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Nodal signalling in the epiblast patterns the early mouse embryo

Author

Listed:
  • Jane Brennan

    (Harvard University)

  • Cindy C. Lu

    (Harvard University)

  • Dominic P. Norris

    (Harvard University)

  • Tristan A. Rodriguez

    (National Institute for Medical Research)

  • Rosa S. P. Beddington

    (National Institute for Medical Research)

  • Elizabeth J. Robertson

    (Harvard University)

Abstract

Shortly after implantation the mouse embryo comprises three tissue layers. The founder tissue of the embryo proper, the epiblast, forms a radially symmetric cup of epithelial cells that grows in close apposition to the extra-embryonic ectoderm and the visceral endoderm. This simple cylindrical structure exhibits a distinct molecular pattern along its proximal–distal axis1. The anterior–posterior axis of the embryo is positioned later by coordinated cell movements that rotate the pre-existing proximal–distal axis2,3,4,5. The transforming growth factor-β family member Nodal is known to be required for formation of the anterior–posterior axis6. Here we show that signals from the epiblast are responsible for the initiation of proximal–distal polarity. Nodal acts to promote posterior cell fates in the epiblast and to maintain molecular pattern in the adjacent extra-embryonic ectoderm. Both of these functions are independent of Smad2. Moreover, Nodal signals from the epiblast also pattern the visceral endoderm by activating the Smad2-dependent pathway required for specification of anterior identity in overlying epiblast cells. Our experiments show that proximal–distal and subsequent anterior–posterior polarity of the pregastrulation embryo result from reciprocal cell–cell interactions between the epiblast and the two extra-embryonic tissues.

Suggested Citation

  • Jane Brennan & Cindy C. Lu & Dominic P. Norris & Tristan A. Rodriguez & Rosa S. P. Beddington & Elizabeth J. Robertson, 2001. "Nodal signalling in the epiblast patterns the early mouse embryo," Nature, Nature, vol. 411(6840), pages 965-969, June.
  • Handle: RePEc:nat:nature:v:411:y:2001:i:6840:d:10.1038_35082103
    DOI: 10.1038/35082103
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    Cited by:

    1. Thomas Legier & Diane Rattier & Jack Llewellyn & Thomas Vannier & Benoit Sorre & Flavio Maina & Rosanna Dono, 2023. "Epithelial disruption drives mesendoderm differentiation in human pluripotent stem cells by enabling TGF-β protein sensing," Nature Communications, Nature, vol. 14(1), pages 1-18, December.
    2. Haipeng Fu & Tingyu Wang & Xiaohui Kong & Kun Yan & Yang Yang & Jingyi Cao & Yafei Yuan & Nan Wang & Kehkooi Kee & Zhi John Lu & Qiaoran Xi, 2022. "A Nodal enhanced micropeptide NEMEP regulates glucose uptake during mesendoderm differentiation of embryonic stem cells," Nature Communications, Nature, vol. 13(1), pages 1-17, December.
    3. Sina Schumacher & Max Fernkorn & Michelle Marten & Rui Chen & Yung Su Kim & Ivan Bedzhov & Christian Schröter, 2024. "Tissue-intrinsic beta-catenin signals antagonize Nodal-driven anterior visceral endoderm differentiation," Nature Communications, Nature, vol. 15(1), pages 1-15, December.

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