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A cellular and molecular atlas reveals the basis of chytrid development
The chytrids (phylum Chytridiomycota) are a major fungal lineage of ecological and evolutionary importance. Despite their importance, many fundamental aspects of chytrid developmental and cell biology remain poorly understood. To address these knowledge gaps, we combined quantitative volume electron...
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/PMC8887899/ https://www.ncbi.nlm.nih.gov/pubmed/35227375 http://dx.doi.org/10.7554/eLife.73933 |
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author | Laundon, Davis Chrismas, Nathan Bird, Kimberley Thomas, Seth Mock, Thomas Cunliffe, Michael |
author_facet | Laundon, Davis Chrismas, Nathan Bird, Kimberley Thomas, Seth Mock, Thomas Cunliffe, Michael |
author_sort | Laundon, Davis |
collection | PubMed |
description | The chytrids (phylum Chytridiomycota) are a major fungal lineage of ecological and evolutionary importance. Despite their importance, many fundamental aspects of chytrid developmental and cell biology remain poorly understood. To address these knowledge gaps, we combined quantitative volume electron microscopy and comparative transcriptome profiling to create an ‘atlas’ of the cellular and molecular basis of the chytrid life cycle, using the model chytrid Rhizoclosmatium globosum. From our developmental atlas, we describe the transition from the transcriptionally inactive free-swimming zoospore to the more biologically complex germling, and show that lipid processing is multifaceted and dynamic throughout the life cycle. We demonstrate that the chytrid apophysis is a compartmentalised site of high intracellular trafficking, linking the feeding/attaching rhizoids to the reproductive zoosporangium, and constituting division of labour in the chytrid cell plan. We provide evidence that during zoosporogenesis, zoospores display amoeboid morphologies and exhibit endocytotic cargo transport from the interstitial maternal cytoplasm. Taken together, our results reveal insights into chytrid developmental biology and provide a basis for future investigations into non-dikaryan fungal cell biology. |
format | Online Article Text |
id | pubmed-8887899 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-88878992022-03-02 A cellular and molecular atlas reveals the basis of chytrid development Laundon, Davis Chrismas, Nathan Bird, Kimberley Thomas, Seth Mock, Thomas Cunliffe, Michael eLife Cell Biology The chytrids (phylum Chytridiomycota) are a major fungal lineage of ecological and evolutionary importance. Despite their importance, many fundamental aspects of chytrid developmental and cell biology remain poorly understood. To address these knowledge gaps, we combined quantitative volume electron microscopy and comparative transcriptome profiling to create an ‘atlas’ of the cellular and molecular basis of the chytrid life cycle, using the model chytrid Rhizoclosmatium globosum. From our developmental atlas, we describe the transition from the transcriptionally inactive free-swimming zoospore to the more biologically complex germling, and show that lipid processing is multifaceted and dynamic throughout the life cycle. We demonstrate that the chytrid apophysis is a compartmentalised site of high intracellular trafficking, linking the feeding/attaching rhizoids to the reproductive zoosporangium, and constituting division of labour in the chytrid cell plan. We provide evidence that during zoosporogenesis, zoospores display amoeboid morphologies and exhibit endocytotic cargo transport from the interstitial maternal cytoplasm. Taken together, our results reveal insights into chytrid developmental biology and provide a basis for future investigations into non-dikaryan fungal cell biology. eLife Sciences Publications, Ltd 2022-03-01 /pmc/articles/PMC8887899/ /pubmed/35227375 http://dx.doi.org/10.7554/eLife.73933 Text en © 2022, Laundon 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 Laundon, Davis Chrismas, Nathan Bird, Kimberley Thomas, Seth Mock, Thomas Cunliffe, Michael A cellular and molecular atlas reveals the basis of chytrid development |
title | A cellular and molecular atlas reveals the basis of chytrid development |
title_full | A cellular and molecular atlas reveals the basis of chytrid development |
title_fullStr | A cellular and molecular atlas reveals the basis of chytrid development |
title_full_unstemmed | A cellular and molecular atlas reveals the basis of chytrid development |
title_short | A cellular and molecular atlas reveals the basis of chytrid development |
title_sort | cellular and molecular atlas reveals the basis of chytrid development |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8887899/ https://www.ncbi.nlm.nih.gov/pubmed/35227375 http://dx.doi.org/10.7554/eLife.73933 |
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