Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Extraembryonic proteases regulate Nodal signalling during gastrulation.

Séverine Beck1, J Ann Le Good, Marcela Guzman

  • 1Developmental Biology Group, Swiss Institute for Experimental Cancer Research (ISREC), Chemin des Boveresses 155, CH-1066 Epalinges, Switzerland.

Nature Cell Biology
|November 26, 2002
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

FluoTag-EMSA: a fast and accessible quantitative method to assess RNA-binding specificity using 3'-tagged hybrid duplexes.

Frontiers in molecular biosciences·2025
Same author

m<sup>6</sup>A methylation inhibits recruitment of the <i>Dand5</i> 3'UTR to the left-right determinant Bicc1.

RNA (New York, N.Y.)·2025
Same author

Kallikrein-8 mediates furin-independent Activin-A precursor processing to stimulate tumor growth in melanoma.

Nature communications·2025
Same author

Stepwise release of Activin-A from its inhibitory prodomain is modulated by cysteines and requires furin coexpression to promote melanoma growth.

Communications biology·2024
Same author

Inhibition of anti-tumor immunity by melanoma cell-derived Activin-A depends on STING.

Frontiers in immunology·2024
Same author

Bicc1 ribonucleoprotein complexes specifying organ laterality are licensed by ANKS6-induced structural remodeling of associated ANKS3.

PLoS biology·2023

Proprotein convertases Spc1 and Spc4 are essential for Nodal signaling during mammalian embryonic development. These enzymes mature Nodal protein, enabling antero-posterior pattern formation and Cripto induction.

Area of Science:

  • Developmental Biology
  • Molecular Biology
  • Genetics

Background:

  • Embryonic development relies on precise inductive signaling pathways.
  • Nodal signaling is crucial for establishing antero-posterior polarity during gastrulation.
  • Cripto acts as a co-receptor downstream of Nodal, mediating its effects.

Purpose of the Study:

  • To investigate the role of proprotein convertases Spc1 and Spc4 in Nodal signaling.
  • To determine the mechanism by which Nodal induces Cripto expression.
  • To elucidate the contribution of Spc1 and Spc4 to embryonic patterning.

Main Methods:

  • Analysis of Spc1 and Spc4 expression in extraembryonic ectoderm.
  • In vivo studies using Spc1(-/-); Spc4(-/-) double mutant mice.

Related Experiment Videos

  • Embryo explant experiments with and without extraembryonic ectoderm.
  • Functional rescue experiments using recombinant mature Nodal.
  • Main Results:

    • Spc1 and Spc4 are expressed in extraembryonic ectoderm and are required for Nodal signaling.
    • These proteases stimulate Nodal maturation and are essential for Cripto induction.
    • Lack of Spc1/Spc4 impairs Nodal-mediated Cripto induction and also affects Bone Morphogenetic Protein 4 (BMP4) induction.

    Conclusions:

    • Spc1 and Spc4 are critical for Nodal maturation and subsequent signaling during mammalian gastrulation.
    • Nodal induces Cripto through both direct embryonic signaling and indirect induction of BMP4 in extraembryonic tissues.
    • Spc1 and Spc4 regulate both Nodal maturation and BMP4 induction, highlighting their central role in embryonic patterning.