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Lineage dynamics of the endosymbiotic cell type in the soft coral Xenia
Many corals harbour symbiotic dinoflagellate algae. The algae live inside coral cells in a specialized membrane compartment known as the symbiosome, which shares the photosynthetically fixed carbon with coral host cells while host cells provide inorganic carbon to the algae for photosynthesis(1). Th...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7332420/ https://www.ncbi.nlm.nih.gov/pubmed/32555454 http://dx.doi.org/10.1038/s41586-020-2385-7 |
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author | Hu, Minjie Zheng, Xiaobin Fan, Chen-Ming Zheng, Yixian |
author_facet | Hu, Minjie Zheng, Xiaobin Fan, Chen-Ming Zheng, Yixian |
author_sort | Hu, Minjie |
collection | PubMed |
description | Many corals harbour symbiotic dinoflagellate algae. The algae live inside coral cells in a specialized membrane compartment known as the symbiosome, which shares the photosynthetically fixed carbon with coral host cells while host cells provide inorganic carbon to the algae for photosynthesis(1). This endosymbiosis—which is critical for the maintenance of coral reef ecosystems—is increasingly threatened by environmental stressors that lead to coral bleaching (that is, the disruption of endosymbiosis), which in turn leads to coral death and the degradation of marine ecosystems(2). The molecular pathways that orchestrate the recognition, uptake and maintenance of algae in coral cells remain poorly understood. Here we report the chromosome-level genome assembly of a Xenia species of fast-growing soft coral(3), and use this species as a model to investigate coral–alga endosymbiosis. Single-cell RNA sequencing identified 16 cell clusters, including gastrodermal cells and cnidocytes, in Xenia sp. We identified the endosymbiotic cell type, which expresses a distinct set of genes that are implicated in the recognition, phagocytosis and/or endocytosis, and maintenance of algae, as well as in the immune modulation of host coral cells. By coupling Xenia sp. regeneration and single-cell RNA sequencing, we observed a dynamic lineage progression of the endosymbiotic cells. The conserved genes associated with endosymbiosis that are reported here may help to reveal common principles by which different corals take up or lose their endosymbionts. |
format | Online Article Text |
id | pubmed-7332420 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-73324202020-07-15 Lineage dynamics of the endosymbiotic cell type in the soft coral Xenia Hu, Minjie Zheng, Xiaobin Fan, Chen-Ming Zheng, Yixian Nature Article Many corals harbour symbiotic dinoflagellate algae. The algae live inside coral cells in a specialized membrane compartment known as the symbiosome, which shares the photosynthetically fixed carbon with coral host cells while host cells provide inorganic carbon to the algae for photosynthesis(1). This endosymbiosis—which is critical for the maintenance of coral reef ecosystems—is increasingly threatened by environmental stressors that lead to coral bleaching (that is, the disruption of endosymbiosis), which in turn leads to coral death and the degradation of marine ecosystems(2). The molecular pathways that orchestrate the recognition, uptake and maintenance of algae in coral cells remain poorly understood. Here we report the chromosome-level genome assembly of a Xenia species of fast-growing soft coral(3), and use this species as a model to investigate coral–alga endosymbiosis. Single-cell RNA sequencing identified 16 cell clusters, including gastrodermal cells and cnidocytes, in Xenia sp. We identified the endosymbiotic cell type, which expresses a distinct set of genes that are implicated in the recognition, phagocytosis and/or endocytosis, and maintenance of algae, as well as in the immune modulation of host coral cells. By coupling Xenia sp. regeneration and single-cell RNA sequencing, we observed a dynamic lineage progression of the endosymbiotic cells. The conserved genes associated with endosymbiosis that are reported here may help to reveal common principles by which different corals take up or lose their endosymbionts. Nature Publishing Group UK 2020-06-17 2020 /pmc/articles/PMC7332420/ /pubmed/32555454 http://dx.doi.org/10.1038/s41586-020-2385-7 Text en © The Author(s) 2020 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/. |
spellingShingle | Article Hu, Minjie Zheng, Xiaobin Fan, Chen-Ming Zheng, Yixian Lineage dynamics of the endosymbiotic cell type in the soft coral Xenia |
title | Lineage dynamics of the endosymbiotic cell type in the soft coral Xenia |
title_full | Lineage dynamics of the endosymbiotic cell type in the soft coral Xenia |
title_fullStr | Lineage dynamics of the endosymbiotic cell type in the soft coral Xenia |
title_full_unstemmed | Lineage dynamics of the endosymbiotic cell type in the soft coral Xenia |
title_short | Lineage dynamics of the endosymbiotic cell type in the soft coral Xenia |
title_sort | lineage dynamics of the endosymbiotic cell type in the soft coral xenia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7332420/ https://www.ncbi.nlm.nih.gov/pubmed/32555454 http://dx.doi.org/10.1038/s41586-020-2385-7 |
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