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Single-cell atavism reveals an ancient mechanism of cell type diversification in a sea anemone
Cnidocytes are the explosive stinging cells unique to cnidarians (corals, jellyfish, etc). Specialized for prey capture and defense, cnidocytes comprise a group of over 30 morphologically and functionally distinct cell types. These unusual cells are iconic examples of biological novelty but the deve...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9935875/ https://www.ncbi.nlm.nih.gov/pubmed/36797294 http://dx.doi.org/10.1038/s41467-023-36615-9 |
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author | Babonis, Leslie S. Enjolras, Camille Reft, Abigail J. Foster, Brent M. Hugosson, Fredrik Ryan, Joseph F. Daly, Marymegan Martindale, Mark Q. |
author_facet | Babonis, Leslie S. Enjolras, Camille Reft, Abigail J. Foster, Brent M. Hugosson, Fredrik Ryan, Joseph F. Daly, Marymegan Martindale, Mark Q. |
author_sort | Babonis, Leslie S. |
collection | PubMed |
description | Cnidocytes are the explosive stinging cells unique to cnidarians (corals, jellyfish, etc). Specialized for prey capture and defense, cnidocytes comprise a group of over 30 morphologically and functionally distinct cell types. These unusual cells are iconic examples of biological novelty but the developmental mechanisms driving diversity of the stinging apparatus are poorly characterized, making it challenging to understand the evolutionary history of stinging cells. Using CRISPR/Cas9-mediated genome editing in the sea anemone Nematostella vectensis, we show that a single transcription factor (NvSox2) acts as a binary switch between two alternative stinging cell fates. Knockout of NvSox2 causes a transformation of piercing cells into ensnaring cells, which are common in other species of sea anemone but appear to have been silenced in N. vectensis. These results reveal an unusual case of single-cell atavism and expand our understanding of the diversification of cell type identity. |
format | Online Article Text |
id | pubmed-9935875 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-99358752023-02-18 Single-cell atavism reveals an ancient mechanism of cell type diversification in a sea anemone Babonis, Leslie S. Enjolras, Camille Reft, Abigail J. Foster, Brent M. Hugosson, Fredrik Ryan, Joseph F. Daly, Marymegan Martindale, Mark Q. Nat Commun Article Cnidocytes are the explosive stinging cells unique to cnidarians (corals, jellyfish, etc). Specialized for prey capture and defense, cnidocytes comprise a group of over 30 morphologically and functionally distinct cell types. These unusual cells are iconic examples of biological novelty but the developmental mechanisms driving diversity of the stinging apparatus are poorly characterized, making it challenging to understand the evolutionary history of stinging cells. Using CRISPR/Cas9-mediated genome editing in the sea anemone Nematostella vectensis, we show that a single transcription factor (NvSox2) acts as a binary switch between two alternative stinging cell fates. Knockout of NvSox2 causes a transformation of piercing cells into ensnaring cells, which are common in other species of sea anemone but appear to have been silenced in N. vectensis. These results reveal an unusual case of single-cell atavism and expand our understanding of the diversification of cell type identity. Nature Publishing Group UK 2023-02-16 /pmc/articles/PMC9935875/ /pubmed/36797294 http://dx.doi.org/10.1038/s41467-023-36615-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Babonis, Leslie S. Enjolras, Camille Reft, Abigail J. Foster, Brent M. Hugosson, Fredrik Ryan, Joseph F. Daly, Marymegan Martindale, Mark Q. Single-cell atavism reveals an ancient mechanism of cell type diversification in a sea anemone |
title | Single-cell atavism reveals an ancient mechanism of cell type diversification in a sea anemone |
title_full | Single-cell atavism reveals an ancient mechanism of cell type diversification in a sea anemone |
title_fullStr | Single-cell atavism reveals an ancient mechanism of cell type diversification in a sea anemone |
title_full_unstemmed | Single-cell atavism reveals an ancient mechanism of cell type diversification in a sea anemone |
title_short | Single-cell atavism reveals an ancient mechanism of cell type diversification in a sea anemone |
title_sort | single-cell atavism reveals an ancient mechanism of cell type diversification in a sea anemone |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9935875/ https://www.ncbi.nlm.nih.gov/pubmed/36797294 http://dx.doi.org/10.1038/s41467-023-36615-9 |
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