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Single-cell RNAseq analysis of spinal locomotor circuitry in larval zebrafish

Identification of the neuronal types that form the specialized circuits controlling distinct behaviors has benefited greatly from the simplicity offered by zebrafish. Electrophysiological studies have shown that in addition to connectivity, understanding of circuitry requires identification of funct...

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Detalles Bibliográficos
Autores principales: Kelly, Jimmy J, Wen, Hua, Brehm, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10656102/
https://www.ncbi.nlm.nih.gov/pubmed/37975797
http://dx.doi.org/10.7554/eLife.89338
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author Kelly, Jimmy J
Wen, Hua
Brehm, Paul
author_facet Kelly, Jimmy J
Wen, Hua
Brehm, Paul
author_sort Kelly, Jimmy J
collection PubMed
description Identification of the neuronal types that form the specialized circuits controlling distinct behaviors has benefited greatly from the simplicity offered by zebrafish. Electrophysiological studies have shown that in addition to connectivity, understanding of circuitry requires identification of functional specializations among individual circuit components, such as those that regulate levels of transmitter release and neuronal excitability. In this study, we use single-cell RNA sequencing (scRNAseq) to identify the molecular bases for functional distinctions between motoneuron types that are causal to their differential roles in swimming. The primary motoneuron, in particular, expresses high levels of a unique combination of voltage-dependent ion channel types and synaptic proteins termed functional ‘cassettes.’ The ion channel types are specialized for promoting high-frequency firing of action potentials and augmented transmitter release at the neuromuscular junction, both contributing to greater power generation. Our transcriptional profiling of spinal neurons further assigns expression of this cassette to specific interneuron types also involved in the central circuitry controlling high-speed swimming and escape behaviors. Our analysis highlights the utility of scRNAseq in functional characterization of neuronal circuitry, in addition to providing a gene expression resource for studying cell type diversity.
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spelling pubmed-106561022023-11-17 Single-cell RNAseq analysis of spinal locomotor circuitry in larval zebrafish Kelly, Jimmy J Wen, Hua Brehm, Paul eLife Neuroscience Identification of the neuronal types that form the specialized circuits controlling distinct behaviors has benefited greatly from the simplicity offered by zebrafish. Electrophysiological studies have shown that in addition to connectivity, understanding of circuitry requires identification of functional specializations among individual circuit components, such as those that regulate levels of transmitter release and neuronal excitability. In this study, we use single-cell RNA sequencing (scRNAseq) to identify the molecular bases for functional distinctions between motoneuron types that are causal to their differential roles in swimming. The primary motoneuron, in particular, expresses high levels of a unique combination of voltage-dependent ion channel types and synaptic proteins termed functional ‘cassettes.’ The ion channel types are specialized for promoting high-frequency firing of action potentials and augmented transmitter release at the neuromuscular junction, both contributing to greater power generation. Our transcriptional profiling of spinal neurons further assigns expression of this cassette to specific interneuron types also involved in the central circuitry controlling high-speed swimming and escape behaviors. Our analysis highlights the utility of scRNAseq in functional characterization of neuronal circuitry, in addition to providing a gene expression resource for studying cell type diversity. eLife Sciences Publications, Ltd 2023-11-17 /pmc/articles/PMC10656102/ /pubmed/37975797 http://dx.doi.org/10.7554/eLife.89338 Text en © 2023, Kelly, Wen et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Kelly, Jimmy J
Wen, Hua
Brehm, Paul
Single-cell RNAseq analysis of spinal locomotor circuitry in larval zebrafish
title Single-cell RNAseq analysis of spinal locomotor circuitry in larval zebrafish
title_full Single-cell RNAseq analysis of spinal locomotor circuitry in larval zebrafish
title_fullStr Single-cell RNAseq analysis of spinal locomotor circuitry in larval zebrafish
title_full_unstemmed Single-cell RNAseq analysis of spinal locomotor circuitry in larval zebrafish
title_short Single-cell RNAseq analysis of spinal locomotor circuitry in larval zebrafish
title_sort single-cell rnaseq analysis of spinal locomotor circuitry in larval zebrafish
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10656102/
https://www.ncbi.nlm.nih.gov/pubmed/37975797
http://dx.doi.org/10.7554/eLife.89338
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