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Zheng, X. M.

Publications and source records attributed to Zheng, X. M..

2 recordsLinked to original sources

Parametric Modulation of a Shared Midbrain Circuit Drives Distinct Vocal Modes in a Singing Mouse

The ability of neural circuits to generate multiple outputs is critical for behavioral flexibility. Here, we leverage the rich vocal behavior of the singing mouse (Scotinomys teguina) to investigate the organizational logic of multifunctional motor circuits. We show that two distinct vocal modes--soft, unstructured ultrasonic vocalizations (USVs) for short-range and loud, rhythmic songs for long-range communication--arise not via parallel pathways but through shared brainstem phonatory circuitry involving the caudolateral periaqueductual gray (clPAG). Using a three-parameter linear model of song rhythm, we demonstrate that synaptic silencing of clPAG progressively alters song duration through a single parameter controlling its termination. This parameter also explains sexual dimorphism in songs, identifying clPAG as a key locus for driving natural behavioral variability. Our findings reveal how parametric modulation of a central circuit node can produce distinct behavioral modes, providing a mechanistic basis for rapid behavioral evolution in mammals.

neuroscience↗

Selective expansion of motor cortical projections in the evolution of vocal novelty

Deciphering how cortical architecture evolves to drive behavioral innovations is a long-standing challenge in neuroscience and evolutionary biology. Here, we leverage a striking behavioral novelty in the Alstons singing mouse (Scotinomys teguina), compared to the laboratory mouse (Mus musculus), to quantitatively test models of motor cortical evolution. We used bulk tracing, serial two-photon tomography, and high-throughput DNA sequencing of over 76,000 barcoded neurons to discover a specific and substantial expansion ([~]200%) of orofacial motor cortical (OMC) projections to the auditory cortical region (AudR) and the midbrain periaqueductal gray (PAG), both implicated in vocal behaviors. Moreover, analysis of individual OMC neurons projection motifs revealed preferential expansion of exclusive projections to AudR. Our results imply that selective expansion of ancestral motor cortical projections can underlie behavioral divergence over short evolutionary timescales, suggesting potential mechanisms for the evolution of enhanced cortical control over vocalizations--a crucial preadaptation for human language.

neuroscience↗