Your browser doesn't support javascript.
loading
Deciphering and modelling the TGF-ß signalling interplays specifying the dorsal-ventral axis of the sea urchin embryo.
Floc'hlay, Swann; Molina, Maria Dolores; Hernandez, Céline; Haillot, Emmanuel; Thomas-Chollier, Morgane; Lepage, Thierry; Thieffry, Denis.
Afiliación
  • Floc'hlay S; Department of Biology, Institut de Biologie de l'ENS (IBENS), École Normale Supérieure, CNRS, INSERM, Université PSL, 75005 Paris, France.
  • Molina MD; Institut Biologie Valrose, Université Côte d'Azur, 06108 Nice, France.
  • Hernandez C; Department of Biology, Institut de Biologie de l'ENS (IBENS), École Normale Supérieure, CNRS, INSERM, Université PSL, 75005 Paris, France.
  • Haillot E; Institut Biologie Valrose, Université Côte d'Azur, 06108 Nice, France.
  • Thomas-Chollier M; Department of Biology, Institut de Biologie de l'ENS (IBENS), École Normale Supérieure, CNRS, INSERM, Université PSL, 75005 Paris, France.
  • Lepage T; Institut Universitaire de France (IUF), 75005 Paris, France.
  • Thieffry D; Institut Biologie Valrose, Université Côte d'Azur, 06108 Nice, France denis.thieffry@ens.psl.eu tlepage@unice.fr.
Development ; 148(2)2021 01 20.
Article en En | MEDLINE | ID: mdl-33298464
During sea urchin development, secretion of Nodal and BMP2/4 ligands and their antagonists Lefty and Chordin from a ventral organiser 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, reveal a dominance of the BMP pathway over the Nodal pathway and stress the crucial impact of the rate of Smad activation in dorsal-ventral 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.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Transducción de Señal / Factor de Crecimiento Transformador beta / Tipificación del Cuerpo / Paracentrotus / Embrión no Mamífero Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Development Asunto de la revista: BIOLOGIA / EMBRIOLOGIA Año: 2021 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Transducción de Señal / Factor de Crecimiento Transformador beta / Tipificación del Cuerpo / Paracentrotus / Embrión no Mamífero Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Development Asunto de la revista: BIOLOGIA / EMBRIOLOGIA Año: 2021 Tipo del documento: Article País de afiliación: Francia