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Dnmts and Tet target memory-associated genes after appetitive olfactory training in honey bees
DNA methylation and demethylation are epigenetic mechanisms involved in memory formation. In honey bees DNA methyltransferase (Dnmt) function is necessary for long-term memory to be stimulus specific (i.e. to reduce generalization). So far, however, it remains elusive which genes are targeted and wh...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4632027/ https://www.ncbi.nlm.nih.gov/pubmed/26531238 http://dx.doi.org/10.1038/srep16223 |
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author | Biergans, Stephanie D. Giovanni Galizia, C. Reinhard, Judith Claudianos, Charles |
author_facet | Biergans, Stephanie D. Giovanni Galizia, C. Reinhard, Judith Claudianos, Charles |
author_sort | Biergans, Stephanie D. |
collection | PubMed |
description | DNA methylation and demethylation are epigenetic mechanisms involved in memory formation. In honey bees DNA methyltransferase (Dnmt) function is necessary for long-term memory to be stimulus specific (i.e. to reduce generalization). So far, however, it remains elusive which genes are targeted and what the time-course of DNA methylation is during memory formation. Here, we analyse how DNA methylation affects memory retention, gene expression, and differential methylation in stimulus-specific olfactory long-term memory formation. Out of 30 memory-associated genes investigated here, 9 were upregulated following Dnmt inhibition in trained bees. These included Dnmt3 suggesting a negative feedback loop for DNA methylation. Within these genes also the DNA methylation pattern changed during the first 24 hours after training. Interestingly, this was accompanied by sequential activation of the DNA methylation machinery (i.e. Dnmts and Tet). In sum, memory formation involves a temporally complex epigenetic regulation of memory-associated genes that facilitates stimulus specific long-term memory in the honey bee. |
format | Online Article Text |
id | pubmed-4632027 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46320272015-12-07 Dnmts and Tet target memory-associated genes after appetitive olfactory training in honey bees Biergans, Stephanie D. Giovanni Galizia, C. Reinhard, Judith Claudianos, Charles Sci Rep Article DNA methylation and demethylation are epigenetic mechanisms involved in memory formation. In honey bees DNA methyltransferase (Dnmt) function is necessary for long-term memory to be stimulus specific (i.e. to reduce generalization). So far, however, it remains elusive which genes are targeted and what the time-course of DNA methylation is during memory formation. Here, we analyse how DNA methylation affects memory retention, gene expression, and differential methylation in stimulus-specific olfactory long-term memory formation. Out of 30 memory-associated genes investigated here, 9 were upregulated following Dnmt inhibition in trained bees. These included Dnmt3 suggesting a negative feedback loop for DNA methylation. Within these genes also the DNA methylation pattern changed during the first 24 hours after training. Interestingly, this was accompanied by sequential activation of the DNA methylation machinery (i.e. Dnmts and Tet). In sum, memory formation involves a temporally complex epigenetic regulation of memory-associated genes that facilitates stimulus specific long-term memory in the honey bee. Nature Publishing Group 2015-11-04 /pmc/articles/PMC4632027/ /pubmed/26531238 http://dx.doi.org/10.1038/srep16223 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Biergans, Stephanie D. Giovanni Galizia, C. Reinhard, Judith Claudianos, Charles Dnmts and Tet target memory-associated genes after appetitive olfactory training in honey bees |
title | Dnmts and Tet target memory-associated genes after appetitive olfactory training in honey bees |
title_full | Dnmts and Tet target memory-associated genes after appetitive olfactory training in honey bees |
title_fullStr | Dnmts and Tet target memory-associated genes after appetitive olfactory training in honey bees |
title_full_unstemmed | Dnmts and Tet target memory-associated genes after appetitive olfactory training in honey bees |
title_short | Dnmts and Tet target memory-associated genes after appetitive olfactory training in honey bees |
title_sort | dnmts and tet target memory-associated genes after appetitive olfactory training in honey bees |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4632027/ https://www.ncbi.nlm.nih.gov/pubmed/26531238 http://dx.doi.org/10.1038/srep16223 |
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