Aurora a depletion reveals centrosome-independent polarization mechanism in caenorhabditis elegans

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Kerstin Klinkert - (Author)
  • Nicolas Levernier - (Author)
  • Peter Gross - , Chair of Biophysics (Author)
  • Christian Gentili - (Author)
  • Lukas Von Tobel - (Author)
  • Marie Pierron - (Author)
  • Coralie Busso - (Author)
  • Sarah Herrman - (Author)
  • Stephan W. Grill - , Chair of Biophysics, Clusters of Excellence PoL: Physics of Life, Max Planck Institute of Molecular Cell Biology and Genetics (Author)
  • Karsten Kruse - (Author)
  • Pierre Gönczy - (Author)

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.

Details

Original languageEnglish
Article numbere44552
JournaleLife
Volume8
Publication statusPublished - Feb 2019
Peer-reviewedYes

External IDs

PubMed 30801250