A synaptic locus of song learning
Learning by imitation is the foundation for verbal and musical expression, but its underlying neural basis remains obscure. A juvenile male zebra finch imitates the multisyllabic song of an adult tutor in a process that depends on a song-specialized cortico-basal ganglia circuit, affording a powerful system to identify the synaptic substrates of imitative motor learning. Plasticity at a particular set of cortico-basal ganglia synapses is hypothesized to drive rapid learning-related changes in song before these changes are subsequently consolidated in downstream circuits. Nevertheless, this hypothesis is untested and the synaptic locus where learning initially occurs is unknown. By combining a computational framework to quantify song learning with synapse-specific optogenetic and chemogenetic manipulations within and directly downstream of the cortico-basal ganglia circuit, we identified the specific cortico-basal ganglia synapses that drive the acquisition and expression of rapid vocal changes during juvenile song learning and characterized the hours-long timescale over which these changes consolidate. Furthermore, transiently augmenting postsynaptic activity in the basal ganglia briefly accelerates learning rates and persistently alters song, demonstrating a direct link between basal ganglia activity and rapid learning. These results localize the specific cortico-basal ganglia synapses that enable a juvenile songbird to learn to sing and reveal the circuit logic and behavioral timescales of this imitative learning paradigm. ### Competing Interest Statement The authors have declared no competing interest. National Institutes of Health, K99 NS144525 (DCS), F32 MH132152 (DCS), F31 HD098772 (SB), R01 NS099288 (RM), RF1 NS118424 (RM and JP)
Where does learning through imitation happen in the brain?
In juvenile zebra finches, we pinpoint a synaptic locus of song learning in a cortico-basal ganglia circuit and leverage this localization to measure the timescale of consolidation and make birds learn faster! #neuroskyence (1/14)
21.01.2026 16:39
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What a pleasure to have Prof Sten Grillner form @ki.se visiting us at Kavli Institute for Systems Neuroscience for 2 full days and inspiring us about vertebrate forebrain evolution
24.10.2025 19:44
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๐ Data:
๐ง 36 brains imaged by whole-brain LSFM (shoutout @LifeCanvasTech)
๐ฌ 40 brains imaged with confocal
๐ Anterograde tracing from 8 isocortical areas
๐ Retrograde labeling from 4 brainstem/spinal targets
๐งต More to comeโread the preprint
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25.07.2025 10:46
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We demonstrate how these two neurogenic programsโwith distinct evolutionary historiesโdifferentially shape isocortical output architecture, establishing it as the apex of hierarchical sensorimotor integration.
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25.07.2025 10:46
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This expansion is area-specificโreflecting the functional specialization of each region across motor, sensory, and associative areas.
Itโs shaped by pruning of a pan-isocortex corticospinal axonal scaffold in indirect, but not direct, ET neurons.
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25.07.2025 10:46
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Using novel genetic access to directly- and indirectly-generated extratelencephalic (ET) neurons in the same mouse, we find:
๐ง Direct ET neurons: Project primarily to forebrain & midbrain
๐ง Indirect ET neurons: Amplify these projections and massively expand to hindbrain & spinal cord
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25.07.2025 10:46
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Will start my posts here with a preprint!
First preprint from my postdoctoral workโwhere we redefine and remap the isocortical efferent projectome through two foundational neurogenic mechanisms.
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25.07.2025 10:46
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