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Published May 8, 2018 | Published
Journal Article Open

Tracing the origin of heterogeneity and symmetry breaking in the early mammalian embryo

Abstract

A fundamental question in developmental and stem cell biology concerns the origin and nature of signals that initiate asymmetry leading to pattern formation and self-organization. Instead of having prominent pre-patterning determinants as present in model organisms (worms, sea urchin, frog), we propose that the mammalian embryo takes advantage of more subtle cues such as compartmentalized intracellular reactions that generate micro-scale inhomogeneity, which is gradually amplified over several cellular generations to drive pattern formation while keeping developmental plasticity. It is therefore possible that by making use of compartmentalized information followed by its amplification, mammalian embryos would follow general principle of development found in other organisms in which the spatial cue is more robustly presented.

Additional Information

© The Author(s) 2018. Open Access - This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. Received: 7 July 2017; Accepted: 6 April 2018. Published online: 08 May 2018. The work in MZG Lab is supported by grants from the ERC (669198) and the Wellcome Trust (098287/Z/12/Z) and in QC Lab by NIH (R01HD092431 and P30GM110767-03). We thank David Glover, Mubeen Goolam, and Xiudeng Zheng for feedback on the manuscript, and the members of our labs for suggestions. These authors contributed equally: Qi Chen, Junchao Shi. Author Contributions: M.Z.G., Q.C., and J.S. developed the concept and wrote the manuscript. Y.T. contributed to the mathematical aspects. The authors declare no competing interests.

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