Epigenetic regulation of learning and memory by Drosophila EHMT/G9a.

The epigenetic modification of chromatin structure and its effect on complex neuronal processes like learning and memory is an emerging field in neuroscience. However, little is known about the "writers" of the neuronal epigenome and how they lay down the basis for proper cognition. Here,...

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Autores principales: Jamie M Kramer, Korinna Kochinke, Merel A W Oortveld, Hendrik Marks, Daniela Kramer, Eiko K de Jong, Zoltan Asztalos, J Timothy Westwood, Hendrik G Stunnenberg, Marla B Sokolowski, Krystyna Keleman, Huiqing Zhou, Hans van Bokhoven, Annette Schenck
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Publicado: Public Library of Science (PLoS) 2011
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Acceso en línea:https://doaj.org/article/44311756665c4430a37ca1a49ede9c96
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spelling oai:doaj.org-article:44311756665c4430a37ca1a49ede9c962021-11-18T05:36:23ZEpigenetic regulation of learning and memory by Drosophila EHMT/G9a.1544-91731545-788510.1371/journal.pbio.1000569https://doaj.org/article/44311756665c4430a37ca1a49ede9c962011-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21245904/pdf/?tool=EBIhttps://doaj.org/toc/1544-9173https://doaj.org/toc/1545-7885The epigenetic modification of chromatin structure and its effect on complex neuronal processes like learning and memory is an emerging field in neuroscience. However, little is known about the "writers" of the neuronal epigenome and how they lay down the basis for proper cognition. Here, we have dissected the neuronal function of the Drosophila euchromatin histone methyltransferase (EHMT), a member of a conserved protein family that methylates histone 3 at lysine 9 (H3K9). EHMT is widely expressed in the nervous system and other tissues, yet EHMT mutant flies are viable. Neurodevelopmental and behavioral analyses identified EHMT as a regulator of peripheral dendrite development, larval locomotor behavior, non-associative learning, and courtship memory. The requirement for EHMT in memory was mapped to 7B-Gal4 positive cells, which are, in adult brains, predominantly mushroom body neurons. Moreover, memory was restored by EHMT re-expression during adulthood, indicating that cognitive defects are reversible in EHMT mutants. To uncover the underlying molecular mechanisms, we generated genome-wide H3K9 dimethylation profiles by ChIP-seq. Loss of H3K9 dimethylation in EHMT mutants occurs at 5% of the euchromatic genome and is enriched at the 5' and 3' ends of distinct classes of genes that control neuronal and behavioral processes that are corrupted in EHMT mutants. Our study identifies Drosophila EHMT as a key regulator of cognition that orchestrates an epigenetic program featuring classic learning and memory genes. Our findings are relevant to the pathophysiological mechanisms underlying Kleefstra Syndrome, a severe form of intellectual disability caused by mutations in human EHMT1, and have potential therapeutic implications. Our work thus provides novel insights into the epigenetic control of cognition in health and disease.Jamie M KramerKorinna KochinkeMerel A W OortveldHendrik MarksDaniela KramerEiko K de JongZoltan AsztalosJ Timothy WestwoodHendrik G StunnenbergMarla B SokolowskiKrystyna KelemanHuiqing ZhouHans van BokhovenAnnette SchenckPublic Library of Science (PLoS)articleBiology (General)QH301-705.5ENPLoS Biology, Vol 9, Iss 1, p e1000569 (2011)
institution DOAJ
collection DOAJ
language EN
topic Biology (General)
QH301-705.5
spellingShingle Biology (General)
QH301-705.5
Jamie M Kramer
Korinna Kochinke
Merel A W Oortveld
Hendrik Marks
Daniela Kramer
Eiko K de Jong
Zoltan Asztalos
J Timothy Westwood
Hendrik G Stunnenberg
Marla B Sokolowski
Krystyna Keleman
Huiqing Zhou
Hans van Bokhoven
Annette Schenck
Epigenetic regulation of learning and memory by Drosophila EHMT/G9a.
description The epigenetic modification of chromatin structure and its effect on complex neuronal processes like learning and memory is an emerging field in neuroscience. However, little is known about the "writers" of the neuronal epigenome and how they lay down the basis for proper cognition. Here, we have dissected the neuronal function of the Drosophila euchromatin histone methyltransferase (EHMT), a member of a conserved protein family that methylates histone 3 at lysine 9 (H3K9). EHMT is widely expressed in the nervous system and other tissues, yet EHMT mutant flies are viable. Neurodevelopmental and behavioral analyses identified EHMT as a regulator of peripheral dendrite development, larval locomotor behavior, non-associative learning, and courtship memory. The requirement for EHMT in memory was mapped to 7B-Gal4 positive cells, which are, in adult brains, predominantly mushroom body neurons. Moreover, memory was restored by EHMT re-expression during adulthood, indicating that cognitive defects are reversible in EHMT mutants. To uncover the underlying molecular mechanisms, we generated genome-wide H3K9 dimethylation profiles by ChIP-seq. Loss of H3K9 dimethylation in EHMT mutants occurs at 5% of the euchromatic genome and is enriched at the 5' and 3' ends of distinct classes of genes that control neuronal and behavioral processes that are corrupted in EHMT mutants. Our study identifies Drosophila EHMT as a key regulator of cognition that orchestrates an epigenetic program featuring classic learning and memory genes. Our findings are relevant to the pathophysiological mechanisms underlying Kleefstra Syndrome, a severe form of intellectual disability caused by mutations in human EHMT1, and have potential therapeutic implications. Our work thus provides novel insights into the epigenetic control of cognition in health and disease.
format article
author Jamie M Kramer
Korinna Kochinke
Merel A W Oortveld
Hendrik Marks
Daniela Kramer
Eiko K de Jong
Zoltan Asztalos
J Timothy Westwood
Hendrik G Stunnenberg
Marla B Sokolowski
Krystyna Keleman
Huiqing Zhou
Hans van Bokhoven
Annette Schenck
author_facet Jamie M Kramer
Korinna Kochinke
Merel A W Oortveld
Hendrik Marks
Daniela Kramer
Eiko K de Jong
Zoltan Asztalos
J Timothy Westwood
Hendrik G Stunnenberg
Marla B Sokolowski
Krystyna Keleman
Huiqing Zhou
Hans van Bokhoven
Annette Schenck
author_sort Jamie M Kramer
title Epigenetic regulation of learning and memory by Drosophila EHMT/G9a.
title_short Epigenetic regulation of learning and memory by Drosophila EHMT/G9a.
title_full Epigenetic regulation of learning and memory by Drosophila EHMT/G9a.
title_fullStr Epigenetic regulation of learning and memory by Drosophila EHMT/G9a.
title_full_unstemmed Epigenetic regulation of learning and memory by Drosophila EHMT/G9a.
title_sort epigenetic regulation of learning and memory by drosophila ehmt/g9a.
publisher Public Library of Science (PLoS)
publishDate 2011
url https://doaj.org/article/44311756665c4430a37ca1a49ede9c96
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