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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...

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Autores principales: Laundon, Davis, Chrismas, Nathan, Bird, Kimberley, Thomas, Seth, Mock, Thomas, Cunliffe, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2022
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.
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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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