4.8 Article

The Role of m6A/m-RNA Methylation in Stress Response Regulation

期刊

NEURON
卷 99, 期 2, 页码 389-+

出版社

CELL PRESS
DOI: 10.1016/j.neuron.2018.07.009

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资金

  1. Boehringer Ingelheim Fonds
  2. European Research Council (FP7 grant) [260463]
  3. Israel Science Foundation [1565/15, 1916/12, 355/17, 107/14]
  4. ERANET Program
  5. Chief Scientist Office of the Israeli Ministry of Health [3-11389]
  6. Federal Ministry of Education and Research [01KU1501A]
  7. I-CORE Program of the Planning and Budgeting Committee
  8. Nella and Leon Benoziyo Center for Neurological Diseases
  9. Henry Chanoch Krenter Institute for Biomedical Imaging and Genomics
  10. Perlman Family Foundation
  11. Adelis Foundation
  12. Irving I. Moskowitz Foundation
  13. FAMRI grant
  14. NYSCF grant
  15. European Research Council (ERC) [260463] Funding Source: European Research Council (ERC)

向作者/读者索取更多资源

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 stressrelated psychiatric disorders.

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