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Using the canary genome to decipher the evolution of hormone-sensitive gene regulation in seasonal singing birds

BACKGROUND: While the song of all songbirds is controlled by the same neural circuit, the hormone dependence of singing behavior varies greatly between species. For this reason, songbirds are ideal organisms to study ultimate and proximate mechanisms of hormone-dependent behavior and neuronal plasti...

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Autores principales: Frankl-Vilches, Carolina, Kuhl, Heiner, Werber, Martin, Klages, Sven, Kerick, Martin, Bakker, Antje, de Oliveira, Edivaldo HC, Reusch, Christina, Capuano, Floriana, Vowinckel, Jakob, Leitner, Stefan, Ralser, Markus, Timmermann, Bernd, Gahr, Manfred
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4373106/
https://www.ncbi.nlm.nih.gov/pubmed/25631560
http://dx.doi.org/10.1186/s13059-014-0578-9
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author Frankl-Vilches, Carolina
Kuhl, Heiner
Werber, Martin
Klages, Sven
Kerick, Martin
Bakker, Antje
de Oliveira, Edivaldo HC
Reusch, Christina
Capuano, Floriana
Vowinckel, Jakob
Leitner, Stefan
Ralser, Markus
Timmermann, Bernd
Gahr, Manfred
author_facet Frankl-Vilches, Carolina
Kuhl, Heiner
Werber, Martin
Klages, Sven
Kerick, Martin
Bakker, Antje
de Oliveira, Edivaldo HC
Reusch, Christina
Capuano, Floriana
Vowinckel, Jakob
Leitner, Stefan
Ralser, Markus
Timmermann, Bernd
Gahr, Manfred
author_sort Frankl-Vilches, Carolina
collection PubMed
description BACKGROUND: While the song of all songbirds is controlled by the same neural circuit, the hormone dependence of singing behavior varies greatly between species. For this reason, songbirds are ideal organisms to study ultimate and proximate mechanisms of hormone-dependent behavior and neuronal plasticity. RESULTS: We present the high quality assembly and annotation of a female 1.2-Gbp canary genome. Whole genome alignments between the canary and 13 genomes throughout the bird taxa show a much-conserved synteny, whereas at the single-base resolution there are considerable species differences. These differences impact small sequence motifs like transcription factor binding sites such as estrogen response elements and androgen response elements. To relate these species-specific response elements to the hormone-sensitivity of the canary singing behavior, we identify seasonal testosterone-sensitive transcriptomes of major song-related brain regions, HVC and RA, and find the seasonal gene networks related to neuronal differentiation only in the HVC. Testosterone-sensitive up-regulated gene networks of HVC of singing males concerned neuronal differentiation. Among the testosterone-regulated genes of canary HVC, 20% lack estrogen response elements and 4 to 8% lack androgen response elements in orthologous promoters in the zebra finch. CONCLUSIONS: The canary genome sequence and complementary expression analysis reveal intra-regional evolutionary changes in a multi-regional neural circuit controlling seasonal singing behavior and identify gene evolution related to the hormone-sensitivity of this seasonal singing behavior. Such genes that are testosterone- and estrogen-sensitive specifically in the canary and that are involved in rewiring of neurons might be crucial for seasonal re-differentiation of HVC underlying seasonal song patterning. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-014-0578-9) contains supplementary material, which is available to authorized users.
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spelling pubmed-43731062015-03-26 Using the canary genome to decipher the evolution of hormone-sensitive gene regulation in seasonal singing birds Frankl-Vilches, Carolina Kuhl, Heiner Werber, Martin Klages, Sven Kerick, Martin Bakker, Antje de Oliveira, Edivaldo HC Reusch, Christina Capuano, Floriana Vowinckel, Jakob Leitner, Stefan Ralser, Markus Timmermann, Bernd Gahr, Manfred Genome Biol Research BACKGROUND: While the song of all songbirds is controlled by the same neural circuit, the hormone dependence of singing behavior varies greatly between species. For this reason, songbirds are ideal organisms to study ultimate and proximate mechanisms of hormone-dependent behavior and neuronal plasticity. RESULTS: We present the high quality assembly and annotation of a female 1.2-Gbp canary genome. Whole genome alignments between the canary and 13 genomes throughout the bird taxa show a much-conserved synteny, whereas at the single-base resolution there are considerable species differences. These differences impact small sequence motifs like transcription factor binding sites such as estrogen response elements and androgen response elements. To relate these species-specific response elements to the hormone-sensitivity of the canary singing behavior, we identify seasonal testosterone-sensitive transcriptomes of major song-related brain regions, HVC and RA, and find the seasonal gene networks related to neuronal differentiation only in the HVC. Testosterone-sensitive up-regulated gene networks of HVC of singing males concerned neuronal differentiation. Among the testosterone-regulated genes of canary HVC, 20% lack estrogen response elements and 4 to 8% lack androgen response elements in orthologous promoters in the zebra finch. CONCLUSIONS: The canary genome sequence and complementary expression analysis reveal intra-regional evolutionary changes in a multi-regional neural circuit controlling seasonal singing behavior and identify gene evolution related to the hormone-sensitivity of this seasonal singing behavior. Such genes that are testosterone- and estrogen-sensitive specifically in the canary and that are involved in rewiring of neurons might be crucial for seasonal re-differentiation of HVC underlying seasonal song patterning. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-014-0578-9) contains supplementary material, which is available to authorized users. BioMed Central 2015-01-29 2015 /pmc/articles/PMC4373106/ /pubmed/25631560 http://dx.doi.org/10.1186/s13059-014-0578-9 Text en © Frankl-Vilches et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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
Frankl-Vilches, Carolina
Kuhl, Heiner
Werber, Martin
Klages, Sven
Kerick, Martin
Bakker, Antje
de Oliveira, Edivaldo HC
Reusch, Christina
Capuano, Floriana
Vowinckel, Jakob
Leitner, Stefan
Ralser, Markus
Timmermann, Bernd
Gahr, Manfred
Using the canary genome to decipher the evolution of hormone-sensitive gene regulation in seasonal singing birds
title Using the canary genome to decipher the evolution of hormone-sensitive gene regulation in seasonal singing birds
title_full Using the canary genome to decipher the evolution of hormone-sensitive gene regulation in seasonal singing birds
title_fullStr Using the canary genome to decipher the evolution of hormone-sensitive gene regulation in seasonal singing birds
title_full_unstemmed Using the canary genome to decipher the evolution of hormone-sensitive gene regulation in seasonal singing birds
title_short Using the canary genome to decipher the evolution of hormone-sensitive gene regulation in seasonal singing birds
title_sort using the canary genome to decipher the evolution of hormone-sensitive gene regulation in seasonal singing birds
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4373106/
https://www.ncbi.nlm.nih.gov/pubmed/25631560
http://dx.doi.org/10.1186/s13059-014-0578-9
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