Evidence map›Paper›PMID 42777007›Full record

ArticlePLoS computational biology2026

Nematic structures contribute to robust zygotic polarization in C. elegans.

Michiel Vanslambrouck, Jef Vangheel, Ella Linxia Müller, Bart Smeets, Pierre Gönczy, Rob Jelier

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In one paragraph

Article in PLoS computational biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Michiel VanslambrouckCMPG, M2S Department, KU Leuven, Heverlee, Belgium.
Jef VangheelMeBioS, Department of Biosystems, KU Leuven, Heverlee, Belgium.
Ella Linxia MüllerISREC, School of Life Sciences, EPFL, Lausanne, Switzerland.
Bart SmeetsMeBioS, Department of Biosystems, KU Leuven, Heverlee, Belgium.
Pierre GönczyISREC, School of Life Sciences, EPFL, Lausanne, Switzerland.
Rob JelierCMPG, M2S Department, KU Leuven, Heverlee, Belgium.ORCID https://orcid.org/0000-0002-6395-1407

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The C. elegans zygote is a powerful model for asymmetric cell division. Its strikingly patterned cortex features thick F-actin bundles and myosin foci, contractile nematic structures that drive characteristic surface ruffles. Approximately 30 min after fertilization, symmetry breaks near the sperm-contributed centrosomes, typically at the presumptive posterior pole, and is marked by local downregulation of contractility. This initiates a cortical flow that polarizes the cell and enables PAR proteins to establish anterior and posterior domains. While biochemical mechanisms maintaining these domains are well understood, the mechanical role of cortical architecture in polarization remains unclear. We developed a three-dimensional (3D) mechanical model of C. elegans zygote polarization that represents the actin bundles and myosin foci of the cortex as a network of stiff contractile filaments. We measured cortical flow with high spatiotemporal resolution by tracking myosin foci, and used these data alongside mechanical properties from the literature to parametrize the model. The model simulates the complete polarization process in 3D, from symmetry breaking through domain stabilization, and reproduces key cortical dynamics including flow profiles, surface ruffles, and tension anisotropy. Domain arrest near the embryo midpoint emerges from density-dependent contractility regulation, in which cortical material redistribution during flow creates a mechanical negative feedback that balances anterior and posterior tension. We find that compressive flow aligns actin bundles in the anterior domain and generates anisotropic tension perpendicular to the flow direction. Although this alignment is not essential for polarization when symmetry breaking occurs at the pole, it contributes to this process when symmetry breaking occurs laterally. In such cases, anisotropic tension from aligned bundles drives axis convergence by rotating the posterior domain towards the nearest pole. Nematic cortical structures therefore ensure robust alignment of the polarization axis.

Indexed as

Caenorhabditis elegansCell PolarityModels, BiologicalZygoteActin CytoskeletonActinsAnimalsCaenorhabditis elegans ProteinsMyosinsActinsCaenorhabditis elegans ProteinsMyosins

Identifiers

PMID42777007
PMCPMC13630317

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.