@article{660f1ab9a52c42c89a6b87c771caf93f,
title = "A Basal Ganglia Circuit Sufficient to Guide Birdsong Learning",
abstract = "Learning vocal behaviors, like speech and birdsong, is thought to rely on continued performance evaluation. Whether candidate performance evaluation circuits in the brain are sufficient to guide vocal learning is not known. Here, we test the sufficiency of VTA projections to the vocal basal ganglia in singing zebra finches, a songbird species that learns to produce a complex and stereotyped multi-syllabic courtship song during development. We optogenetically manipulate VTA axon terminals in singing birds contingent on how the pitch of an individual song syllable is naturally performed. We find that optical inhibition and excitation of VTA terminals are each sufficient to reliably guide learned changes in song. Inhibition and excitation have opponent effects on future performances of targeted song syllables, consistent with positive and negative reinforcement of performance outcomes. These findings define a central role for reinforcement mechanisms in learning vocalizations and demonstrate minimal circuit elements for learning vocal behaviors. Video Abstract: The role of basal ganglia (BG) in learning motor behaviors is poorly understood. Using optogenetic manipulation of axon terminals in singing songbirds, Xiao et al. demonstrate that the ventral tegmental area to BG pathway is sufficient to guide song learning.",
keywords = "basal ganglia, birdsong, dopamine, optogenetics, reinforcement learning, skill learning, songbird, ventral tegmental area, vocal learning, zebra finch",
author = "Lei Xiao and Gaurav Chattree and Oscos, {Francisco Garcia} and Mou Cao and Wanat, {Matthew J.} and Roberts, {Todd F.}",
note = "Funding Information: The authors thank Drs. Joseph Takahashi, Samuel Sober, and Richard Hahnloser and members of the Roberts laboratory for discussions and comments on the manuscript; Dr. Jeremy Clark for advice on fast scanning cyclic voltammetry experiments; Dr. Claire Stelly and Merridee Lefner for fabrication of voltammetry electrodes; Dr. Bence {\"O}lveczky for CAF software; Drs. Karl Deisseroth and Edward Boyden for providing optogenetic constructs; Marguerita Kline for cloning of initial axon-targeted constructs; and Jennifer Holdway and Andrea Guerrero for laboratory support and animal husbandry. The Roberts laboratory was supported by grants from the NIH (R01NS102488, R01DC014364, and R03MH111319), the National Science Foundation (IOS-1457206 and IOS-1451034), University of Texas BRAIN Initiative (362808 and 362430), the Klingenstein-Simons Fellowship, and a NARSAD Young Investigator Grant (Essel Investigator) from the Brain & Behavior Research Foundation (T.F.R.). Funding Information: The authors thank Drs. Joseph Takahashi, Samuel Sober, and Richard Hahnloser and members of the Roberts laboratory for discussions and comments on the manuscript; Dr. Jeremy Clark for advice on fast scanning cyclic voltammetry experiments; Dr. Claire Stelly and Merridee Lefner for fabrication of voltammetry electrodes; Dr. Bence {\"O}lveczky for CAF software; Drs. Karl Deisseroth and Edward Boyden for providing optogenetic constructs; Marguerita Kline for cloning of initial axon-targeted constructs; and Jennifer Holdway and Andrea Guerrero for laboratory support and animal husbandry. The Roberts laboratory was supported by grants from the NIH ( R01NS102488 , R01DC014364 , and R03MH111319 ), the National Science Foundation ( IOS-1457206 and IOS-1451034 ), University of Texas BRAIN Initiative ( 362808 and 362430 ), the Klingenstein-Simons Fellowship , and a NARSAD Young Investigator Grant (Essel Investigator) from the Brain & Behavior Research Foundation (T.F.R.). Publisher Copyright: {\textcopyright} 2018 Elsevier Inc.",
year = "2018",
month = apr,
day = "4",
doi = "10.1016/j.neuron.2018.02.020",
language = "English (US)",
volume = "98",
pages = "208--221.e5",
journal = "Neuron",
issn = "0896-6273",
publisher = "Cell Press",
number = "1",
}