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A single-cell atlas reveals unanticipated cell type complexity in Drosophila ovaries
Organ function relies on the spatial organization and functional coordination of numerous cell types. The Drosophila ovary is a widely used model system to study the cellular activities underlying organ function, including stem cell regulation, cell signaling and epithelial morphogenesis. However, t...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8494228/ https://www.ncbi.nlm.nih.gov/pubmed/34389661 http://dx.doi.org/10.1101/gr.274340.120 |
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author | Slaidina, Maija Gupta, Selena Banisch, Torsten U. Lehmann, Ruth |
author_facet | Slaidina, Maija Gupta, Selena Banisch, Torsten U. Lehmann, Ruth |
author_sort | Slaidina, Maija |
collection | PubMed |
description | Organ function relies on the spatial organization and functional coordination of numerous cell types. The Drosophila ovary is a widely used model system to study the cellular activities underlying organ function, including stem cell regulation, cell signaling and epithelial morphogenesis. However, the relative paucity of cell type–specific reagents hinders investigation of molecular functions at the appropriate cellular resolution. Here, we used single-cell RNA sequencing to characterize all cell types of the stem cell compartment and early follicles of the Drosophila ovary. We computed transcriptional signatures and identified specific markers for nine states of germ cell differentiation and 23 somatic cell types and subtypes. We uncovered an unanticipated diversity of escort cells, the somatic cells that directly interact with differentiating germline cysts. Three escort cell subtypes reside in discrete anatomical positions and express distinct sets of secreted and transmembrane proteins, suggesting that diverse micro-environments support the progressive differentiation of germ cells. Finally, we identified 17 follicle cell subtypes and characterized their transcriptional profiles. Altogether, we provide a comprehensive resource of gene expression, cell type–specific markers, spatial coordinates, and functional predictions for 34 ovarian cell types and subtypes. |
format | Online Article Text |
id | pubmed-8494228 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-84942282021-10-07 A single-cell atlas reveals unanticipated cell type complexity in Drosophila ovaries Slaidina, Maija Gupta, Selena Banisch, Torsten U. Lehmann, Ruth Genome Res Resource Organ function relies on the spatial organization and functional coordination of numerous cell types. The Drosophila ovary is a widely used model system to study the cellular activities underlying organ function, including stem cell regulation, cell signaling and epithelial morphogenesis. However, the relative paucity of cell type–specific reagents hinders investigation of molecular functions at the appropriate cellular resolution. Here, we used single-cell RNA sequencing to characterize all cell types of the stem cell compartment and early follicles of the Drosophila ovary. We computed transcriptional signatures and identified specific markers for nine states of germ cell differentiation and 23 somatic cell types and subtypes. We uncovered an unanticipated diversity of escort cells, the somatic cells that directly interact with differentiating germline cysts. Three escort cell subtypes reside in discrete anatomical positions and express distinct sets of secreted and transmembrane proteins, suggesting that diverse micro-environments support the progressive differentiation of germ cells. Finally, we identified 17 follicle cell subtypes and characterized their transcriptional profiles. Altogether, we provide a comprehensive resource of gene expression, cell type–specific markers, spatial coordinates, and functional predictions for 34 ovarian cell types and subtypes. Cold Spring Harbor Laboratory Press 2021-10 /pmc/articles/PMC8494228/ /pubmed/34389661 http://dx.doi.org/10.1101/gr.274340.120 Text en © 2021 Slaidina et al.; Published by Cold Spring Harbor Laboratory Press https://creativecommons.org/licenses/by-nc/4.0/This article, published in Genome Research, is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Resource Slaidina, Maija Gupta, Selena Banisch, Torsten U. Lehmann, Ruth A single-cell atlas reveals unanticipated cell type complexity in Drosophila ovaries |
title | A single-cell atlas reveals unanticipated cell type complexity in Drosophila ovaries |
title_full | A single-cell atlas reveals unanticipated cell type complexity in Drosophila ovaries |
title_fullStr | A single-cell atlas reveals unanticipated cell type complexity in Drosophila ovaries |
title_full_unstemmed | A single-cell atlas reveals unanticipated cell type complexity in Drosophila ovaries |
title_short | A single-cell atlas reveals unanticipated cell type complexity in Drosophila ovaries |
title_sort | single-cell atlas reveals unanticipated cell type complexity in drosophila ovaries |
topic | Resource |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8494228/ https://www.ncbi.nlm.nih.gov/pubmed/34389661 http://dx.doi.org/10.1101/gr.274340.120 |
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