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Olfactory discrimination training up-regulates and reorganizes expression of microRNAs in adult mouse hippocampus

Adult male mice (strain C57Bl/6J) were trained to execute nose-poke responses for water reinforcement; then they were randomly assigned to either of two groups: olfactory discrimination training (exposed to two odours with reward contingent upon correctly responding to one odour) or pseudo-training...

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Autores principales: Smalheiser, Neil R, Lugli, Giovanni, Lenon, Angela L, Davis, John M, Torvik, Vetle I, Larson, John
Formato: Texto
Lenguaje:English
Publicado: American Society for Neurochemistry 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2832745/
https://www.ncbi.nlm.nih.gov/pubmed/20309390
http://dx.doi.org/10.1042/AN20090055
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author Smalheiser, Neil R
Lugli, Giovanni
Lenon, Angela L
Davis, John M
Torvik, Vetle I
Larson, John
author_facet Smalheiser, Neil R
Lugli, Giovanni
Lenon, Angela L
Davis, John M
Torvik, Vetle I
Larson, John
author_sort Smalheiser, Neil R
collection PubMed
description Adult male mice (strain C57Bl/6J) were trained to execute nose-poke responses for water reinforcement; then they were randomly assigned to either of two groups: olfactory discrimination training (exposed to two odours with reward contingent upon correctly responding to one odour) or pseudo-training (exposed to two odours with reward not contingent upon response). These were run in yoked fashion and killed when the discrimination-trained mouse reached a learning criterion of 70% correct responses in 20 trials, occurring after three sessions (a total of ∼40 min of training). The hippocampus was dissected bilaterally from each mouse (N = 7 in each group) and profiling of 585 miRNAs (microRNAs) was carried out using multiplex RT–PCR (reverse transcription–PCR) plates. A significant global up-regulation of miRNA expression was observed in the discrimination training versus pseudo-training comparison; when tested individually, 29 miRNAs achieved significance at P = 0.05. miR-10a showed a 2.7-fold increase with training, and is predicted to target several learning-related mRNAs including BDNF (brain-derived neurotrophic factor), CAMK2b (calcium/calmodulin-dependent protein kinase IIβ), CREB1 (cAMP-response-element-binding protein 1) and ELAVL2 [ELAV (embryonic lethal, abnormal vision, Drosophila)-like; Hu B]. Analysis of miRNA pairwise correlations revealed the existence of several miRNA co-expression modules that were specific to the training group. These in vivo results indicate that significant, dynamic and co-ordinated changes in miRNA expression accompany early stages of learning.
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spelling pubmed-28327452010-03-22 Olfactory discrimination training up-regulates and reorganizes expression of microRNAs in adult mouse hippocampus Smalheiser, Neil R Lugli, Giovanni Lenon, Angela L Davis, John M Torvik, Vetle I Larson, John ASN Neuro Research article Adult male mice (strain C57Bl/6J) were trained to execute nose-poke responses for water reinforcement; then they were randomly assigned to either of two groups: olfactory discrimination training (exposed to two odours with reward contingent upon correctly responding to one odour) or pseudo-training (exposed to two odours with reward not contingent upon response). These were run in yoked fashion and killed when the discrimination-trained mouse reached a learning criterion of 70% correct responses in 20 trials, occurring after three sessions (a total of ∼40 min of training). The hippocampus was dissected bilaterally from each mouse (N = 7 in each group) and profiling of 585 miRNAs (microRNAs) was carried out using multiplex RT–PCR (reverse transcription–PCR) plates. A significant global up-regulation of miRNA expression was observed in the discrimination training versus pseudo-training comparison; when tested individually, 29 miRNAs achieved significance at P = 0.05. miR-10a showed a 2.7-fold increase with training, and is predicted to target several learning-related mRNAs including BDNF (brain-derived neurotrophic factor), CAMK2b (calcium/calmodulin-dependent protein kinase IIβ), CREB1 (cAMP-response-element-binding protein 1) and ELAVL2 [ELAV (embryonic lethal, abnormal vision, Drosophila)-like; Hu B]. Analysis of miRNA pairwise correlations revealed the existence of several miRNA co-expression modules that were specific to the training group. These in vivo results indicate that significant, dynamic and co-ordinated changes in miRNA expression accompany early stages of learning. American Society for Neurochemistry 2010-02-26 /pmc/articles/PMC2832745/ /pubmed/20309390 http://dx.doi.org/10.1042/AN20090055 Text en © 2010 The Author(s). http://creativecommons.org/licenses/by-nc/2.5/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial Licence (http://creativecommons.org/licenses/by-nc/2.5/) which permits unrestricted non-commercial use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research article
Smalheiser, Neil R
Lugli, Giovanni
Lenon, Angela L
Davis, John M
Torvik, Vetle I
Larson, John
Olfactory discrimination training up-regulates and reorganizes expression of microRNAs in adult mouse hippocampus
title Olfactory discrimination training up-regulates and reorganizes expression of microRNAs in adult mouse hippocampus
title_full Olfactory discrimination training up-regulates and reorganizes expression of microRNAs in adult mouse hippocampus
title_fullStr Olfactory discrimination training up-regulates and reorganizes expression of microRNAs in adult mouse hippocampus
title_full_unstemmed Olfactory discrimination training up-regulates and reorganizes expression of microRNAs in adult mouse hippocampus
title_short Olfactory discrimination training up-regulates and reorganizes expression of microRNAs in adult mouse hippocampus
title_sort olfactory discrimination training up-regulates and reorganizes expression of micrornas in adult mouse hippocampus
topic Research article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2832745/
https://www.ncbi.nlm.nih.gov/pubmed/20309390
http://dx.doi.org/10.1042/AN20090055
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