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Aurora A depletion reveals centrosome-independent polarization mechanism in Caenorhabditis elegans

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 PA...

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Autores principales: Klinkert, Kerstin, Levernier, Nicolas, Gross, Peter, Gentili, Christian, von Tobel, Lukas, Pierron, Marie, Busso, Coralie, Herrman, Sarah, Grill, Stephan W, Kruse, Karsten, Gönczy, Pierre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6417861/
https://www.ncbi.nlm.nih.gov/pubmed/30801250
http://dx.doi.org/10.7554/eLife.44552
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author Klinkert, Kerstin
Levernier, Nicolas
Gross, Peter
Gentili, Christian
von Tobel, Lukas
Pierron, Marie
Busso, Coralie
Herrman, Sarah
Grill, Stephan W
Kruse, Karsten
Gönczy, Pierre
author_facet Klinkert, Kerstin
Levernier, Nicolas
Gross, Peter
Gentili, Christian
von Tobel, Lukas
Pierron, Marie
Busso, Coralie
Herrman, Sarah
Grill, Stephan W
Kruse, Karsten
Gönczy, Pierre
author_sort Klinkert, Kerstin
collection PubMed
description 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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spelling pubmed-64178612019-03-15 Aurora A depletion reveals centrosome-independent polarization mechanism in Caenorhabditis elegans Klinkert, Kerstin Levernier, Nicolas Gross, Peter Gentili, Christian von Tobel, Lukas Pierron, Marie Busso, Coralie Herrman, Sarah Grill, Stephan W Kruse, Karsten Gönczy, Pierre eLife Cell Biology 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. eLife Sciences Publications, Ltd 2019-02-26 /pmc/articles/PMC6417861/ /pubmed/30801250 http://dx.doi.org/10.7554/eLife.44552 Text en © 2019, Klinkert et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Cell Biology
Klinkert, Kerstin
Levernier, Nicolas
Gross, Peter
Gentili, Christian
von Tobel, Lukas
Pierron, Marie
Busso, Coralie
Herrman, Sarah
Grill, Stephan W
Kruse, Karsten
Gönczy, Pierre
Aurora A depletion reveals centrosome-independent polarization mechanism in Caenorhabditis elegans
title Aurora A depletion reveals centrosome-independent polarization mechanism in Caenorhabditis elegans
title_full Aurora A depletion reveals centrosome-independent polarization mechanism in Caenorhabditis elegans
title_fullStr Aurora A depletion reveals centrosome-independent polarization mechanism in Caenorhabditis elegans
title_full_unstemmed Aurora A depletion reveals centrosome-independent polarization mechanism in Caenorhabditis elegans
title_short Aurora A depletion reveals centrosome-independent polarization mechanism in Caenorhabditis elegans
title_sort aurora a depletion reveals centrosome-independent polarization mechanism in caenorhabditis elegans
topic Cell Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6417861/
https://www.ncbi.nlm.nih.gov/pubmed/30801250
http://dx.doi.org/10.7554/eLife.44552
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