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

IF 15.7 1区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES Nature Communications Pub Date : 2025-04-01 DOI:10.1038/s41467-025-57896-2
Mengyue Zhu, Jieqiao Peng, Mi Wang, Shan Lin, Huiying Zhang, Yu Zhou, Xinyue Dai, Huiying Zhao, Yan-qin Yu, Li Shen, Xiao-Ming Li, Jiadong Chen
{"title":"Transcriptomic and spatial GABAergic neuron subtypes in zona incerta mediate distinct innate behaviors","authors":"Mengyue Zhu, Jieqiao Peng, Mi Wang, Shan Lin, Huiying Zhang, Yu Zhou, Xinyue Dai, Huiying Zhao, Yan-qin Yu, Li Shen, Xiao-Ming Li, Jiadong Chen","doi":"10.1038/s41467-025-57896-2","DOIUrl":null,"url":null,"abstract":"<p>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 <i>Ecel1-</i> and <i>Pde11a</i>-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.</p>","PeriodicalId":19066,"journal":{"name":"Nature Communications","volume":"32 1","pages":""},"PeriodicalIF":15.7000,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nature Communications","FirstCategoryId":"103","ListUrlMain":"https://doi.org/10.1038/s41467-025-57896-2","RegionNum":1,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
引用次数: 0

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 (ZIrEcel1 and ZImPde11a), respectively. The GABAergic projection from ZIrEcel1 to periaqueductal gray mediates self-grooming, while the GABAergic projection from ZImPde11a 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.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
无隔带的转录组和空间gaba能神经元亚型介导不同的先天行为
了解转录组神经元亚型的解剖学联系和行为对于描述大脑中细胞类型特异性功能至关重要。在这里,我们整合了单核转录组测序,体内电路作图,光遗传学和化学遗传学方法来解剖小鼠无尾带(ZI)中异质gaba能神经元群体的分子特性和功能,ZI是调节各种行为的区域。通过显微解剖ZI进行转录组学和空间基因表达分析,我们的研究结果揭示了两个不重叠的表达Ecel1-和pde11a的gaba能神经元,分别在喙侧和内侧带(ZIrEcel1和ZImPde11a)占主导地位。从ZIrEcel1到导水管周围灰质的gaba能投射介导自我梳理,而从ZImPde11a到脑桥网状结构的口腔部分的gaba能投射促进从睡眠到清醒的过渡。总之,我们的研究结果揭示了ZI分离亚区中两个离散gaba能投射神经元群体的分子标记、空间组织和特定神经元回路,这些神经元群体介导不同的先天行为,促进了我们对大脑功能组织的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Nature Communications
Nature Communications Biological Science Disciplines-
CiteScore
24.90
自引率
2.40%
发文量
6928
审稿时长
3.7 months
期刊介绍: Nature Communications, an open-access journal, publishes high-quality research spanning all areas of the natural sciences. Papers featured in the journal showcase significant advances relevant to specialists in each respective field. With a 2-year impact factor of 16.6 (2022) and a median time of 8 days from submission to the first editorial decision, Nature Communications is committed to rapid dissemination of research findings. As a multidisciplinary journal, it welcomes contributions from biological, health, physical, chemical, Earth, social, mathematical, applied, and engineering sciences, aiming to highlight important breakthroughs within each domain.
期刊最新文献
Breaking dense integration limits: inverse-designed lithium niobate multimode photonic circuits. Chromatin remodeling factor BAF155 coordinates oligodendroglial-neuronal communications linked to regional myelination and autism-like behavioral deficits in mice Targeted antisense oligonucleotide treatment rescues developmental alterations in spinal muscular atrophy organoids TMEM120A maintains adipose tissue lipid homeostasis through ER CoA channeling HIF-1α-mediated feedback prevents TOR signalling from depleting oxygen supply and triggering stress during normal development
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1