4.5 Article

The Ancestral Mitotic State: Closed Orthomitosis With Intranuclear Spindles in the Syncytial Last Eukaryotic Common Ancestor

Journal

GENOME BIOLOGY AND EVOLUTION
Volume 15, Issue 3, Pages -

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/gbe/evad016

Keywords

last eukaryotic common ancestor; ancestral state reconstruction; mitosis; syncytium; eukaryogenesis

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All eukaryotes have linear chromosomes distributed during mitotic division. However, the ancestral state of nuclear division in the last eukaryotic common ancestor (LECA) remains unknown. Ancestral state reconstructions suggest that LECA had closed orthomitosis with intranuclear spindles. This finding contributes to our understanding of LECA's lifestyle and adds to the list of cellular traits attributed to this enigmatic biological entity.
All eukaryotes have linear chromosomes that are distributed to daughter nuclei during mitotic division, but the ancestral state of nuclear division in the last eukaryotic common ancestor (LECA) is so far unresolved. To address this issue, we have employed ancestral state reconstructions for mitotic states that can be found across the eukaryotic tree concerning the intactness of the nuclear envelope during mitosis (open or closed), the position of spindles (intranuclear or extranuclear), and the symmetry of spindles being either axial (orthomitosis) or bilateral (pleuromitosis). The data indicate that the LECA possessed closed orthomitosis with intranuclear spindles. Our reconstruction is compatible with recent findings indicating a syncytial state of the LECA, because it decouples three main processes: chromosome division, chromosome partitioning, and cell division (cytokinesis). The possession of closed mitosis using intranuclear spindles adds to the number of cellular traits that can now be attributed to LECA, providing insights into the lifestyle of this otherwise elusive biological entity at the origin of eukaryotic cells. Closed mitosis in a syncytial eukaryotic common ancestor would buffer mutations arising at the origin of mitotic division by allowing nuclei with viable chromosome sets to complement defective nuclei via mRNA in the cytosol.

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