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A molecular atlas of adult C. elegans motor neurons reveals ancient diversity delineated by conserved transcription factor codes
Motor neurons (MNs) constitute an ancient cell type targeted by multiple adult-onset diseases. It is therefore important to define the molecular makeup of adult MNs in animal models and extract organizing principles. Here, we generated a comprehensive molecular atlas of adult Caenorhabditis elegans...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10418256/ https://www.ncbi.nlm.nih.gov/pubmed/37577463 http://dx.doi.org/10.1101/2023.08.04.552048 |
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author | Smith, Jayson J. Taylor, Seth R. Blum, Jacob A. Gitler, Aaron D. Miller, David M. Kratsios, Paschalis |
author_facet | Smith, Jayson J. Taylor, Seth R. Blum, Jacob A. Gitler, Aaron D. Miller, David M. Kratsios, Paschalis |
author_sort | Smith, Jayson J. |
collection | PubMed |
description | Motor neurons (MNs) constitute an ancient cell type targeted by multiple adult-onset diseases. It is therefore important to define the molecular makeup of adult MNs in animal models and extract organizing principles. Here, we generated a comprehensive molecular atlas of adult Caenorhabditis elegans MNs and a searchable database (http://celegans.spinalcordatlas.org). Single-cell RNA-sequencing of 13,200 cells revealed that ventral nerve cord MNs cluster into 29 molecularly distinct subclasses. All subclasses are delineated by unique expression codes of either neuropeptide or transcription factor gene families. Strikingly, we found that combinatorial codes of homeodomain transcription factor genes define adult MN diversity both in C. elegans and mice. Further, molecularly defined MN subclasses in C. elegans display distinct patterns of connectivity. Hence, our study couples the connectivity map of the C. elegans motor circuit with a molecular atlas of its constituent MNs, and uncovers organizing principles and conserved molecular codes of adult MN diversity. |
format | Online Article Text |
id | pubmed-10418256 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-104182562023-08-12 A molecular atlas of adult C. elegans motor neurons reveals ancient diversity delineated by conserved transcription factor codes Smith, Jayson J. Taylor, Seth R. Blum, Jacob A. Gitler, Aaron D. Miller, David M. Kratsios, Paschalis bioRxiv Article Motor neurons (MNs) constitute an ancient cell type targeted by multiple adult-onset diseases. It is therefore important to define the molecular makeup of adult MNs in animal models and extract organizing principles. Here, we generated a comprehensive molecular atlas of adult Caenorhabditis elegans MNs and a searchable database (http://celegans.spinalcordatlas.org). Single-cell RNA-sequencing of 13,200 cells revealed that ventral nerve cord MNs cluster into 29 molecularly distinct subclasses. All subclasses are delineated by unique expression codes of either neuropeptide or transcription factor gene families. Strikingly, we found that combinatorial codes of homeodomain transcription factor genes define adult MN diversity both in C. elegans and mice. Further, molecularly defined MN subclasses in C. elegans display distinct patterns of connectivity. Hence, our study couples the connectivity map of the C. elegans motor circuit with a molecular atlas of its constituent MNs, and uncovers organizing principles and conserved molecular codes of adult MN diversity. Cold Spring Harbor Laboratory 2023-08-06 /pmc/articles/PMC10418256/ /pubmed/37577463 http://dx.doi.org/10.1101/2023.08.04.552048 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Smith, Jayson J. Taylor, Seth R. Blum, Jacob A. Gitler, Aaron D. Miller, David M. Kratsios, Paschalis A molecular atlas of adult C. elegans motor neurons reveals ancient diversity delineated by conserved transcription factor codes |
title | A molecular atlas of adult C. elegans motor neurons reveals ancient diversity delineated by conserved transcription factor codes |
title_full | A molecular atlas of adult C. elegans motor neurons reveals ancient diversity delineated by conserved transcription factor codes |
title_fullStr | A molecular atlas of adult C. elegans motor neurons reveals ancient diversity delineated by conserved transcription factor codes |
title_full_unstemmed | A molecular atlas of adult C. elegans motor neurons reveals ancient diversity delineated by conserved transcription factor codes |
title_short | A molecular atlas of adult C. elegans motor neurons reveals ancient diversity delineated by conserved transcription factor codes |
title_sort | molecular atlas of adult c. elegans motor neurons reveals ancient diversity delineated by conserved transcription factor codes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10418256/ https://www.ncbi.nlm.nih.gov/pubmed/37577463 http://dx.doi.org/10.1101/2023.08.04.552048 |
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