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Differentiation trajectories of the Hydra nervous system reveal transcriptional regulators of neuronal fate

The small freshwater cnidarian polyp Hydra vulgaris uses adult stem cells (interstitial stem cells) to continually replace neurons throughout its life. This feature, combined with the ability to image the entire nervous system (Badhiwala et al., 2021; Dupre & Yuste, 2017) and availability of gen...

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Autores principales: Primack, Abby S, Cazet, Jack F, Little, Hannah Morris, Mühlbauer, Susanne, Cox, Ben D, David, Charles N, Farrell, Jeffrey A, Juliano, Celina E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10055148/
https://www.ncbi.nlm.nih.gov/pubmed/36993575
http://dx.doi.org/10.1101/2023.03.15.531610
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author Primack, Abby S
Cazet, Jack F
Little, Hannah Morris
Mühlbauer, Susanne
Cox, Ben D
David, Charles N
Farrell, Jeffrey A
Juliano, Celina E
author_facet Primack, Abby S
Cazet, Jack F
Little, Hannah Morris
Mühlbauer, Susanne
Cox, Ben D
David, Charles N
Farrell, Jeffrey A
Juliano, Celina E
author_sort Primack, Abby S
collection PubMed
description The small freshwater cnidarian polyp Hydra vulgaris uses adult stem cells (interstitial stem cells) to continually replace neurons throughout its life. This feature, combined with the ability to image the entire nervous system (Badhiwala et al., 2021; Dupre & Yuste, 2017) and availability of gene knockdown techniques (Juliano, Reich, et al., 2014; Lohmann et al., 1999; Vogg et al., 2022), makes Hydra a tractable model for studying nervous system development and regeneration at the whole-organism level. In this study, we use single-cell RNA sequencing and trajectory inference to provide a comprehensive molecular description of the adult nervous system. This includes the most detailed transcriptional characterization of the adult Hydra nervous system to date. We identified eleven unique neuron subtypes together with the transcriptional changes that occur as the interstitial stem cells differentiate into each subtype. Towards the goal of building gene regulatory networks to describe Hydra neuron differentiation, we identified 48 transcription factors expressed specifically in the Hydra nervous system, including many that are conserved regulators of neurogenesis in bilaterians. We also performed ATAC-seq on sorted neurons to uncover previously unidentified putative regulatory regions near neuron-specific genes. Finally, we provide evidence to support the existence of transdifferentiation between mature neuron subtypes and we identify previously unknown transition states in these pathways. All together, we provide a comprehensive transcriptional description of an entire adult nervous system, including differentiation and transdifferentiation pathways, which provides a significant advance towards understanding mechanisms that underlie nervous system regeneration.
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spelling pubmed-100551482023-03-30 Differentiation trajectories of the Hydra nervous system reveal transcriptional regulators of neuronal fate Primack, Abby S Cazet, Jack F Little, Hannah Morris Mühlbauer, Susanne Cox, Ben D David, Charles N Farrell, Jeffrey A Juliano, Celina E bioRxiv Article The small freshwater cnidarian polyp Hydra vulgaris uses adult stem cells (interstitial stem cells) to continually replace neurons throughout its life. This feature, combined with the ability to image the entire nervous system (Badhiwala et al., 2021; Dupre & Yuste, 2017) and availability of gene knockdown techniques (Juliano, Reich, et al., 2014; Lohmann et al., 1999; Vogg et al., 2022), makes Hydra a tractable model for studying nervous system development and regeneration at the whole-organism level. In this study, we use single-cell RNA sequencing and trajectory inference to provide a comprehensive molecular description of the adult nervous system. This includes the most detailed transcriptional characterization of the adult Hydra nervous system to date. We identified eleven unique neuron subtypes together with the transcriptional changes that occur as the interstitial stem cells differentiate into each subtype. Towards the goal of building gene regulatory networks to describe Hydra neuron differentiation, we identified 48 transcription factors expressed specifically in the Hydra nervous system, including many that are conserved regulators of neurogenesis in bilaterians. We also performed ATAC-seq on sorted neurons to uncover previously unidentified putative regulatory regions near neuron-specific genes. Finally, we provide evidence to support the existence of transdifferentiation between mature neuron subtypes and we identify previously unknown transition states in these pathways. All together, we provide a comprehensive transcriptional description of an entire adult nervous system, including differentiation and transdifferentiation pathways, which provides a significant advance towards understanding mechanisms that underlie nervous system regeneration. Cold Spring Harbor Laboratory 2023-04-04 /pmc/articles/PMC10055148/ /pubmed/36993575 http://dx.doi.org/10.1101/2023.03.15.531610 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
Primack, Abby S
Cazet, Jack F
Little, Hannah Morris
Mühlbauer, Susanne
Cox, Ben D
David, Charles N
Farrell, Jeffrey A
Juliano, Celina E
Differentiation trajectories of the Hydra nervous system reveal transcriptional regulators of neuronal fate
title Differentiation trajectories of the Hydra nervous system reveal transcriptional regulators of neuronal fate
title_full Differentiation trajectories of the Hydra nervous system reveal transcriptional regulators of neuronal fate
title_fullStr Differentiation trajectories of the Hydra nervous system reveal transcriptional regulators of neuronal fate
title_full_unstemmed Differentiation trajectories of the Hydra nervous system reveal transcriptional regulators of neuronal fate
title_short Differentiation trajectories of the Hydra nervous system reveal transcriptional regulators of neuronal fate
title_sort differentiation trajectories of the hydra nervous system reveal transcriptional regulators of neuronal fate
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10055148/
https://www.ncbi.nlm.nih.gov/pubmed/36993575
http://dx.doi.org/10.1101/2023.03.15.531610
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