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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...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2018
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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. |
format | Online Article Text |
id | pubmed-6069762 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
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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