Evidence map›Paper›PMID 29378020›Full record

ArticleGenome biology and evolution2018

Multiple Roots of Fruiting Body Formation in Amoebozoa.

Falk Hillmann, Gillian Forbes, Silvia Novohradská, Iuliia Ferling, Konstantin Riege, Marco Groth, Martin Westermann, Manja Marz, Thomas Spaller, Thomas Winckler and 2 more

Abstract read
In one paragraph

Article in Genome biology and evolution, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

18 citing papers in PubMed.

  1. Article
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  9. Review
  10. Review
  11. Article
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  14. Article
  15. A well supported multi gene phylogeny of 52 dictyostelia.Molecular phylogenetics and evolution · 2019
    Article
  16. Evolution of multicellularity in Dictyostelia.The International journal of developmental biology · 2019
    Review
  17. Article
  18. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Falk HillmannJunior Research Group Evolution of Microbial Interaction, Leibniz Institute for Natural Product Research and Infection Biology - Hans Knöll Institute (HKI), Jena, Germany.
Gillian ForbesDivision of Cell and Developmental Biology, School of Life Sciences, University of Dundee, United Kingdom.
Silvia NovohradskáJunior Research Group Evolution of Microbial Interaction, Leibniz Institute for Natural Product Research and Infection Biology - Hans Knöll Institute (HKI), Jena, Germany.
Iuliia FerlingJunior Research Group Evolution of Microbial Interaction, Leibniz Institute for Natural Product Research and Infection Biology - Hans Knöll Institute (HKI), Jena, Germany.
Konstantin RiegeBioinformatics/High Throughput Analysis, Friedrich Schiller University Jena, Germany.
Marco GrothCF DNA-Sequencing, Leibniz Institute on Aging Research, Jena, Germany.
Martin WestermannElectron Microscopy Center, Jena University Hospital, Germany.
Manja MarzBioinformatics/High Throughput Analysis, Friedrich Schiller University Jena, Germany.
Thomas SpallerPharmaceutical Biology, Institute of Pharmacy, Friedrich Schiller University Jena, Germany.
Thomas WincklerPharmaceutical Biology, Institute of Pharmacy, Friedrich Schiller University Jena, Germany.
Pauline SchaapDivision of Cell and Developmental Biology, School of Life Sciences, University of Dundee, United Kingdom.
Gernot GlöcknerInstitute of Biochemistry I, Medical Faculty, University of Cologne, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

Gene Expression Regulation, DevelopmentalAmoebozoaCell CommunicationDictyosteliumEvolution, MolecularPhylogenyProtozoan ProteinsTranscriptomeProtozoan ProteinsAmoebozoaDictyosteliaevolution of developmentmulticellular developmentProtosteliumsignalingtranscriptome

Identifiers

PMID29378020
PMCPMC5804921

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.