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Fluid consumption and taste novelty determines transcription temporal dynamics in the gustatory cortex
BACKGROUND: Novel taste memories, critical for animal survival, are consolidated to form long term memories which are dependent on translation regulation in the gustatory cortex (GC) hours following acquisition. However, the role of transcription regulation in the process is unknown. RESULTS: Here,...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4746785/ https://www.ncbi.nlm.nih.gov/pubmed/26856319 http://dx.doi.org/10.1186/s13041-016-0188-4 |
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author | Inberg, Sharon Jacob, Eyal Elkobi, Alina Edry, Efrat Rappaport, Akiva Simpson, T. Ian Armstrong, J. Douglas Shomron, Noam Pasmanik-Chor, Metsada Rosenblum, Kobi |
author_facet | Inberg, Sharon Jacob, Eyal Elkobi, Alina Edry, Efrat Rappaport, Akiva Simpson, T. Ian Armstrong, J. Douglas Shomron, Noam Pasmanik-Chor, Metsada Rosenblum, Kobi |
author_sort | Inberg, Sharon |
collection | PubMed |
description | BACKGROUND: Novel taste memories, critical for animal survival, are consolidated to form long term memories which are dependent on translation regulation in the gustatory cortex (GC) hours following acquisition. However, the role of transcription regulation in the process is unknown. RESULTS: Here, we report that transcription in the GC is necessary for taste learning in rats, and that drinking and its consequences, as well as the novel taste experience, affect transcription in the GC during taste memory consolidation. We show differential effects of learning on temporal dynamics in set of genes in the GC, including Arc/Arg3.1, known to regulate the homeostasis of excitatory synapses. CONCLUSIONS: We demonstrate that in taste learning, transcription programs were activated following the physiological responses (i.e., fluid consumption following a water restriction regime, reward, arousal of the animal, etc.) and the specific information about a given taste (i.e., taste novelty). Moreover, the cortical differential prolonged kinetics of mRNA following novel versus familiar taste learning may represent additional novelty related molecular response, where not only the total amount, but also the temporal dynamics of transcription is modulated by sensory experience of novel information. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13041-016-0188-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4746785 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-47467852016-02-10 Fluid consumption and taste novelty determines transcription temporal dynamics in the gustatory cortex Inberg, Sharon Jacob, Eyal Elkobi, Alina Edry, Efrat Rappaport, Akiva Simpson, T. Ian Armstrong, J. Douglas Shomron, Noam Pasmanik-Chor, Metsada Rosenblum, Kobi Mol Brain Research BACKGROUND: Novel taste memories, critical for animal survival, are consolidated to form long term memories which are dependent on translation regulation in the gustatory cortex (GC) hours following acquisition. However, the role of transcription regulation in the process is unknown. RESULTS: Here, we report that transcription in the GC is necessary for taste learning in rats, and that drinking and its consequences, as well as the novel taste experience, affect transcription in the GC during taste memory consolidation. We show differential effects of learning on temporal dynamics in set of genes in the GC, including Arc/Arg3.1, known to regulate the homeostasis of excitatory synapses. CONCLUSIONS: We demonstrate that in taste learning, transcription programs were activated following the physiological responses (i.e., fluid consumption following a water restriction regime, reward, arousal of the animal, etc.) and the specific information about a given taste (i.e., taste novelty). Moreover, the cortical differential prolonged kinetics of mRNA following novel versus familiar taste learning may represent additional novelty related molecular response, where not only the total amount, but also the temporal dynamics of transcription is modulated by sensory experience of novel information. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13041-016-0188-4) contains supplementary material, which is available to authorized users. BioMed Central 2016-02-09 /pmc/articles/PMC4746785/ /pubmed/26856319 http://dx.doi.org/10.1186/s13041-016-0188-4 Text en © Inberg et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Inberg, Sharon Jacob, Eyal Elkobi, Alina Edry, Efrat Rappaport, Akiva Simpson, T. Ian Armstrong, J. Douglas Shomron, Noam Pasmanik-Chor, Metsada Rosenblum, Kobi Fluid consumption and taste novelty determines transcription temporal dynamics in the gustatory cortex |
title | Fluid consumption and taste novelty determines transcription temporal dynamics in the gustatory cortex |
title_full | Fluid consumption and taste novelty determines transcription temporal dynamics in the gustatory cortex |
title_fullStr | Fluid consumption and taste novelty determines transcription temporal dynamics in the gustatory cortex |
title_full_unstemmed | Fluid consumption and taste novelty determines transcription temporal dynamics in the gustatory cortex |
title_short | Fluid consumption and taste novelty determines transcription temporal dynamics in the gustatory cortex |
title_sort | fluid consumption and taste novelty determines transcription temporal dynamics in the gustatory cortex |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4746785/ https://www.ncbi.nlm.nih.gov/pubmed/26856319 http://dx.doi.org/10.1186/s13041-016-0188-4 |
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