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Seasonal Changes in Patterns of Gene Expression in Avian Song Control Brain Regions

Photoperiod and hormonal cues drive dramatic seasonal changes in structure and function of the avian song control system. Little is known, however, about the patterns of gene expression associated with seasonal changes. Here we address this issue by altering the hormonal and photoperiodic conditions...

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Autores principales: Thompson, Christopher K., Meitzen, John, Replogle, Kirstin, Drnevich, Jenny, Lent, Karin L., Wissman, Anne Marie, Farin, Federico M., Bammler, Theo K., Beyer, Richard P., Clayton, David F., Perkel, David J., Brenowitz, Eliot A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3329558/
https://www.ncbi.nlm.nih.gov/pubmed/22529977
http://dx.doi.org/10.1371/journal.pone.0035119
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author Thompson, Christopher K.
Meitzen, John
Replogle, Kirstin
Drnevich, Jenny
Lent, Karin L.
Wissman, Anne Marie
Farin, Federico M.
Bammler, Theo K.
Beyer, Richard P.
Clayton, David F.
Perkel, David J.
Brenowitz, Eliot A.
author_facet Thompson, Christopher K.
Meitzen, John
Replogle, Kirstin
Drnevich, Jenny
Lent, Karin L.
Wissman, Anne Marie
Farin, Federico M.
Bammler, Theo K.
Beyer, Richard P.
Clayton, David F.
Perkel, David J.
Brenowitz, Eliot A.
author_sort Thompson, Christopher K.
collection PubMed
description Photoperiod and hormonal cues drive dramatic seasonal changes in structure and function of the avian song control system. Little is known, however, about the patterns of gene expression associated with seasonal changes. Here we address this issue by altering the hormonal and photoperiodic conditions in seasonally-breeding Gambel's white-crowned sparrows and extracting RNA from the telencephalic song control nuclei HVC and RA across multiple time points that capture different stages of growth and regression. We chose HVC and RA because while both nuclei change in volume across seasons, the cellular mechanisms underlying these changes differ. We thus hypothesized that different genes would be expressed between HVC and RA. We tested this by using the extracted RNA to perform a cDNA microarray hybridization developed by the SoNG initiative. We then validated these results using qRT-PCR. We found that 363 genes varied by more than 1.5 fold (>log(2) 0.585) in expression in HVC and/or RA. Supporting our hypothesis, only 59 of these 363 genes were found to vary in both nuclei, while 132 gene expression changes were HVC specific and 172 were RA specific. We then assigned many of these genes to functional categories relevant to the different mechanisms underlying seasonal change in HVC and RA, including neurogenesis, apoptosis, cell growth, dendrite arborization and axonal growth, angiogenesis, endocrinology, growth factors, and electrophysiology. This revealed categorical differences in the kinds of genes regulated in HVC and RA. These results show that different molecular programs underlie seasonal changes in HVC and RA, and that gene expression is time specific across different reproductive conditions. Our results provide insights into the complex molecular pathways that underlie adult neural plasticity.
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spelling pubmed-33295582012-04-23 Seasonal Changes in Patterns of Gene Expression in Avian Song Control Brain Regions Thompson, Christopher K. Meitzen, John Replogle, Kirstin Drnevich, Jenny Lent, Karin L. Wissman, Anne Marie Farin, Federico M. Bammler, Theo K. Beyer, Richard P. Clayton, David F. Perkel, David J. Brenowitz, Eliot A. PLoS One Research Article Photoperiod and hormonal cues drive dramatic seasonal changes in structure and function of the avian song control system. Little is known, however, about the patterns of gene expression associated with seasonal changes. Here we address this issue by altering the hormonal and photoperiodic conditions in seasonally-breeding Gambel's white-crowned sparrows and extracting RNA from the telencephalic song control nuclei HVC and RA across multiple time points that capture different stages of growth and regression. We chose HVC and RA because while both nuclei change in volume across seasons, the cellular mechanisms underlying these changes differ. We thus hypothesized that different genes would be expressed between HVC and RA. We tested this by using the extracted RNA to perform a cDNA microarray hybridization developed by the SoNG initiative. We then validated these results using qRT-PCR. We found that 363 genes varied by more than 1.5 fold (>log(2) 0.585) in expression in HVC and/or RA. Supporting our hypothesis, only 59 of these 363 genes were found to vary in both nuclei, while 132 gene expression changes were HVC specific and 172 were RA specific. We then assigned many of these genes to functional categories relevant to the different mechanisms underlying seasonal change in HVC and RA, including neurogenesis, apoptosis, cell growth, dendrite arborization and axonal growth, angiogenesis, endocrinology, growth factors, and electrophysiology. This revealed categorical differences in the kinds of genes regulated in HVC and RA. These results show that different molecular programs underlie seasonal changes in HVC and RA, and that gene expression is time specific across different reproductive conditions. Our results provide insights into the complex molecular pathways that underlie adult neural plasticity. Public Library of Science 2012-04-18 /pmc/articles/PMC3329558/ /pubmed/22529977 http://dx.doi.org/10.1371/journal.pone.0035119 Text en Thompson et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Thompson, Christopher K.
Meitzen, John
Replogle, Kirstin
Drnevich, Jenny
Lent, Karin L.
Wissman, Anne Marie
Farin, Federico M.
Bammler, Theo K.
Beyer, Richard P.
Clayton, David F.
Perkel, David J.
Brenowitz, Eliot A.
Seasonal Changes in Patterns of Gene Expression in Avian Song Control Brain Regions
title Seasonal Changes in Patterns of Gene Expression in Avian Song Control Brain Regions
title_full Seasonal Changes in Patterns of Gene Expression in Avian Song Control Brain Regions
title_fullStr Seasonal Changes in Patterns of Gene Expression in Avian Song Control Brain Regions
title_full_unstemmed Seasonal Changes in Patterns of Gene Expression in Avian Song Control Brain Regions
title_short Seasonal Changes in Patterns of Gene Expression in Avian Song Control Brain Regions
title_sort seasonal changes in patterns of gene expression in avian song control brain regions
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3329558/
https://www.ncbi.nlm.nih.gov/pubmed/22529977
http://dx.doi.org/10.1371/journal.pone.0035119
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