Deciphering and modelling the TGF-β signalling interplays specifying the dorsal-ventral axis of the sea urchin embryo

Author:

Floc'hlay Swann1,Molina Maria Dolores2,Hernandez Céline1ORCID,Haillot Emmanuel2ORCID,Thomas-Chollier Morgane13ORCID,Lepage Thierry2ORCID,Thieffry Denis1ORCID

Affiliation:

1. Institut de Biologie de l'ENS (IBENS), École Normale Supérieure, CNRS, INSERM, Université PSL, 75005 Paris, France

2. Institut Biologie Valrose, Université Côte d'Azur, Nice, France

3. Institut Universitaire de France (IUF), 75005 Paris, France

Abstract

During sea urchin development, secretion of Nodal and BMP2/4 ligands and their antagonists Lefty and Chordin from a ventral organizer region specifies the ventral and dorsal territories. This process relies on a complex interplay between the Nodal and BMP pathways through numerous regulatory circuits. To decipher the interplay between these pathways, we used a combination of treatments with recombinant Nodal and BMP2/4 proteins and a computational modelling approach. We assembled a logical model focusing on cell responses to signalling inputs along the dorsal-ventral axis, which was extended to cover ligand diffusion and enable multicellular simulations. Our model simulations accurately recapitulate gene expression in wild type embryos, accounting for the specification of ventral ectoderm, ciliary band and dorsal ectoderm. Our model simulations further recapitulate various morphant phenotypes, reveals a dominance of the BMP pathway over the Nodal pathway, and stresses the crucial impact of the rate of Smad activation in D/V patterning. These results emphasise the key role of the mutual antagonism between the Nodal and BMP2/4 pathways in driving early dorsal-ventral patterning of the sea urchin embryo.

Funder

Agence Nationale de la Recherche

Fondation pour la Recherche Médicale

Association pour la Recherche sur le Cancer

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

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