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

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.

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Klinkert, Kerstin, Author
Levernier, Nicolas, Author
Gross, Peter1, Author           
Gentili, Christian, Author
Tobel, Lukas von, Author
Pierron, Marie, Author
Busso, Coralie, Author
Herrman, Sarah, Author
Grill, Stephan W.1, Author           
Kruse, Karsten, Author
Gönczy, Pierre, Author
Affiliations:
1Max Planck Institute for Molecular Cell Biology and Genetics, Max Planck Society, ou_2340692              

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 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.

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 Dates: 2019-02-25
 Publication Status: Issued
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 Identifiers: DOI: 10.7554/eLife.44552
Other: cbg-7351
PMID: 30801250
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Title: eLife
  Other : Elife
Source Genre: Journal
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Pages: - Volume / Issue: 8 Sequence Number: e44552 Start / End Page: - Identifier: -