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Multiple Roots of Fruiting Body Formation in Amoebozoa

Establishment of multicellularity represents a major transition in eukaryote evolution. A subgroup of Amoebozoa, the dictyosteliids, has evolved a relatively simple aggregative multicellular stage resulting in a fruiting body supported by a stalk. Protosteloid amoeba, which are scattered throughout...

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Autores principales: Hillmann, Falk, Forbes, Gillian, Novohradská, Silvia, Ferling, Iuliia, Riege, Konstantin, Groth, Marco, Westermann, Martin, Marz, Manja, Spaller, Thomas, Winckler, Thomas, Schaap, Pauline, Glöckner, Gernot
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5804921/
https://www.ncbi.nlm.nih.gov/pubmed/29378020
http://dx.doi.org/10.1093/gbe/evy011
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author Hillmann, Falk
Forbes, Gillian
Novohradská, Silvia
Ferling, Iuliia
Riege, Konstantin
Groth, Marco
Westermann, Martin
Marz, Manja
Spaller, Thomas
Winckler, Thomas
Schaap, Pauline
Glöckner, Gernot
author_facet Hillmann, Falk
Forbes, Gillian
Novohradská, Silvia
Ferling, Iuliia
Riege, Konstantin
Groth, Marco
Westermann, Martin
Marz, Manja
Spaller, Thomas
Winckler, Thomas
Schaap, Pauline
Glöckner, Gernot
author_sort Hillmann, Falk
collection PubMed
description Establishment of multicellularity represents a major transition in eukaryote evolution. A subgroup of Amoebozoa, the dictyosteliids, has evolved a relatively simple aggregative multicellular stage resulting in a fruiting body supported by a stalk. Protosteloid amoeba, which are scattered throughout the amoebozoan tree, differ by producing only one or few single stalked spores. Thus, one obvious difference in the developmental cycle of protosteliids and dictyosteliids seems to be the establishment of multicellularity. To separate spore development from multicellular interactions, we compared the genome and transcriptome of a Protostelium species (Protostelium aurantium var. fungivorum) with those of social and solitary members of the Amoebozoa. During fruiting body formation nearly 4,000 genes, corresponding to specific pathways required for differentiation processes, are upregulated. A comparison with genes involved in the development of dictyosteliids revealed conservation of >500 genes, but most of them are also present in Acanthamoeba castellanii for which fruiting bodies have not been documented. Moreover, expression regulation of those genes differs between P. aurantium and Dictyostelium discoideum. Within Amoebozoa differentiation to fruiting bodies is common, but our current genome analysis suggests that protosteliids and dictyosteliids used different routes to achieve this. Most remarkable is both the large repertoire and diversity between species in genes that mediate environmental sensing and signal processing. This likely reflects an immense adaptability of the single cell stage to varying environmental conditions. We surmise that this signaling repertoire provided sufficient building blocks to accommodate the relatively simple demands for cell–cell communication in the early multicellular forms.
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spelling pubmed-58049212018-02-23 Multiple Roots of Fruiting Body Formation in Amoebozoa Hillmann, Falk Forbes, Gillian Novohradská, Silvia Ferling, Iuliia Riege, Konstantin Groth, Marco Westermann, Martin Marz, Manja Spaller, Thomas Winckler, Thomas Schaap, Pauline Glöckner, Gernot Genome Biol Evol Research Article Establishment of multicellularity represents a major transition in eukaryote evolution. A subgroup of Amoebozoa, the dictyosteliids, has evolved a relatively simple aggregative multicellular stage resulting in a fruiting body supported by a stalk. Protosteloid amoeba, which are scattered throughout the amoebozoan tree, differ by producing only one or few single stalked spores. Thus, one obvious difference in the developmental cycle of protosteliids and dictyosteliids seems to be the establishment of multicellularity. To separate spore development from multicellular interactions, we compared the genome and transcriptome of a Protostelium species (Protostelium aurantium var. fungivorum) with those of social and solitary members of the Amoebozoa. During fruiting body formation nearly 4,000 genes, corresponding to specific pathways required for differentiation processes, are upregulated. A comparison with genes involved in the development of dictyosteliids revealed conservation of >500 genes, but most of them are also present in Acanthamoeba castellanii for which fruiting bodies have not been documented. Moreover, expression regulation of those genes differs between P. aurantium and Dictyostelium discoideum. Within Amoebozoa differentiation to fruiting bodies is common, but our current genome analysis suggests that protosteliids and dictyosteliids used different routes to achieve this. Most remarkable is both the large repertoire and diversity between species in genes that mediate environmental sensing and signal processing. This likely reflects an immense adaptability of the single cell stage to varying environmental conditions. We surmise that this signaling repertoire provided sufficient building blocks to accommodate the relatively simple demands for cell–cell communication in the early multicellular forms. Oxford University Press 2018-01-25 /pmc/articles/PMC5804921/ /pubmed/29378020 http://dx.doi.org/10.1093/gbe/evy011 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Research Article
Hillmann, Falk
Forbes, Gillian
Novohradská, Silvia
Ferling, Iuliia
Riege, Konstantin
Groth, Marco
Westermann, Martin
Marz, Manja
Spaller, Thomas
Winckler, Thomas
Schaap, Pauline
Glöckner, Gernot
Multiple Roots of Fruiting Body Formation in Amoebozoa
title Multiple Roots of Fruiting Body Formation in Amoebozoa
title_full Multiple Roots of Fruiting Body Formation in Amoebozoa
title_fullStr Multiple Roots of Fruiting Body Formation in Amoebozoa
title_full_unstemmed Multiple Roots of Fruiting Body Formation in Amoebozoa
title_short Multiple Roots of Fruiting Body Formation in Amoebozoa
title_sort multiple roots of fruiting body formation in amoebozoa
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5804921/
https://www.ncbi.nlm.nih.gov/pubmed/29378020
http://dx.doi.org/10.1093/gbe/evy011
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