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Convergent Differential Regulation of Parvalbumin in the Brains of Vocal Learners

Spoken language and learned song are complex communication behaviors found in only a few species, including humans and three groups of distantly related birds – songbirds, parrots, and hummingbirds. Despite their large phylogenetic distances, these vocal learners show convergent behaviors and associ...

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Autores principales: Hara, Erina, Rivas, Miriam V., Ward, James M., Okanoya, Kazuo, Jarvis, Erich D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253077/
https://www.ncbi.nlm.nih.gov/pubmed/22238614
http://dx.doi.org/10.1371/journal.pone.0029457
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author Hara, Erina
Rivas, Miriam V.
Ward, James M.
Okanoya, Kazuo
Jarvis, Erich D.
author_facet Hara, Erina
Rivas, Miriam V.
Ward, James M.
Okanoya, Kazuo
Jarvis, Erich D.
author_sort Hara, Erina
collection PubMed
description Spoken language and learned song are complex communication behaviors found in only a few species, including humans and three groups of distantly related birds – songbirds, parrots, and hummingbirds. Despite their large phylogenetic distances, these vocal learners show convergent behaviors and associated brain pathways for vocal communication. However, it is not clear whether this behavioral and anatomical convergence is associated with molecular convergence. Here we used oligo microarrays to screen for genes differentially regulated in brain nuclei necessary for producing learned vocalizations relative to adjacent brain areas that control other behaviors in avian vocal learners versus vocal non-learners. A top candidate gene in our screen was a calcium-binding protein, parvalbumin (PV). In situ hybridization verification revealed that PV was expressed significantly higher throughout the song motor pathway, including brainstem vocal motor neurons relative to the surrounding brain regions of all distantly related avian vocal learners. This differential expression was specific to PV and vocal learners, as it was not found in avian vocal non-learners nor for control genes in learners and non-learners. Similar to the vocal learning birds, higher PV up-regulation was found in the brainstem tongue motor neurons used for speech production in humans relative to a non-human primate, macaques. These results suggest repeated convergent evolution of differential PV up-regulation in the brains of vocal learners separated by more than 65–300 million years from a common ancestor and that the specialized behaviors of learned song and speech may require extra calcium buffering and signaling.
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spelling pubmed-32530772012-01-11 Convergent Differential Regulation of Parvalbumin in the Brains of Vocal Learners Hara, Erina Rivas, Miriam V. Ward, James M. Okanoya, Kazuo Jarvis, Erich D. PLoS One Research Article Spoken language and learned song are complex communication behaviors found in only a few species, including humans and three groups of distantly related birds – songbirds, parrots, and hummingbirds. Despite their large phylogenetic distances, these vocal learners show convergent behaviors and associated brain pathways for vocal communication. However, it is not clear whether this behavioral and anatomical convergence is associated with molecular convergence. Here we used oligo microarrays to screen for genes differentially regulated in brain nuclei necessary for producing learned vocalizations relative to adjacent brain areas that control other behaviors in avian vocal learners versus vocal non-learners. A top candidate gene in our screen was a calcium-binding protein, parvalbumin (PV). In situ hybridization verification revealed that PV was expressed significantly higher throughout the song motor pathway, including brainstem vocal motor neurons relative to the surrounding brain regions of all distantly related avian vocal learners. This differential expression was specific to PV and vocal learners, as it was not found in avian vocal non-learners nor for control genes in learners and non-learners. Similar to the vocal learning birds, higher PV up-regulation was found in the brainstem tongue motor neurons used for speech production in humans relative to a non-human primate, macaques. These results suggest repeated convergent evolution of differential PV up-regulation in the brains of vocal learners separated by more than 65–300 million years from a common ancestor and that the specialized behaviors of learned song and speech may require extra calcium buffering and signaling. Public Library of Science 2012-01-06 /pmc/articles/PMC3253077/ /pubmed/22238614 http://dx.doi.org/10.1371/journal.pone.0029457 Text en Hara 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
Hara, Erina
Rivas, Miriam V.
Ward, James M.
Okanoya, Kazuo
Jarvis, Erich D.
Convergent Differential Regulation of Parvalbumin in the Brains of Vocal Learners
title Convergent Differential Regulation of Parvalbumin in the Brains of Vocal Learners
title_full Convergent Differential Regulation of Parvalbumin in the Brains of Vocal Learners
title_fullStr Convergent Differential Regulation of Parvalbumin in the Brains of Vocal Learners
title_full_unstemmed Convergent Differential Regulation of Parvalbumin in the Brains of Vocal Learners
title_short Convergent Differential Regulation of Parvalbumin in the Brains of Vocal Learners
title_sort convergent differential regulation of parvalbumin in the brains of vocal learners
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253077/
https://www.ncbi.nlm.nih.gov/pubmed/22238614
http://dx.doi.org/10.1371/journal.pone.0029457
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