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Aurora A depletion reveals centrosome-independent polarization mechanism in C. elegans.

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Gross,  Peter
Max Planck Institute for Molecular Cell Biology and Genetics, Max Planck Society;

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Grill,  Stephan W.
Max Planck Institute for Molecular Cell Biology and Genetics, Max Planck Society;

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Citation

Klinkert, K., Levernier, N., Gross, P., Gentili, C., Tobel, L. v., Pierron, M., et al. (2019). Aurora A depletion reveals centrosome-independent polarization mechanism in C. elegans. eLife, 8: e44552. doi:10.7554/eLife.44552.


Cite as: https://hdl.handle.net/21.11116/0000-0006-7D3E-A
Abstract
How living systems break symmetry in an organized manner is a fundamental question in biology. In wild type Caenorhabditis elegans zygotes, symmetry breaking during anterior-posterior axis specification is guided by centrosomes, resulting in anterior-directed cortical flows and a single posterior PAR-2 domain. We uncover that C. elegans zygotes depleted of the Aurora A kinase AIR-1 or lacking centrosomes entirely usually establish two posterior PAR-2 domains, one at each pole. We demonstrate that AIR-1 prevents symmetry breaking early in the cell cycle, whereas centrosomal AIR-1 instructs polarity initiation thereafter. Using triangular microfabricated chambers, we establish that bipolarity of air-1(RNAi) embryos occurs effectively in a cell-shape and curvature-dependent manner. Furthermore, we develop an integrated physical description of symmetry breaking, wherein local PAR-2-dependent weakening of the actin cortex, together with mutual inhibition of anterior and posterior PAR proteins, provides a mechanism for spontaneous symmetry breaking without centrosomes.