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Chytrid rhizoid morphogenesis resembles hyphal development in multicellular fungi and is adaptive to resource availability

Key to the ecological prominence of fungi is their distinctive cell biology, our understanding of which has been principally based on dikaryan hyphal and yeast forms. The early-diverging Chytridiomycota (chytrids) are ecologically important and a significant component of fungal diversity, yet their...

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Autores principales: Laundon, Davis, Chrismas, Nathan, Wheeler, Glen, Cunliffe, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7341943/
https://www.ncbi.nlm.nih.gov/pubmed/32517626
http://dx.doi.org/10.1098/rspb.2020.0433
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author Laundon, Davis
Chrismas, Nathan
Wheeler, Glen
Cunliffe, Michael
author_facet Laundon, Davis
Chrismas, Nathan
Wheeler, Glen
Cunliffe, Michael
author_sort Laundon, Davis
collection PubMed
description Key to the ecological prominence of fungi is their distinctive cell biology, our understanding of which has been principally based on dikaryan hyphal and yeast forms. The early-diverging Chytridiomycota (chytrids) are ecologically important and a significant component of fungal diversity, yet their cell biology remains poorly understood. Unlike dikaryan hyphae, chytrids typically attach to substrates and feed osmotrophically via anucleate rhizoids. The evolution of fungal hyphae appears to have occurred from rhizoid-bearing lineages and it has been hypothesized that a rhizoid-like structure was the precursor to multicellular hyphae. Here, we show in a unicellular chytrid, Rhizoclosmatium globosum, that rhizoid development exhibits striking similarities with dikaryan hyphae and is adaptive to resource availability. Rhizoid morphogenesis exhibits analogous patterns to hyphal growth and is controlled by β-glucan-dependent cell wall synthesis and actin polymerization. Chytrid rhizoids growing from individual cells also demonstrate adaptive morphological plasticity in response to resource availability, developing a searching phenotype when carbon starved and spatial differentiation when interacting with particulate organic matter. We demonstrate that the adaptive cell biology and associated developmental plasticity considered characteristic of hyphal fungi are shared more widely across the Kingdom Fungi and therefore could be conserved from their most recent common ancestor.
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spelling pubmed-73419432020-07-12 Chytrid rhizoid morphogenesis resembles hyphal development in multicellular fungi and is adaptive to resource availability Laundon, Davis Chrismas, Nathan Wheeler, Glen Cunliffe, Michael Proc Biol Sci Development and Physiology Key to the ecological prominence of fungi is their distinctive cell biology, our understanding of which has been principally based on dikaryan hyphal and yeast forms. The early-diverging Chytridiomycota (chytrids) are ecologically important and a significant component of fungal diversity, yet their cell biology remains poorly understood. Unlike dikaryan hyphae, chytrids typically attach to substrates and feed osmotrophically via anucleate rhizoids. The evolution of fungal hyphae appears to have occurred from rhizoid-bearing lineages and it has been hypothesized that a rhizoid-like structure was the precursor to multicellular hyphae. Here, we show in a unicellular chytrid, Rhizoclosmatium globosum, that rhizoid development exhibits striking similarities with dikaryan hyphae and is adaptive to resource availability. Rhizoid morphogenesis exhibits analogous patterns to hyphal growth and is controlled by β-glucan-dependent cell wall synthesis and actin polymerization. Chytrid rhizoids growing from individual cells also demonstrate adaptive morphological plasticity in response to resource availability, developing a searching phenotype when carbon starved and spatial differentiation when interacting with particulate organic matter. We demonstrate that the adaptive cell biology and associated developmental plasticity considered characteristic of hyphal fungi are shared more widely across the Kingdom Fungi and therefore could be conserved from their most recent common ancestor. The Royal Society 2020-06-10 2020-06-10 /pmc/articles/PMC7341943/ /pubmed/32517626 http://dx.doi.org/10.1098/rspb.2020.0433 Text en © 2020 The Authors. http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/http://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Development and Physiology
Laundon, Davis
Chrismas, Nathan
Wheeler, Glen
Cunliffe, Michael
Chytrid rhizoid morphogenesis resembles hyphal development in multicellular fungi and is adaptive to resource availability
title Chytrid rhizoid morphogenesis resembles hyphal development in multicellular fungi and is adaptive to resource availability
title_full Chytrid rhizoid morphogenesis resembles hyphal development in multicellular fungi and is adaptive to resource availability
title_fullStr Chytrid rhizoid morphogenesis resembles hyphal development in multicellular fungi and is adaptive to resource availability
title_full_unstemmed Chytrid rhizoid morphogenesis resembles hyphal development in multicellular fungi and is adaptive to resource availability
title_short Chytrid rhizoid morphogenesis resembles hyphal development in multicellular fungi and is adaptive to resource availability
title_sort chytrid rhizoid morphogenesis resembles hyphal development in multicellular fungi and is adaptive to resource availability
topic Development and Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7341943/
https://www.ncbi.nlm.nih.gov/pubmed/32517626
http://dx.doi.org/10.1098/rspb.2020.0433
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