Graded FGF activity patterns distinct cell types within the apical sensory organ of the sea anemone Nematostella vectensis

Bilaterian animals have evolved complex sensory organs comprised of distinct cell types that function coordinately to sense the environment. Each sensory unit has a defined architecture built from component cell types, including sensory cells, non-sensory support cells, and dedicated sensory neurons...

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Veröffentlicht in:Developmental biology 2024-06, Vol.510, p.50-65
Hauptverfasser: Sabin, Keith Z., Chen, Shiyuan, Hill, Eric M., Weaver, Kyle J., Yonke, Jacob, Kirkman, MaryEllen, Redwine, William B., Klompen, Anna M.L., Zhao, Xia, Guo, Fengli, McKinney, Mary Cathleen, Dewey, Jessica L., Gibson, Matthew C.
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container_issue
container_start_page 50
container_title Developmental biology
container_volume 510
creator Sabin, Keith Z.
Chen, Shiyuan
Hill, Eric M.
Weaver, Kyle J.
Yonke, Jacob
Kirkman, MaryEllen
Redwine, William B.
Klompen, Anna M.L.
Zhao, Xia
Guo, Fengli
McKinney, Mary Cathleen
Dewey, Jessica L.
Gibson, Matthew C.
description Bilaterian animals have evolved complex sensory organs comprised of distinct cell types that function coordinately to sense the environment. Each sensory unit has a defined architecture built from component cell types, including sensory cells, non-sensory support cells, and dedicated sensory neurons. Whether this characteristic cellular composition is present in the sensory organs of non-bilaterian animals is unknown. Here, we interrogate the cell type composition and gene regulatory networks controlling development of the larval apical sensory organ in the sea anemone Nematostella vectensis. Using single cell RNA sequencing and imaging approaches, we reveal two unique cell types in the Nematostella apical sensory organ, GABAergic sensory cells and a putative non-sensory support cell population. Further, we identify the paired-like (PRD) homeodomain gene prd146 as a specific sensory cell marker and show that Prd146+ sensory cells become post-mitotic after gastrulation. Genetic loss of function approaches show that Prd146 is essential for apical sensory organ development. Using a candidate gene knockdown approach, we place prd146 downstream of FGF signaling in the apical sensory organ gene regulatory network. Further, we demonstrate that an aboral FGF activity gradient coordinately regulates the specification of both sensory and support cells. Collectively, these experiments define the genetic basis for apical sensory organ development in a non-bilaterian animal and reveal an unanticipated degree of complexity in a prototypic sensory structure. [Display omitted] •The apical sensory organ of Nematostella planulae consist of two distinct cell types.•Prd146 promotes sensory cell specification but represses support cell specification.•The apical sensory organ is not required for the larval to polyp transition in Nematostella.•An aboral FGF activity gradient coordinately specifies sensory and support cells.
doi_str_mv 10.1016/j.ydbio.2024.02.010
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Each sensory unit has a defined architecture built from component cell types, including sensory cells, non-sensory support cells, and dedicated sensory neurons. Whether this characteristic cellular composition is present in the sensory organs of non-bilaterian animals is unknown. Here, we interrogate the cell type composition and gene regulatory networks controlling development of the larval apical sensory organ in the sea anemone Nematostella vectensis. Using single cell RNA sequencing and imaging approaches, we reveal two unique cell types in the Nematostella apical sensory organ, GABAergic sensory cells and a putative non-sensory support cell population. Further, we identify the paired-like (PRD) homeodomain gene prd146 as a specific sensory cell marker and show that Prd146+ sensory cells become post-mitotic after gastrulation. Genetic loss of function approaches show that Prd146 is essential for apical sensory organ development. Using a candidate gene knockdown approach, we place prd146 downstream of FGF signaling in the apical sensory organ gene regulatory network. Further, we demonstrate that an aboral FGF activity gradient coordinately regulates the specification of both sensory and support cells. Collectively, these experiments define the genetic basis for apical sensory organ development in a non-bilaterian animal and reveal an unanticipated degree of complexity in a prototypic sensory structure. [Display omitted] •The apical sensory organ of Nematostella planulae consist of two distinct cell types.•Prd146 promotes sensory cell specification but represses support cell specification.•The apical sensory organ is not required for the larval to polyp transition in Nematostella.•An aboral FGF activity gradient coordinately specifies sensory and support cells.</description><identifier>ISSN: 0012-1606</identifier><identifier>EISSN: 1095-564X</identifier><identifier>DOI: 10.1016/j.ydbio.2024.02.010</identifier><identifier>PMID: 38521499</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Apical sensory organs ; Cell type specification ; Larva ; Nematostella vectensis ; Single cell RNA-Sequencing ; Transcription factors</subject><ispartof>Developmental biology, 2024-06, Vol.510, p.50-65</ispartof><rights>2024 The Authors</rights><rights>Copyright © 2024 The Authors. Published by Elsevier Inc. 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Using a candidate gene knockdown approach, we place prd146 downstream of FGF signaling in the apical sensory organ gene regulatory network. Further, we demonstrate that an aboral FGF activity gradient coordinately regulates the specification of both sensory and support cells. Collectively, these experiments define the genetic basis for apical sensory organ development in a non-bilaterian animal and reveal an unanticipated degree of complexity in a prototypic sensory structure. 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subjects Apical sensory organs
Cell type specification
Larva
Nematostella vectensis
Single cell RNA-Sequencing
Transcription factors
title Graded FGF activity patterns distinct cell types within the apical sensory organ of the sea anemone Nematostella vectensis
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