.ncbi.nlm.nih.gov/pubmed/30048615
http://dx.doi.org/10.1016/j.neuron.2018.07.009
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