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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2019
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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. |
format | Online Article Text |
id | pubmed-6417861 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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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