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The DNA methyltransferase DNMT3A contributes to autophagy long-term memory

Macroautophagy/autophagy is a conserved catabolic pathway that targets cytoplasmic components for their degradation and recycling in an autophagosome-dependent lysosomal manner. Under physiological conditions, this process maintains cellular homeostasis. However, autophagy can be stimulated upon dif...

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Autores principales: González-Rodríguez, Patricia, Cheray, Mathilde, Füllgrabe, Jens, Salli, Maria, Engskog-Vlachos, Pinelopi, Keane, Lily, Cunha, Virginia, Lupa, Agata, Li, Wenbo, Ma, Qi, Dreij, Kristian, Rosenfeld, Michael G., Joseph, Bertrand
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8143216/
https://www.ncbi.nlm.nih.gov/pubmed/32876528
http://dx.doi.org/10.1080/15548627.2020.1816664
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author González-Rodríguez, Patricia
Cheray, Mathilde
Füllgrabe, Jens
Salli, Maria
Engskog-Vlachos, Pinelopi
Keane, Lily
Cunha, Virginia
Lupa, Agata
Li, Wenbo
Ma, Qi
Dreij, Kristian
Rosenfeld, Michael G.
Joseph, Bertrand
author_facet González-Rodríguez, Patricia
Cheray, Mathilde
Füllgrabe, Jens
Salli, Maria
Engskog-Vlachos, Pinelopi
Keane, Lily
Cunha, Virginia
Lupa, Agata
Li, Wenbo
Ma, Qi
Dreij, Kristian
Rosenfeld, Michael G.
Joseph, Bertrand
author_sort González-Rodríguez, Patricia
collection PubMed
description Macroautophagy/autophagy is a conserved catabolic pathway that targets cytoplasmic components for their degradation and recycling in an autophagosome-dependent lysosomal manner. Under physiological conditions, this process maintains cellular homeostasis. However, autophagy can be stimulated upon different forms of cellular stress, ranging from nutrient starvation to exposure to drugs. Thus, this pathway can be seen as a central component of the integrated and adaptive stress response. Here, we report that even brief induction of autophagy is coupled in vitro to a persistent downregulation of the expression of MAP1LC3 isoforms, which are key components of the autophagy core machinery. In fact, DNA-methylation mediated by de novo DNA methyltransferase DNMT3A of MAP1LC3 loci upon autophagy stimulation leads to the observed long-term decrease of MAP1LC3 isoforms at transcriptional level. Finally, we report that the downregulation of MAP1LC3 expression can be observed in vivo in zebrafish larvae and mice exposed to a transient autophagy stimulus. This epigenetic memory of autophagy provides some understanding of the long-term effect of autophagy induction and offers a possible mechanism for its decline upon aging, pathological conditions, or in response to treatment interventions. Abbreviations: ACTB: actin beta; ATG: autophagy-related; 5-Aza: 5-aza-2’-deoxycytidine; BafA1: bafilomycin A(1); CBZ: carbamazepine; CDKN2A: cyclin dependent kinase inhibitor 2A; ChIP: chromatin immunoprecipitation; Clon.: clonidine; CpG: cytosine-guanine dinucleotide: DMSO: dimethyl sulfoxide; DNA: deoxyribonucleic acid; DNMT: DNA methyltransferase; DNMT1: DNA methyltransferase 1; DNMT3A: DNA methyltransferase alpha; DNMT3B: DNA methyltransferase beta; dpf: days post-fertilization; EBSS: Earle’s balanced salt solution; EM: Zebrafish embryo medium; GABARAP: GABA type A receptor associated protein; GABARAPL1: GABA type A receptor associated protein like 1; GABARAPL2: GABA type A receptor associated protein like 2; GAPDH: glyceraldehyde-3-phosphate dehydrogenase; GRO-Seq: Global Run-On sequencing; MAP1LC3/LC3: microtubule-associated protein 1 light chain 3; MAP1LC3A: microtubule-associated protein 1 light chain 3 alpha; MAP1LC3B: microtubule-associated protein 1 light chain 3 beta; MAP1LC3B2: microtubule-associated protein 1 light chain 3 beta 2; MEM: minimum essential medium; MEF: mouse embryonic fibroblasts; mRNA: messenger RNA; MTOR: mechanistic target of rapamycin kinase; PBS: phosphate-buffered saline; PIK3C3: phosphatidylinositol 3-kinase catalytic subunit type 3; RB1CC1/FIP200: RB1 inducible coiled-coil 1; RT-qPCR: quantitative reverse transcription polymerase chain reaction; SQSTM1/p62: sequestosome 1; Starv.: starvation; Treh.: trehalose; ULK1: unc-51 like autophagy activating kinase 1.
