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

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...

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Autores principales: Posfai, Eszter, Petropoulos, Sophie, de Barros, Flavia Regina Oliveira, Schell, John Paul, Jurisica, Igor, Sandberg, Rickard, Lanner, Fredrik, Rossant, Janet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5370188/
https://www.ncbi.nlm.nih.gov/pubmed/28226240
http://dx.doi.org/10.7554/eLife.22906
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author Posfai, Eszter
Petropoulos, Sophie
de Barros, Flavia Regina Oliveira
Schell, John Paul
Jurisica, Igor
Sandberg, Rickard
Lanner, Fredrik
Rossant, Janet
author_facet Posfai, Eszter
Petropoulos, Sophie
de Barros, Flavia Regina Oliveira
Schell, John Paul
Jurisica, Igor
Sandberg, Rickard
Lanner, Fredrik
Rossant, Janet
author_sort Posfai, Eszter
collection PubMed
description 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. DOI: http://dx.doi.org/10.7554/eLife.22906.001
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spelling pubmed-53701882017-03-29 Position- and Hippo signaling-dependent plasticity during lineage segregation in the early mouse embryo Posfai, Eszter Petropoulos, Sophie de Barros, Flavia Regina Oliveira Schell, John Paul Jurisica, Igor Sandberg, Rickard Lanner, Fredrik Rossant, Janet eLife Developmental Biology and Stem Cells 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. DOI: http://dx.doi.org/10.7554/eLife.22906.001 eLife Sciences Publications, Ltd 2017-02-22 /pmc/articles/PMC5370188/ /pubmed/28226240 http://dx.doi.org/10.7554/eLife.22906 Text en © 2017, Posfai et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Developmental Biology and Stem Cells
Posfai, Eszter
Petropoulos, Sophie
de Barros, Flavia Regina Oliveira
Schell, John Paul
Jurisica, Igor
Sandberg, Rickard
Lanner, Fredrik
Rossant, Janet
Position- and Hippo signaling-dependent plasticity during lineage segregation in the early mouse embryo
title Position- and Hippo signaling-dependent plasticity during lineage segregation in the early mouse embryo
title_full Position- and Hippo signaling-dependent plasticity during lineage segregation in the early mouse embryo
title_fullStr Position- and Hippo signaling-dependent plasticity during lineage segregation in the early mouse embryo
title_full_unstemmed Position- and Hippo signaling-dependent plasticity during lineage segregation in the early mouse embryo
title_short Position- and Hippo signaling-dependent plasticity during lineage segregation in the early mouse embryo
title_sort position- and hippo signaling-dependent plasticity during lineage segregation in the early mouse embryo
topic Developmental Biology and Stem Cells
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5370188/
https://www.ncbi.nlm.nih.gov/pubmed/28226240
http://dx.doi.org/10.7554/eLife.22906
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