Cargando…
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...
Autores principales: | , , , , , , , , , , , , , |
---|---|
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 |
_version_ | 1782363292419751936 |
---|---|
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. |
format | Online Article Text |
id | pubmed-4373106 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT franklvilchescarolina usingthecanarygenometodeciphertheevolutionofhormonesensitivegeneregulationinseasonalsingingbirds AT kuhlheiner usingthecanarygenometodeciphertheevolutionofhormonesensitivegeneregulationinseasonalsingingbirds AT werbermartin usingthecanarygenometodeciphertheevolutionofhormonesensitivegeneregulationinseasonalsingingbirds AT klagessven usingthecanarygenometodeciphertheevolutionofhormonesensitivegeneregulationinseasonalsingingbirds AT kerickmartin usingthecanarygenometodeciphertheevolutionofhormonesensitivegeneregulationinseasonalsingingbirds AT bakkerantje usingthecanarygenometodeciphertheevolutionofhormonesensitivegeneregulationinseasonalsingingbirds AT deoliveiraedivaldohc usingthecanarygenometodeciphertheevolutionofhormonesensitivegeneregulationinseasonalsingingbirds AT reuschchristina usingthecanarygenometodeciphertheevolutionofhormonesensitivegeneregulationinseasonalsingingbirds AT capuanofloriana usingthecanarygenometodeciphertheevolutionofhormonesensitivegeneregulationinseasonalsingingbirds AT vowinckeljakob usingthecanarygenometodeciphertheevolutionofhormonesensitivegeneregulationinseasonalsingingbirds AT leitnerstefan usingthecanarygenometodeciphertheevolutionofhormonesensitivegeneregulationinseasonalsingingbirds AT ralsermarkus usingthecanarygenometodeciphertheevolutionofhormonesensitivegeneregulationinseasonalsingingbirds AT timmermannbernd usingthecanarygenometodeciphertheevolutionofhormonesensitivegeneregulationinseasonalsingingbirds AT gahrmanfred usingthecanarygenometodeciphertheevolutionofhormonesensitivegeneregulationinseasonalsingingbirds |