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Micro-RNAs, their target proteins, predispositions and the memory of filial imprinting

Visual imprinting is a learning process whereby young animals come to prefer a visual stimulus after exposure to it (training). The intermediate medial mesopallium (IMM) in the domestic chick forebrain is critical for visual imprinting and contributes to molecular regulation of memory formation. We...

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Autores principales: Margvelani, Giorgi, Meparishvili, Maia, Kiguradze, Tamar, McCabe, Brian J., Solomonia, Revaz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6262022/
https://www.ncbi.nlm.nih.gov/pubmed/30487553
http://dx.doi.org/10.1038/s41598-018-35097-w
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author Margvelani, Giorgi
Meparishvili, Maia
Kiguradze, Tamar
McCabe, Brian J.
Solomonia, Revaz
author_facet Margvelani, Giorgi
Meparishvili, Maia
Kiguradze, Tamar
McCabe, Brian J.
Solomonia, Revaz
author_sort Margvelani, Giorgi
collection PubMed
description Visual imprinting is a learning process whereby young animals come to prefer a visual stimulus after exposure to it (training). The intermediate medial mesopallium (IMM) in the domestic chick forebrain is critical for visual imprinting and contributes to molecular regulation of memory formation. We investigated the role of micro-RNAs (miRNAs) in such regulation. Twenty-four hours after training, miRNA spectra in the left IMM were compared between chicks with high preference scores (strong memory for imprinting stimulus), and chicks with low preference scores (weak memory for imprinting stimulus). Using criteria of significance and expression level, we chose gga-miR-130b-3p for further study and found that down-regulation correlated with learning strength. No effect was detected in posterior nidopallium, a region not involved in imprinting. We studied two targets of gga-miR-130b-3p, cytoplasmic polyadenylation element binding proteins 1 (CPEB-1) and 3 (CPEB-3), in two subcellular fractions (P2 membrane-mitochondrial and cytoplasmic) of IMM and posterior nidopallium. Only in the left IMM was a learning-related effect observed, in membrane CPEB-3. Variances from the regression with preference score and untrained chicks suggest that, in the IMM, gga-miR-130b-3p level reflects a predisposition, i.e. capacity to learn, whereas P2 membrane-mitochondrial CPEB-3 is up-regulated in a learning-specific way.
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spelling pubmed-62620222018-12-04 Micro-RNAs, their target proteins, predispositions and the memory of filial imprinting Margvelani, Giorgi Meparishvili, Maia Kiguradze, Tamar McCabe, Brian J. Solomonia, Revaz Sci Rep Article Visual imprinting is a learning process whereby young animals come to prefer a visual stimulus after exposure to it (training). The intermediate medial mesopallium (IMM) in the domestic chick forebrain is critical for visual imprinting and contributes to molecular regulation of memory formation. We investigated the role of micro-RNAs (miRNAs) in such regulation. Twenty-four hours after training, miRNA spectra in the left IMM were compared between chicks with high preference scores (strong memory for imprinting stimulus), and chicks with low preference scores (weak memory for imprinting stimulus). Using criteria of significance and expression level, we chose gga-miR-130b-3p for further study and found that down-regulation correlated with learning strength. No effect was detected in posterior nidopallium, a region not involved in imprinting. We studied two targets of gga-miR-130b-3p, cytoplasmic polyadenylation element binding proteins 1 (CPEB-1) and 3 (CPEB-3), in two subcellular fractions (P2 membrane-mitochondrial and cytoplasmic) of IMM and posterior nidopallium. Only in the left IMM was a learning-related effect observed, in membrane CPEB-3. Variances from the regression with preference score and untrained chicks suggest that, in the IMM, gga-miR-130b-3p level reflects a predisposition, i.e. capacity to learn, whereas P2 membrane-mitochondrial CPEB-3 is up-regulated in a learning-specific way. Nature Publishing Group UK 2018-11-28 /pmc/articles/PMC6262022/ /pubmed/30487553 http://dx.doi.org/10.1038/s41598-018-35097-w Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Margvelani, Giorgi
Meparishvili, Maia
Kiguradze, Tamar
McCabe, Brian J.
Solomonia, Revaz
Micro-RNAs, their target proteins, predispositions and the memory of filial imprinting
title Micro-RNAs, their target proteins, predispositions and the memory of filial imprinting
title_full Micro-RNAs, their target proteins, predispositions and the memory of filial imprinting
title_fullStr Micro-RNAs, their target proteins, predispositions and the memory of filial imprinting
title_full_unstemmed Micro-RNAs, their target proteins, predispositions and the memory of filial imprinting
title_short Micro-RNAs, their target proteins, predispositions and the memory of filial imprinting
title_sort micro-rnas, their target proteins, predispositions and the memory of filial imprinting
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6262022/
https://www.ncbi.nlm.nih.gov/pubmed/30487553
http://dx.doi.org/10.1038/s41598-018-35097-w
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