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Regulation of long-range BMP gradients and embryonic polarity by propagation of local calcium-firing activity.

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Peer-reviewed

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Abstract

Many amniote vertebrate species including humans can form identical twins from a single embryo, but this only occurs rarely. It has been suggested that the primitive-streak-forming embryonic region emits signals that inhibit streak formation elsewhere but the signals involved, how they are transmitted and how they act has not been elucidated. Here we show that short tracks of calcium firing activity propagate through extraembryonic tissue via gap junctions and prevent ectopic primitive streak formation in chick embryos. Cross-regulation of calcium activity and an inhibitor of primitive streak formation (Bone Morphogenetic Protein, BMP) via NF-κB and NFAT establishes a long-range BMP gradient spanning the embryo. This mechanism explains how embryos of widely different sizes can maintain positional information that determines embryo polarity. We provide evidence for similar mechanisms in two different human embryo models and in Drosophila, suggesting an ancient evolutionary origin.

Description

Acknowledgements: We are grateful to Sandip Patel, Anant Parekh, Andrea Streit and Octavian Voiculescu for advice on experiments and helpful comments on the manuscript. We also acknowledge the Cell Services Science Technology Platform at the Francis Crick Institute for providing regular Mycoplasma screening of the hESC line, the Zoology Imaging Facility of Cambridge University for assistance and support with microscopy on Drosophila embryos, and Sophie Brumm for providing a pSMAD staining protocol. This study was funded by a Wellcome Trust Investigator Award (107055/Z/15/Z) to C.D.S., which supported H.C.L., H.-C.L. and N.M.M.O. H.C.L. was also supported by a fellowship from the Basic Science Research Program through the National Research Foundation of Korea (NRF) (2014R1A6A3A03053468). N.M.M.O. was also funded by UCL. C.H. was funded by a Medical Research Council Doctoral Training Programme studentship (MR/N013867/1). P.B.-B. and N.M. were funded by the Francis Crick Institute which receives its core funding from Cancer Research UK (CC2186), the UK Medical Research Council (CC2186), and the Wellcome Trust (CC2186). A.A.M. was funded by a studentship from the Anatomical Society of Great Britain and Ireland in C.D.S.’s lab. Y.Z. and J.F. were funded by the Michigan-Cambridge Research Initiative, the US National Institutes of Health (R21 HD100931), and the National Science Foundation (CMMI 1917304). E.L.W. was funded by a BBSRC DTP scholarship. T.T.W. was funded by the University of Cambridge ISSF (097814) and the Wellcome Trust (200734/Z/16/Z).


Funder: Anatomical Society of Great Britain and Ireland. PhD studentship


Funder: Michigan-Cambridge Research Initiative


Funder: U.S. Department of Health & Human Services | NIH | Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

Journal Title

Nat Commun

Conference Name

Journal ISSN

2041-1723
2041-1723

Volume Title

15

Publisher

Springer Nature

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Except where otherwised noted, this item's license is described as Attribution 4.0 International
Sponsorship
Wellcome Trust (200734/Z/16/Z)
Wellcome Trust (097814/Z/11/Z)