Unknown

Dataset Information

0

Comprehensive analysis of cellular specializations that initiate parallel auditory processing pathways in mice.


ABSTRACT: The cochlear nuclear complex (CN) is the starting point for all central auditory processing and comprises a suite of neuronal cell types that are highly specialized for neural coding of acoustic signals. To examine how their striking functional specializations are determined at the molecular level, we performed single-nucleus RNA sequencing of the mouse CN to molecularly define all constituent cell types and related them to morphologically- and electrophysiologically-defined neurons using Patch-seq. We reveal an expanded set of molecular cell types encompassing all previously described major types and discover new subtypes both in terms of topographic and cell-physiologic properties. Our results define a complete cell-type taxonomy in CN that reconciles anatomical position, morphological, physiological, and molecular criteria. This high-resolution account of cellular heterogeneity and specializations from the molecular to the circuit level illustrates molecular underpinnings of functional specializations and enables genetic dissection of auditory processing and hearing disorders with unprecedented specificity.

SUBMITTER: Jing J 

PROVIDER: S-EPMC10245571 | biostudies-literature | 2023 Oct

REPOSITORIES: biostudies-literature

altmetric image

Publications

Molecular logic for cellular specializations that initiate the auditory parallel processing pathways.

Jing Junzhan J   Hu Ming M   Ngodup Tenzin T   Ma Qianqian Q   Lau Shu-Ning Natalie SN   Ljungberg Cecilia C   McGinley Matthew J MJ   Trussell Laurence O LO   Jiang Xiaolong X  

bioRxiv : the preprint server for biology 20241006


The cochlear nuclear complex (CN), the starting point for all central auditory processing, comprises a suite of neuronal cell types that are highly specialized for neural coding of acoustic signals, yet molecular logic governing cellular specializations remains unknown. By combining single-nucleus RNA sequencing and Patch-seq analysis, we reveal a set of transcriptionally distinct cell populations encompassing all previously observed types and discover multiple new subtypes with anatomical and p  ...[more]

Similar Datasets

2024-11-04 | GSE273145 | GEO
| S-EPMC6384027 | biostudies-literature
| S-EPMC6245510 | biostudies-other
| S-EPMC6215474 | biostudies-literature
| S-EPMC9671866 | biostudies-literature
| S-EPMC5418552 | biostudies-literature
| S-EPMC3415711 | biostudies-other
| S-EPMC2842045 | biostudies-literature
| S-EPMC6852359 | biostudies-literature
| S-EPMC5364438 | biostudies-literature