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 PMID:38696255  

Germ fate determinants protect germ precursor cell division by reducing septin and anillin levels at the cell division plane.

Caroline Q Connors | Michael S Mauro | J Tristian Wiles | Andrew D Countryman | Sophia L Martin | Benjamin Lacroix | Mimi Shirasu-Hiza | Julien Dumont | Karen E Kasza | Timothy R Davies | Julie C Canman
Molecular biology of the cell | 2024

Animal cell cytokinesis, or the physical division of one cell into two, is thought to be driven by constriction of an actomyosin contractile ring at the division plane. The mechanisms underlying cell type-specific differences in cytokinesis remain unknown. Germ cells are totipotent cells that pass genetic information to the next generation. Previously, using formincyk-1(ts) mutant Caenorhabditis elegans 4-cell embryos, we found that the P2 germ precursor cell is protected from cytokinesis failure and can divide with greatly reduced F-actin levels at the cell division plane. Here, we identified two canonical germ fate determinants required for P2-specific cytokinetic protection: PIE-1 and POS-1. Neither has been implicated previously in cytokinesis. These germ fate determinants protect P2 cytokinesis by reducing the accumulation of septinUNC-59 and anillinANI-1 at the division plane, which here act as negative regulators of cytokinesis. These findings may provide insight into the regulation of cytokinesis in other cell types, especially in stem cells with high potency.

Pubmed ID: 38696255

Antibodies used in this publication

None found

Associated grants

  • Agency: NIGMS NIH HHS, United States
    Id: R01 GM117407
  • Agency: NIH HHS, United States
    Id: P40 OD010440
  • Agency: NIA NIH HHS, United States
    Id: R01 AG045842
  • Agency: NIGMS NIH HHS, United States
    Id: R35 GM138380
  • Agency: NIGMS NIH HHS, United States
    Id: R35 GM127049

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RRID:SCR_007341

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