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Heimdallarchaea encodes profilin with eukaryotic-like actin regulation and polyproline binding
Stockholm University, Faculty of Science, Department of Molecular Biosciences, The Wenner-Gren Institute.
Stockholm University, Faculty of Science, Department of Molecular Biosciences, The Wenner-Gren Institute.
Stockholm University, Faculty of Science, Department of Molecular Biosciences, The Wenner-Gren Institute.
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Number of Authors: 82021 (English)In: Communications Biology, E-ISSN 2399-3642, Vol. 4, no 1, article id 1024Article in journal (Refereed) Published
Abstract [en]

It is now widely accepted that the first eukaryotic cell emerged from a merger of an archaeal host cell and an alphaproteobacterium. However, the exact sequence of events and the nature of the cellular biology of both partner cells is still contentious. Recently the structures of profilins from some members of the newly discovered Asgard superphylum were determined. In addition, it was found that these profilins inhibit eukaryotic rabbit actin polymerization and that this reaction is regulated by phospholipids. However, the interaction with polyproline repeats which are known to be crucial for the regulation of profilin:actin polymerization was found to be absent for these profilins and was thus suggested to have evolved later in the eukaryotic lineage. Here, we show that Heimdallarchaeota LC3, a candidate phylum within the Asgard superphylum, encodes a putative profilin (heimProfilin) that interacts with PIP2 and its binding is regulated by polyproline motifs, suggesting an origin predating the rise of the eukaryotes. More precisely, we determined the 3D-structure of Heimdallarchaeota LC3 profilin and show that this profilin is able to: i) inhibit eukaryotic actin polymerization in vitro; ii) bind to phospholipids; iii) bind to polyproline repeats from enabled/vasodilator‐stimulated phosphoprotein; iv) inhibit actin from Heimdallarchaeota from polymerizing into filaments. Our results therefore provide hints of the existence of a complex cytoskeleton already in last eukaryotic common ancestor.

Place, publisher, year, edition, pages
2021. Vol. 4, no 1, article id 1024
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Biological Sciences
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URN: urn:nbn:se:su:diva-197311DOI: 10.1038/s42003-021-02543-xISI: 000692407000005PubMedID: 34471213OAI: oai:DiVA.org:su-197311DiVA, id: diva2:1598766
Available from: 2021-09-29 Created: 2021-09-29 Last updated: 2022-02-25Bibliographically approved

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Survery, SabeenHurtig, FredrikHaq, Syed RazaulLindås, Ann-ChristinChi, Celestine N.

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Survery, SabeenHurtig, FredrikHaq, Syed RazaulLindås, Ann-ChristinChi, Celestine N.
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