Asymmetric distribution of actin-related proteins in the early C. elegans embryo

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The study investigated how actin-related proteins are differentially partitioned during early embryonic development in C. elegans, from the zygote to the 4-cell stage, focusing on actin polymerization regulators including a formin, the Arp2/3 complex, a capping protein, and E-cadherin. Using thorough intracellular distribution quantification alongside a new method to assess actin polymerization capacities from single blastomere extracts, the authors found that actin-related signatures emerge early and that protein segregation and homeostasis depend on both the specific cell pair and the protein considered. They also observed that after asymmetric divisions, AB daughter cells show differences linked to embryonic polarity, indicating unequal partitioning of actin-related contents. The paper is not explicit about limitations in the excerpt provided, but it remains centered on early C. elegans embryogenesis rather than disease biology. The paper does not explicitly discuss endometriosis or adenomyosis; it was included in the corpus via a keyword match in the upstream search index.

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Abstract To achieve a stereotypic lineage, each embryo of Caenorhabditis elegans follows an invariant cell differentiation process arising from a combination of cell polarisation, asymmetric or symmetric divisions, combined with intercellular signalling processes. This pattern of embryonic cell differentiation is driven by regulated segregation of molecules occurring at each cell division, including polarity proteins or cell fate determinants, transcription factors, p-granules and mRNAs. These distribution patterns are coupled with a robust spatio-temporal orchestration of cortical actin dynamics, which also plays a crucial role in these processes. However, compared to other molecular contents, how the actin per se is segregated from the first asymmetric division onward remains poorly understood. This study presents a thorough quantification of the intracellular distribution from the zygote to the 4-cell stage of key actors related to actin polymerisation: two nucleators (a formin and the Arp2/3 complex), a capping protein and E-cadherin. We additionally developed a novel method to assess actin polymerisation capacities from single blastomere extracts. We found that actin-related signatures arise at these early stages and that differential mechanisms of protein segregation and homeostasis occur, depending both on the cell pair and on the protein considered. Notably, if asymmetric divisions correlated with unequal partitioning of actin-related contents in a process linked with embryonic polarity, differences were revealed between AB daughter cells upon their separation. Taken together, these actin-related asymmetric distributions are adding a layer to the complexity of cell fate acquisition mechanisms in the early embryo. Competing Interest Statement The authors have declared no competing interest. Footnotes Université de Strasbourg, CNRS, Inserm, IGBMC UMR 7104- UMR-S 1258, F-67400 Illkirch, France Typo correction in one of the author's name

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