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Aggregative multicellularity evolved independently in the eukaryotic supergroup Rhizaria
Matthew W Brown1, Martin Kolisko, Jeffrey D Silberman
1Centre for Comparative Genomics and Evolutionary Bioinformatics, Department of Biochemistry and Molecular Biology, Dalhousie University, Halifax, Nova Scotia, B3H 4R2, Canada. protist@live.com
Aggregative multicellularity, common in eukaryotes, was newly discovered in the Rhizaria supergroup. The species Guttulinopsis vulgaris exhibits this complex social behavior, expanding our understanding of life
Area of Science:
- Eukaryotic evolution
- Protistan biology
- Developmental biology
Background:
- Multicellularity has evolved independently multiple times in eukaryotes, leading to diverse lineages like animals, plants, and fungi.
- A common form of eukaryotic multicellularity involves social aggregative fruiting, forming sorocarps, famously studied in Dictyostelium discoideum.
- Sorocarpic protists have been identified across five major eukaryote groups, but Guttulinopsis vulgaris remained unclassified.
Purpose of the Study:
- To classify the globally distributed species Guttulinopsis vulgaris.
- To investigate the evolutionary origins of aggregative multicellularity in protists.
- To determine if Guttulinopsis vulgaris exhibits social aggregative fruiting behavior.
Main Methods:
- Phylogenomic analyses were conducted using a dataset comprising 159 proteins.
- The evolutionary placement of Guttulinopsis vulgaris within the eukaryotic tree of life was determined.
Main Results:
- Phylogenomic analyses placed Guttulinopsis vulgaris within the Rhizaria supergroup.
- This finding represents the first known instance of aggregative multicellularity in the Rhizaria.
- Guttulinopsis vulgaris demonstrates a complex, coordinated developmental process involving thousands of cells.
Conclusions:
- Guttulinopsis vulgaris is a member of the Rhizaria supergroup.
- The discovery of aggregative multicellularity in Rhizaria expands the known diversity of this complex trait.
- This finding highlights the independent evolution of multicellularity across major eukaryotic lineages.
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