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spelling pubmed-81432162021-06-07 The DNA methyltransferase DNMT3A contributes to autophagy long-term memory González-Rodríguez, Patricia Cheray, Mathilde Füllgrabe, Jens Salli, Maria Engskog-Vlachos, Pinelopi Keane, Lily Cunha, Virginia Lupa, Agata Li, Wenbo Ma, Qi Dreij, Kristian Rosenfeld, Michael G. Joseph, Bertrand Autophagy Research Paper Macroautophagy/autophagy is a conserved catabolic pathway that targets cytoplasmic components for their degradation and recycling in an autophagosome-dependent lysosomal manner. Under physiological conditions, this process maintains cellular homeostasis. However, autophagy can be stimulated upon different forms of cellular stress, ranging from nutrient starvation to exposure to drugs. Thus, this pathway can be seen as a central component of the integrated and adaptive stress response. Here, we report that even brief induction of autophagy is coupled in vitro to a persistent downregulation of the expression of MAP1LC3 isoforms, which are key components of the autophagy core machinery. In fact, DNA-methylation mediated by de novo DNA methyltransferase DNMT3A of MAP1LC3 loci upon autophagy stimulation leads to the observed long-term decrease of MAP1LC3 isoforms at transcriptional level. Finally, we report that the downregulation of MAP1LC3 expression can be observed in vivo in zebrafish larvae and mice exposed to a transient autophagy stimulus. This epigenetic memory of autophagy provides some understanding of the long-term effect of autophagy induction and offers a possible mechanism for its decline upon aging, pathological conditions, or in response to treatment interventions. Abbreviations: ACTB: actin beta; ATG: autophagy-related; 5-Aza: 5-aza-2’-deoxycytidine; BafA1: bafilomycin A(1); CBZ: carbamazepine; CDKN2A: cyclin dependent kinase inhibitor 2A; ChIP: chromatin immunoprecipitation; Clon.: clonidine; CpG: cytosine-guanine dinucleotide: DMSO: dimethyl sulfoxide; DNA: deoxyribonucleic acid; DNMT: DNA methyltransferase; DNMT1: DNA methyltransferase 1; DNMT3A: DNA methyltransferase alpha; DNMT3B: DNA methyltransferase beta; dpf: days post-fertilization; EBSS: Earle’s balanced salt solution; EM: Zebrafish embryo medium; GABARAP: GABA type A receptor associated protein; GABARAPL1: GABA type A receptor associated protein like 1; GABARAPL2: GABA type A receptor associated protein like 2; GAPDH: glyceraldehyde-3-phosphate dehydrogenase; GRO-Seq: Global Run-On sequencing; MAP1LC3/LC3: microtubule-associated protein 1 light chain 3; MAP1LC3A: microtubule-associated protein 1 light chain 3 alpha; MAP1LC3B: microtubule-associated protein 1 light chain 3 beta; MAP1LC3B2: microtubule-associated protein 1 light chain 3 beta 2; MEM: minimum essential medium; MEF: mouse embryonic fibroblasts; mRNA: messenger RNA; MTOR: mechanistic target of rapamycin kinase; PBS: phosphate-buffered saline; PIK3C3: phosphatidylinositol 3-kinase catalytic subunit type 3; RB1CC1/FIP200: RB1 inducible coiled-coil 1; RT-qPCR: quantitative reverse transcription polymerase chain reaction; SQSTM1/p62: sequestosome 1; Starv.: starvation; Treh.: trehalose; ULK1: unc-51 like autophagy activating kinase 1. Taylor & Francis 2020-09-14 /pmc/articles/PMC8143216/ /pubmed/32876528 http://dx.doi.org/10.1080/15548627.2020.1816664 Text en © 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
González-Rodríguez, Patricia
Cheray, Mathilde
Füllgrabe, Jens
Salli, Maria
Engskog-Vlachos, Pinelopi
Keane, Lily
Cunha, Virginia
Lupa, Agata
Li, Wenbo
Ma, Qi
Dreij, Kristian
Rosenfeld, Michael G.
Joseph, Bertrand
The DNA methyltransferase DNMT3A contributes to autophagy long-term memory
title The DNA methyltransferase DNMT3A contributes to autophagy long-term memory
title_full The DNA methyltransferase DNMT3A contributes to autophagy long-term memory
title_fullStr The DNA methyltransferase DNMT3A contributes to autophagy long-term memory
title_full_unstemmed The DNA methyltransferase DNMT3A contributes to autophagy long-term memory
title_short The DNA methyltransferase DNMT3A contributes to autophagy long-term memory
title_sort dna methyltransferase dnmt3a contributes to autophagy long-term memory
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8143216/
https://www.ncbi.nlm.nih.gov/pubmed/32876528
http://dx.doi.org/10.1080/15548627.2020.1816664
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