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Spatial transcriptomic and single-nucleus analysis reveals heterogeneity in a gigantic single-celled syncytium
In multicellular organisms, the specification, coordination, and compartmentalization of cell types enable the formation of complex body plans. However, some eukaryotic protists such as slime molds generate diverse and complex structures while remaining in a multinucleate syncytial state. It is unkn...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8865844/ https://www.ncbi.nlm.nih.gov/pubmed/35195068 http://dx.doi.org/10.7554/eLife.69745 |
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author | Gerber, Tobias Loureiro, Cristina Schramma, Nico Chen, Siyu Jain, Akanksha Weber, Anne Weigert, Anne Santel, Malgorzata Alim, Karen Treutlein, Barbara Camp, J Gray |
author_facet | Gerber, Tobias Loureiro, Cristina Schramma, Nico Chen, Siyu Jain, Akanksha Weber, Anne Weigert, Anne Santel, Malgorzata Alim, Karen Treutlein, Barbara Camp, J Gray |
author_sort | Gerber, Tobias |
collection | PubMed |
description | In multicellular organisms, the specification, coordination, and compartmentalization of cell types enable the formation of complex body plans. However, some eukaryotic protists such as slime molds generate diverse and complex structures while remaining in a multinucleate syncytial state. It is unknown if different regions of these giant syncytial cells have distinct transcriptional responses to environmental encounters and if nuclei within the cell diversify into heterogeneous states. Here, we performed spatial transcriptome analysis of the slime mold Physarum polycephalum in the plasmodium state under different environmental conditions and used single-nucleus RNA-sequencing to dissect gene expression heterogeneity among nuclei. Our data identifies transcriptome regionality in the organism that associates with proliferation, syncytial substructures, and localized environmental conditions. Further, we find that nuclei are heterogenous in their transcriptional profile and may process local signals within the plasmodium to coordinate cell growth, metabolism, and reproduction. To understand how nuclei variation within the syncytium compares to heterogeneity in single-nucleus cells, we analyzed states in single Physarum amoebal cells. We observed amoebal cell states at different stages of mitosis and meiosis, and identified cytokinetic features that are specific to nuclei divisions within the syncytium. Notably, we do not find evidence for predefined transcriptomic states in the amoebae that are observed in the syncytium. Our data shows that a single-celled slime mold can control its gene expression in a region-specific manner while lacking cellular compartmentalization and suggests that nuclei are mobile processors facilitating local specialized functions. More broadly, slime molds offer the extraordinary opportunity to explore how organisms can evolve regulatory mechanisms to divide labor, specialize, balance competition with cooperation, and perform other foundational principles that govern the logic of life. |
format | Online Article Text |
id | pubmed-8865844 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-88658442022-02-24 Spatial transcriptomic and single-nucleus analysis reveals heterogeneity in a gigantic single-celled syncytium Gerber, Tobias Loureiro, Cristina Schramma, Nico Chen, Siyu Jain, Akanksha Weber, Anne Weigert, Anne Santel, Malgorzata Alim, Karen Treutlein, Barbara Camp, J Gray eLife Cell Biology In multicellular organisms, the specification, coordination, and compartmentalization of cell types enable the formation of complex body plans. However, some eukaryotic protists such as slime molds generate diverse and complex structures while remaining in a multinucleate syncytial state. It is unknown if different regions of these giant syncytial cells have distinct transcriptional responses to environmental encounters and if nuclei within the cell diversify into heterogeneous states. Here, we performed spatial transcriptome analysis of the slime mold Physarum polycephalum in the plasmodium state under different environmental conditions and used single-nucleus RNA-sequencing to dissect gene expression heterogeneity among nuclei. Our data identifies transcriptome regionality in the organism that associates with proliferation, syncytial substructures, and localized environmental conditions. Further, we find that nuclei are heterogenous in their transcriptional profile and may process local signals within the plasmodium to coordinate cell growth, metabolism, and reproduction. To understand how nuclei variation within the syncytium compares to heterogeneity in single-nucleus cells, we analyzed states in single Physarum amoebal cells. We observed amoebal cell states at different stages of mitosis and meiosis, and identified cytokinetic features that are specific to nuclei divisions within the syncytium. Notably, we do not find evidence for predefined transcriptomic states in the amoebae that are observed in the syncytium. Our data shows that a single-celled slime mold can control its gene expression in a region-specific manner while lacking cellular compartmentalization and suggests that nuclei are mobile processors facilitating local specialized functions. More broadly, slime molds offer the extraordinary opportunity to explore how organisms can evolve regulatory mechanisms to divide labor, specialize, balance competition with cooperation, and perform other foundational principles that govern the logic of life. eLife Sciences Publications, Ltd 2022-02-23 /pmc/articles/PMC8865844/ /pubmed/35195068 http://dx.doi.org/10.7554/eLife.69745 Text en © 2022, Gerber et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Cell Biology Gerber, Tobias Loureiro, Cristina Schramma, Nico Chen, Siyu Jain, Akanksha Weber, Anne Weigert, Anne Santel, Malgorzata Alim, Karen Treutlein, Barbara Camp, J Gray Spatial transcriptomic and single-nucleus analysis reveals heterogeneity in a gigantic single-celled syncytium |
title | Spatial transcriptomic and single-nucleus analysis reveals heterogeneity in a gigantic single-celled syncytium |
title_full | Spatial transcriptomic and single-nucleus analysis reveals heterogeneity in a gigantic single-celled syncytium |
title_fullStr | Spatial transcriptomic and single-nucleus analysis reveals heterogeneity in a gigantic single-celled syncytium |
title_full_unstemmed | Spatial transcriptomic and single-nucleus analysis reveals heterogeneity in a gigantic single-celled syncytium |
title_short | Spatial transcriptomic and single-nucleus analysis reveals heterogeneity in a gigantic single-celled syncytium |
title_sort | spatial transcriptomic and single-nucleus analysis reveals heterogeneity in a gigantic single-celled syncytium |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8865844/ https://www.ncbi.nlm.nih.gov/pubmed/35195068 http://dx.doi.org/10.7554/eLife.69745 |
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