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Germ fate determinants protect germ precursor cell division by reducing septin and anillin levels at the cell division plane.
- Source :
-
Molecular biology of the cell [Mol Biol Cell] 2024 Jul 01; Vol. 35 (7), pp. ar94. Date of Electronic Publication: 2024 May 02. - Publication Year :
- 2024
-
Abstract
- 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 formin <superscript>cyk-1</superscript> (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 septin <superscript>UNC-59</superscript> and anillin <superscript>ANI-1</superscript> 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.
- Subjects :
- Animals
Contractile Proteins metabolism
Actomyosin metabolism
Cytokinesis physiology
Caenorhabditis elegans metabolism
Caenorhabditis elegans embryology
Caenorhabditis elegans Proteins metabolism
Caenorhabditis elegans Proteins genetics
Septins metabolism
Septins genetics
Cell Division
Germ Cells metabolism
Germ Cells cytology
Actins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1939-4586
- Volume :
- 35
- Issue :
- 7
- Database :
- MEDLINE
- Journal :
- Molecular biology of the cell
- Publication Type :
- Academic Journal
- Accession number :
- 38696255
- Full Text :
- https://doi.org/10.1091/mbc.E24-02-0096-T