The role of m6A/m-RNA methylation in stress response regulation

M Engel, C Eggert, PM Kaplick, M Eder, S Röh, L Tietze… - Neuron, 2018 - cell.com
M Engel, C Eggert, PM Kaplick, M Eder, S Röh, L Tietze, C Namendorf, J Arloth, P Weber…
Neuron, 2018cell.com
Summary 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 …
Summary
N6-methyladenosine (m6A) and N6,2′-O-dimethyladenosine (m6Am) are abundant mRNA modifications that regulate transcript processing and translation. The role of both, here termed m6A/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 m6A/m-seq, global and gene-specific m6A/m measurements. We show that stress exposure and glucocorticoids region and time specifically alter m6A/m and its regulatory network. We demonstrate that deletion of the methyltransferase Mettl3 or the demethylase Fto in adult neurons alters the m6A/m epitranscriptome, increases fear memory, and changes the transcriptome response to fear and synaptic plasticity. Moreover, we report that regulation of m6A/m is impaired in major depressive disorder patients following glucocorticoid stimulation. Our findings indicate that brain m6A/m represents a novel layer of complexity in gene expression regulation after stress and that dysregulation of the m6A/m response may contribute to the pathophysiology of stress-related psychiatric disorders.
cell.com
以上显示的是最相近的搜索结果。 查看全部搜索结果