Literature DB >> 22015923

A hypothesis for basal ganglia-dependent reinforcement learning in the songbird.

M S Fee1, J H Goldberg.   

Abstract

Most of our motor skills are not innately programmed, but are learned by a combination of motor exploration and performance evaluation, suggesting that they proceed through a reinforcement learning (RL) mechanism. Songbirds have emerged as a model system to study how a complex behavioral sequence can be learned through an RL-like strategy. Interestingly, like motor sequence learning in mammals, song learning in birds requires a basal ganglia (BG)-thalamocortical loop, suggesting common neural mechanisms. Here, we outline a specific working hypothesis for how BG-forebrain circuits could utilize an internally computed reinforcement signal to direct song learning. Our model includes a number of general concepts borrowed from the mammalian BG literature, including a dopaminergic reward prediction error and dopamine-mediated plasticity at corticostriatal synapses. We also invoke a number of conceptual advances arising from recent observations in the songbird. Specifically, there is evidence for a specialized cortical circuit that adds trial-to-trial variability to stereotyped cortical motor programs, and a role for the BG in "biasing" this variability to improve behavioral performance. This BG-dependent "premotor bias" may in turn guide plasticity in downstream cortical synapses to consolidate recently learned song changes. Given the similarity between mammalian and songbird BG-thalamocortical circuits, our model for the role of the BG in this process may have broader relevance to mammalian BG function.
Copyright © 2011 IBRO. Published by Elsevier Ltd. All rights reserved.

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Year:  2011        PMID: 22015923      PMCID: PMC3221789          DOI: 10.1016/j.neuroscience.2011.09.069

Source DB:  PubMed          Journal:  Neuroscience        ISSN: 0306-4522            Impact factor:   3.590


  178 in total

1.  Temporal sparseness of the premotor drive is important for rapid learning in a neural network model of birdsong.

Authors:  Ila R Fiete; Richard H R Hahnloser; Michale S Fee; H Sebastian Seung
Journal:  J Neurophysiol       Date:  2004-04-07       Impact factor: 2.714

2.  Distributed but convergent ordering of corticostriatal projections: analysis of the frontal eye field and the supplementary eye field in the macaque monkey.

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Journal:  J Neurosci       Date:  1992-11       Impact factor: 6.167

3.  For whom the bird sings: context-dependent gene expression.

Authors:  E D Jarvis; C Scharff; M R Grossman; J A Ramos; F Nottebohm
Journal:  Neuron       Date:  1998-10       Impact factor: 17.173

Review 4.  A neural substrate of prediction and reward.

Authors:  W Schultz; P Dayan; P R Montague
Journal:  Science       Date:  1997-03-14       Impact factor: 47.728

5.  Neurotrophins suppress apoptosis induced by deafferentation of an avian motor-cortical region.

Authors:  F Johnson; S E Hohmann; P S DiStefano; S W Bottjer
Journal:  J Neurosci       Date:  1997-03-15       Impact factor: 6.167

6.  Differential perikaryal localization in rats of D1 and D2 dopamine receptors on striatal projection neuron types identified by retrograde labeling.

Authors:  Yun-Ping Deng; Wan-Long Lei; Anton Reiner
Journal:  J Chem Neuroanat       Date:  2006-08-17       Impact factor: 3.052

Review 7.  Distributed modular architectures linking basal ganglia, cerebellum, and cerebral cortex: their role in planning and controlling action.

Authors:  J C Houk; S P Wise
Journal:  Cereb Cortex       Date:  1995 Mar-Apr       Impact factor: 5.357

Review 8.  Neural pathways for the control of birdsong production.

Authors:  J M Wild
Journal:  J Neurobiol       Date:  1997-11

Review 9.  Dopamine and synaptic plasticity in dorsal striatal circuits controlling action selection.

Authors:  D James Surmeier; Joshua Plotkin; Weixing Shen
Journal:  Curr Opin Neurobiol       Date:  2009-11-05       Impact factor: 6.627

10.  Learning the microstructure of successful behavior.

Authors:  Jonathan D Charlesworth; Evren C Tumer; Timothy L Warren; Michael S Brainard
Journal:  Nat Neurosci       Date:  2011-01-30       Impact factor: 24.884

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  90 in total

1.  Integration of cortical and pallidal inputs in the basal ganglia-recipient thalamus of singing birds.

Authors:  Jesse H Goldberg; Michael A Farries; Michale S Fee
Journal:  J Neurophysiol       Date:  2012-06-06       Impact factor: 2.714

Review 2.  The role of efference copy in striatal learning.

Authors:  Michale S Fee
Journal:  Curr Opin Neurobiol       Date:  2014-02-21       Impact factor: 6.627

3.  Origins of basal ganglia output signals in singing juvenile birds.

Authors:  Morgane Pidoux; Tejapratap Bollu; Tori Riccelli; Jesse H Goldberg
Journal:  J Neurophysiol       Date:  2014-11-12       Impact factor: 2.714

4.  The Avian Basal Ganglia Are a Source of Rapid Behavioral Variation That Enables Vocal Motor Exploration.

Authors:  Satoshi Kojima; Mimi H Kao; Allison J Doupe; Michael S Brainard
Journal:  J Neurosci       Date:  2018-09-24       Impact factor: 6.167

Review 5.  Auditory-vocal mirroring in songbirds.

Authors:  Richard Mooney
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2014-04-28       Impact factor: 6.237

6.  A Basal Ganglia Circuit Sufficient to Guide Birdsong Learning.

Authors:  Lei Xiao; Gaurav Chattree; Francisco Garcia Oscos; Mou Cao; Matthew J Wanat; Todd F Roberts
Journal:  Neuron       Date:  2018-03-15       Impact factor: 17.173

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

Authors:  Jonathan Garst-Orozco; Baktash Babadi; Bence P Ölveczky
Journal:  Elife       Date:  2014-12-15       Impact factor: 8.140

8.  A role for descending auditory cortical projections in songbird vocal learning.

Authors:  Yael Mandelblat-Cerf; Liora Las; Natalia Denisenko; Michale S Fee
Journal:  Elife       Date:  2014-06-16       Impact factor: 8.140

9.  Dopamine neurons encode performance error in singing birds.

Authors:  Vikram Gadagkar; Pavel A Puzerey; Ruidong Chen; Eliza Baird-Daniel; Alexander R Farhang; Jesse H Goldberg
Journal:  Science       Date:  2016-12-08       Impact factor: 47.728

10.  Punishment-induced behavioral and neurophysiological variability reveals dopamine-dependent selection of kinematic movement parameters.

Authors:  Joseph M Galea; Diane Ruge; Arthur Buijink; Sven Bestmann; John C Rothwell
Journal:  J Neurosci       Date:  2013-02-27       Impact factor: 6.167

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