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Eomesodermin is required for mouse trophoblast development and mesoderm formation

Author

Listed:
  • Andreas P. Russ

    (Wellcome/CRC Institute for Cancer and Developmental Biology, University of Cambridge
    University of Cambridge
    Paradigm Therapeutics Ltd)

  • Sigrid Wattler

    (Niedersächsisches Institut für Peptidforschung
    Ingenium Pharmaceuticals AG)

  • William H. Colledge

    (University of Cambridge)

  • Samuel A. J. R. Aparicio

    (Wellcome/CRC Institute for Cancer and Developmental Biology, University of Cambridge
    Paradigm Therapeutics Ltd
    Dep. of Oncology, Cambridge Institute of Medical Research, Addenbrookes' Hospital)

  • Mark B. L. Carlton

    (Wellcome/CRC Institute for Cancer and Developmental Biology, University of Cambridge
    University of Cambridge
    Paradigm Therapeutics Ltd)

  • Jonathan J. Pearce

    (Wellcome/CRC Institute for Cancer and Developmental Biology, University of Cambridge)

  • Sheila C. Barton

    (Wellcome/CRC Institute for Cancer and Developmental Biology, University of Cambridge)

  • M. Azim Surani

    (Wellcome/CRC Institute for Cancer and Developmental Biology, University of Cambridge)

  • Kenneth Ryan

    (Wellcome/CRC Institute for Cancer and Developmental Biology, University of Cambridge
    University of Pennsylvania School of Medicine)

  • Michael C. Nehls

    (Niedersächsisches Institut für Peptidforschung
    Ingenium Pharmaceuticals AG)

  • Valerie Wilson

    (Centre of Genome Research, University of Edinburgh, Kings Buildings)

  • Martin J. Evans

    (Wellcome/CRC Institute for Cancer and Developmental Biology, University of Cambridge
    Cardiff School of Biosciences)

Abstract

The earliest cell fate decision in the mammalian embryo separates the extra-embryonic trophoblast lineage, which forms the fetal portion of the placenta, from the embryonic cell lineages. The body plan of the embryo proper is established only later at gastrulation, when the pluripotent epiblast gives rise to the germ layers ectoderm, mesoderm and endoderm. Here we show that the T-box gene Eomesodermin1 performs essential functions in both trophoblast development and gastrulation. Mouse embryos lacking Eomesodermin arrest at the blastocyst stage. Mutant trophoectoderm does not differentiate into trophoblast, indicating that Eomesodermin may be required for the development of trophoblast stem cells2. In the embryo proper, Eomesodermin is essential for mesoderm formation. Although the specification of the anterior–posterior axis and the initial response to mesoderm-inducing signals is intact in mutant epiblasts, the prospective mesodermal cells are not recruited into the primitive streak. Our results indicate that Eomesodermin defines a conserved molecular pathway controlling the morphogenetic movements of germ layer formation and has acquired a new function in mammals in the differentiation of trophoblast.

Suggested Citation

  • Andreas P. Russ & Sigrid Wattler & William H. Colledge & Samuel A. J. R. Aparicio & Mark B. L. Carlton & Jonathan J. Pearce & Sheila C. Barton & M. Azim Surani & Kenneth Ryan & Michael C. Nehls & Vale, 2000. "Eomesodermin is required for mouse trophoblast development and mesoderm formation," Nature, Nature, vol. 404(6773), pages 95-99, March.
  • Handle: RePEc:nat:nature:v:404:y:2000:i:6773:d:10.1038_35003601
    DOI: 10.1038/35003601
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