Cargando…

Urotensin-related gene transcripts mark developmental emergence of the male forebrain vocal control system in songbirds

Songbirds communicate through learned vocalizations, using a forebrain circuit with convergent similarity to vocal-control circuitry in humans. This circuit is incomplete in female zebra finches, hence only males sing. We show that the UTS2B gene, encoding Urotensin-Related Peptide (URP), is uniquel...

Descripción completa

Detalles Bibliográficos
Autores principales: Bell, Zachary W., Lovell, Peter, Mello, Claudio V., Yip, Ping K., George, Julia M., Clayton, David F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6349858/
https://www.ncbi.nlm.nih.gov/pubmed/30692609
http://dx.doi.org/10.1038/s41598-018-37057-w
_version_ 1783390334975213568
author Bell, Zachary W.
Lovell, Peter
Mello, Claudio V.
Yip, Ping K.
George, Julia M.
Clayton, David F.
author_facet Bell, Zachary W.
Lovell, Peter
Mello, Claudio V.
Yip, Ping K.
George, Julia M.
Clayton, David F.
author_sort Bell, Zachary W.
collection PubMed
description Songbirds communicate through learned vocalizations, using a forebrain circuit with convergent similarity to vocal-control circuitry in humans. This circuit is incomplete in female zebra finches, hence only males sing. We show that the UTS2B gene, encoding Urotensin-Related Peptide (URP), is uniquely expressed in a key pre-motor vocal nucleus (HVC), and specifically marks the neurons that form a male-specific projection that encodes timing features of learned song. UTS2B-expressing cells appear early in males, prior to projection formation, but are not observed in the female nucleus. We find no expression evidence for canonical receptors within the vocal circuit, suggesting either signalling to other brain regions via diffusion or transduction through other receptor systems. Urotensins have not previously been implicated in vocal control, but we find an annotation in Allen Human Brain Atlas of increased UTS2B expression within portions of human inferior frontal cortex implicated in human speech and singing. Thus UTS2B (URP) is a novel neural marker that may have conserved functions for vocal communication.
format Online
Article
Text
id pubmed-6349858
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-63498582019-01-30 Urotensin-related gene transcripts mark developmental emergence of the male forebrain vocal control system in songbirds Bell, Zachary W. Lovell, Peter Mello, Claudio V. Yip, Ping K. George, Julia M. Clayton, David F. Sci Rep Article Songbirds communicate through learned vocalizations, using a forebrain circuit with convergent similarity to vocal-control circuitry in humans. This circuit is incomplete in female zebra finches, hence only males sing. We show that the UTS2B gene, encoding Urotensin-Related Peptide (URP), is uniquely expressed in a key pre-motor vocal nucleus (HVC), and specifically marks the neurons that form a male-specific projection that encodes timing features of learned song. UTS2B-expressing cells appear early in males, prior to projection formation, but are not observed in the female nucleus. We find no expression evidence for canonical receptors within the vocal circuit, suggesting either signalling to other brain regions via diffusion or transduction through other receptor systems. Urotensins have not previously been implicated in vocal control, but we find an annotation in Allen Human Brain Atlas of increased UTS2B expression within portions of human inferior frontal cortex implicated in human speech and singing. Thus UTS2B (URP) is a novel neural marker that may have conserved functions for vocal communication. Nature Publishing Group UK 2019-01-28 /pmc/articles/PMC6349858/ /pubmed/30692609 http://dx.doi.org/10.1038/s41598-018-37057-w Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Bell, Zachary W.
Lovell, Peter
Mello, Claudio V.
Yip, Ping K.
George, Julia M.
Clayton, David F.
Urotensin-related gene transcripts mark developmental emergence of the male forebrain vocal control system in songbirds
title Urotensin-related gene transcripts mark developmental emergence of the male forebrain vocal control system in songbirds
title_full Urotensin-related gene transcripts mark developmental emergence of the male forebrain vocal control system in songbirds
title_fullStr Urotensin-related gene transcripts mark developmental emergence of the male forebrain vocal control system in songbirds
title_full_unstemmed Urotensin-related gene transcripts mark developmental emergence of the male forebrain vocal control system in songbirds
title_short Urotensin-related gene transcripts mark developmental emergence of the male forebrain vocal control system in songbirds
title_sort urotensin-related gene transcripts mark developmental emergence of the male forebrain vocal control system in songbirds
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6349858/
https://www.ncbi.nlm.nih.gov/pubmed/30692609
http://dx.doi.org/10.1038/s41598-018-37057-w
work_keys_str_mv AT bellzacharyw urotensinrelatedgenetranscriptsmarkdevelopmentalemergenceofthemaleforebrainvocalcontrolsysteminsongbirds
AT lovellpeter urotensinrelatedgenetranscriptsmarkdevelopmentalemergenceofthemaleforebrainvocalcontrolsysteminsongbirds
AT melloclaudiov urotensinrelatedgenetranscriptsmarkdevelopmentalemergenceofthemaleforebrainvocalcontrolsysteminsongbirds
AT yippingk urotensinrelatedgenetranscriptsmarkdevelopmentalemergenceofthemaleforebrainvocalcontrolsysteminsongbirds
AT georgejuliam urotensinrelatedgenetranscriptsmarkdevelopmentalemergenceofthemaleforebrainvocalcontrolsysteminsongbirds
AT claytondavidf urotensinrelatedgenetranscriptsmarkdevelopmentalemergenceofthemaleforebrainvocalcontrolsysteminsongbirds