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Publication : Position- and Hippo signaling-dependent plasticity during lineage segregation in the early mouse embryo.

First Author  Posfai E Year  2017
Journal  Elife Volume  6
PubMed ID  28226240 Mgi Jnum  J:242325
Mgi Id  MGI:5904917 Doi  10.7554/eLife.22906
Citation  Posfai E, et al. (2017) Position- and Hippo signaling-dependent plasticity during lineage segregation in the early mouse embryo. Elife 6:e22906
abstractText  The segregation of the trophectoderm (TE) from the inner cell mass (ICM) in the mouse blastocyst is determined by position-dependent Hippo signaling. However, the window of responsiveness to Hippo signaling, the exact timing of lineage commitment and the overall relationship between cell commitment and global gene expression changes are still unclear. Single-cell RNA sequencing during lineage segregation revealed that the TE transcriptional profile stabilizes earlier than the ICM and prior to blastocyst formation. Using quantitative Cdx2-eGFP expression as a readout of Hippo signaling activity, we assessed the experimental potential of individual blastomeres based on their level of Cdx2-eGFP expression and correlated potential with gene expression dynamics. We find that TE specification and commitment coincide and occur at the time of transcriptional stabilization, whereas ICM cells still retain the ability to regenerate TE up to the early blastocyst stage. Plasticity of both lineages is coincident with their window of sensitivity to Hippo signaling.
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