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Single cell RNA-seq 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 additional to connectivity, understanding of circuitry requires identification of functi...

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Autores principales: Kelly, Jimmy J., Wen, Hua, Brehm, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10274715/
https://www.ncbi.nlm.nih.gov/pubmed/37333232
http://dx.doi.org/10.1101/2023.06.06.543939
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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 additional 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 (PMn) 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-102747152023-06-17 Single cell RNA-seq analysis of spinal locomotor circuitry in larval zebrafish Kelly, Jimmy J. Wen, Hua Brehm, Paul bioRxiv Article 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 additional 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 (PMn) 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. Cold Spring Harbor Laboratory 2023-09-14 /pmc/articles/PMC10274715/ /pubmed/37333232 http://dx.doi.org/10.1101/2023.06.06.543939 Text en https://creativecommons.org/licenses/by-nd/4.0/This work is licensed under a Creative Commons Attribution-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, and only so long as attribution is given to the creator. The license allows for commercial use.
spellingShingle Article
Kelly, Jimmy J.
Wen, Hua
Brehm, Paul
Single cell RNA-seq analysis of spinal locomotor circuitry in larval zebrafish
title Single cell RNA-seq analysis of spinal locomotor circuitry in larval zebrafish
title_full Single cell RNA-seq analysis of spinal locomotor circuitry in larval zebrafish
title_fullStr Single cell RNA-seq analysis of spinal locomotor circuitry in larval zebrafish
title_full_unstemmed Single cell RNA-seq analysis of spinal locomotor circuitry in larval zebrafish
title_short Single cell RNA-seq analysis of spinal locomotor circuitry in larval zebrafish
title_sort single cell rna-seq analysis of spinal locomotor circuitry in larval zebrafish
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10274715/
https://www.ncbi.nlm.nih.gov/pubmed/37333232
http://dx.doi.org/10.1101/2023.06.06.543939
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