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A neural circuit mechanism for regulating vocal variability during song learning in zebra finches

Motor skill learning is characterized by improved performance and reduced motor variability. The neural mechanisms that couple skill level and variability, however, are not known. The zebra finch, a songbird, presents a unique opportunity to address this question because production of learned song a...

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Autores principales: Garst-Orozco, Jonathan, Babadi, Baktash, Ölveczky, Bence P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4290448/
https://www.ncbi.nlm.nih.gov/pubmed/25497835
http://dx.doi.org/10.7554/eLife.03697
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author Garst-Orozco, Jonathan
Babadi, Baktash
Ölveczky, Bence P
author_facet Garst-Orozco, Jonathan
Babadi, Baktash
Ölveczky, Bence P
author_sort Garst-Orozco, Jonathan
collection PubMed
description Motor skill learning is characterized by improved performance and reduced motor variability. The neural mechanisms that couple skill level and variability, however, are not known. The zebra finch, a songbird, presents a unique opportunity to address this question because production of learned song and induction of vocal variability are instantiated in distinct circuits that converge on a motor cortex analogue controlling vocal output. To probe the interplay between learning and variability, we made intracellular recordings from neurons in this area, characterizing how their inputs from the functionally distinct pathways change throughout song development. We found that inputs that drive stereotyped song-patterns are strengthened and pruned, while inputs that induce variability remain unchanged. A simple network model showed that strengthening and pruning of action-specific connections reduces the sensitivity of motor control circuits to variable input and neural ‘noise’. This identifies a simple and general mechanism for learning-related regulation of motor variability. DOI: http://dx.doi.org/10.7554/eLife.03697.001
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spelling pubmed-42904482015-01-29 A neural circuit mechanism for regulating vocal variability during song learning in zebra finches Garst-Orozco, Jonathan Babadi, Baktash Ölveczky, Bence P eLife Neuroscience Motor skill learning is characterized by improved performance and reduced motor variability. The neural mechanisms that couple skill level and variability, however, are not known. The zebra finch, a songbird, presents a unique opportunity to address this question because production of learned song and induction of vocal variability are instantiated in distinct circuits that converge on a motor cortex analogue controlling vocal output. To probe the interplay between learning and variability, we made intracellular recordings from neurons in this area, characterizing how their inputs from the functionally distinct pathways change throughout song development. We found that inputs that drive stereotyped song-patterns are strengthened and pruned, while inputs that induce variability remain unchanged. A simple network model showed that strengthening and pruning of action-specific connections reduces the sensitivity of motor control circuits to variable input and neural ‘noise’. This identifies a simple and general mechanism for learning-related regulation of motor variability. DOI: http://dx.doi.org/10.7554/eLife.03697.001 eLife Sciences Publications, Ltd 2014-12-15 /pmc/articles/PMC4290448/ /pubmed/25497835 http://dx.doi.org/10.7554/eLife.03697 Text en © 2014, Garst-Orozco et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Garst-Orozco, Jonathan
Babadi, Baktash
Ölveczky, Bence P
A neural circuit mechanism for regulating vocal variability during song learning in zebra finches
title A neural circuit mechanism for regulating vocal variability during song learning in zebra finches
title_full A neural circuit mechanism for regulating vocal variability during song learning in zebra finches
title_fullStr A neural circuit mechanism for regulating vocal variability during song learning in zebra finches
title_full_unstemmed A neural circuit mechanism for regulating vocal variability during song learning in zebra finches
title_short A neural circuit mechanism for regulating vocal variability during song learning in zebra finches
title_sort neural circuit mechanism for regulating vocal variability during song learning in zebra finches
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4290448/
https://www.ncbi.nlm.nih.gov/pubmed/25497835
http://dx.doi.org/10.7554/eLife.03697
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