4.8 Article

Contact area-dependent cell communication and the morphological invariance of ascidian embryogenesis

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SCIENCE
卷 369, 期 6500, 页码 158-+

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AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.aar5663

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资金

  1. CNRS
  2. Inria
  3. Geneshape project [ANR-SYSC-018-02]
  4. Dig-Em project [ANR-14-CE11-0013-01]
  5. European Molecular Biology Laboratory of the University of Heidelberg
  6. Center of Modeling and Simulation in the Biosciences (BIOMS) of the University of Heidelberg
  7. CBS2 doctoral school of the University of Montpellier 2
  8. Fondation pour la Recherche Medicale (FRM) [FDT20140931061]
  9. Morphoscope2 Equipex project [ANR-11-EQPX-0029]
  10. Geneshape Project
  11. Dig-Em project
  12. FRM [SPF20120523969]
  13. EMBL Interdisciplinary Postdoc Programme under Marie Curie Actions
  14. Institut de Biologie Computationnelle of Montpellier (IBC) [ANR-11-BINF-0002]
  15. Inria (IPL Morphogenetics)
  16. EpiGenMed laboratory of excellence [ANR-10-LABX-12-01]
  17. Fondation Bettencourt-Schueller

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Marine invertebrate ascidians display embryonic reproducibility: Their early embryonic cell lineages are considered invariant and are conserved between distantly related species, despite rapid genomic divergence. Here, we address the drivers of this reproducibility. We used light-sheet imaging and automated cell segmentation and tracking procedures to systematically quantify the behavior of individual cells every 2 minutes during Phallusia mammillata embryogenesis. Interindividual reproducibility was observed down to the area of individual cell contacts. We found tight links between the reproducibility of embryonic geometries and asymmetric cell divisions, controlled by differential sister cell inductions. We combined modeling and experimental manipulations to show that the area of contact between signaling and responding cells is a key determinant of cell communication. Our work establishes the geometric control of embryonic inductions as an alternative to classical morphogen gradients and suggests that the range of cell signaling sets the scale at which embryonic reproducibility is observed.

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