Transcriptomic and spatial GABAergic neuron subtypes in zona incerta mediate distinct innate behaviors

Understanding the anatomical connection and behaviors of transcriptomic neuron subtypes is critical to delineating cell type-specific functions in the brain. Here we integrated single-nucleus transcriptomic sequencing, in vivo circuit mapping, optogenetic and chemogenetic approaches to dissect the molecular identity and function of heterogeneous GABAergic neuron populations in the zona incerta (ZI) in mice, a region involved in modulating various behaviors. By microdissecting ZI for transcriptomic and spatial gene expression analyses, our results revealed two non-overlapping Ecel1- and Pde11a-expressing GABAergic neurons with dominant expression in the rostral and medial zona incerta (ZIr<sup>Ecel1</sup> and ZIm<sup>Pde11a</sup>), respectively. The GABAergic projection from ZIr<sup>Ecel1</sup> to periaqueductal gray mediates self-grooming, while the GABAergic projection from ZIm<sup>Pde11a</sup> to the oral part of pontine reticular formation promotes transition from sleep to wakefulness. Together, our results revealed the molecular markers, spatial organization and specific neuronal circuits of two discrete GABAergic projection neuron populations in segregated subregions of the ZI that mediate distinct innate behaviors, advancing our understanding of the functional organization of the brain.

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Publication Details

Journal
Nature Communications
Published
2025-04-01
DOI
https://doi.org/10.1038/s41467-025-57896-2
Citations
5
Primary Topic
Neuroinflammation and Neurodegeneration Mechanisms
Type
article
Field-Weighted Citation Impact
4.21

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article

Transcriptomic and spatial GABAergic neuron subtypes in zona incerta mediate distinct innate behaviors

Mengyue Zhu, Xinyue Dai, Yu Zhou, Yan‐Qin Yu et al.
5 citations
Nature Communications
Neuroinflammation and Neurodegeneration Mechanisms
4.21
article

Transcriptomic and spatial GABAergic neuron subtypes in zona incerta mediate distinct innate behaviors

Mengyue Zhu, Xinyue Dai, Yu Zhou, Yan‐Qin Yu, Xiao‐Ming Li, Li Shen, Mi Wang, Huiying Zhang, Jiadong Chen, Jieqiao Peng, Shan Lin, Huiying Zhao
article en
5 citations

Abstract

Understanding the anatomical connection and behaviors of transcriptomic neuron subtypes is critical to delineating cell type-specific functions in the brain. Here we integrated single-nucleus transcriptomic sequencing, in vivo circuit mapping, optogenetic and chemogenetic approaches to dissect the molecular identity and function of heterogeneous GABAergic neuron populations in the zona incerta (ZI) in mice, a region involved in modulating various behaviors. By microdissecting ZI for transcriptomic and spatial gene expression analyses, our results revealed two non-overlapping Ecel1- and Pde11a-expressing GABAergic neurons with dominant expression in the rostral and medial zona incerta (ZIr<sup>Ecel1</sup> and ZIm<sup>Pde11a</sup>), respectively. The GABAergic projection from ZIr<sup>Ecel1</sup> to periaqueductal gray mediates self-grooming, while the GABAergic projection from ZIm<sup>Pde11a</sup> to the oral part of pontine reticular formation promotes transition from sleep to wakefulness. Together, our results revealed the molecular markers, spatial organization and specific neuronal circuits of two discrete GABAergic projection neuron populations in segregated subregions of the ZI that mediate distinct innate behaviors, advancing our understanding of the functional organization of the brain.

Nature CommunicationsVol. 16(1)
Zhejiang Chinese Medical University (CN), Allen Institute for Brain Science (US), Chinese Academy of Medical Sciences & Peking Union Medical College (CN), Interface (United States) (US), Center for Excellence in Brain Science and Intelligence Technology (CN), Zhejiang Lab (CN), Second Affiliated Hospital of Zhejiang University (CN), Shanghai Center for Brain Science and Brain-Inspired Technology (CN), Zhejiang University (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 6%
Neuroinflammation and Neurodegeneration Mechanisms
4.21
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