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Establishment of a relationship between blastomere geometry and YAP localisation during compaction

Precise patterning within the three-dimensional context of tissues, organs and embryos implies that cells can sense their relative position. During preimplantation development, outside and inside cells rely on apicobasal polarity and the Hippo pathway to choose their fate. Despite recent findings su...

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Autores principales: Royer, Christophe, Leonavicius, Karolis, Kip, Annemarie, Fortin, Deborah, Nandi, Kirtirupa, Vincent, Anna, Jones, Celine, Child, Tim, Coward, Kevin, Graham, Chris, Srinivas, Shankar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7561472/
https://www.ncbi.nlm.nih.gov/pubmed/32928909
http://dx.doi.org/10.1242/dev.189449
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author Royer, Christophe
Leonavicius, Karolis
Kip, Annemarie
Fortin, Deborah
Nandi, Kirtirupa
Vincent, Anna
Jones, Celine
Child, Tim
Coward, Kevin
Graham, Chris
Srinivas, Shankar
author_facet Royer, Christophe
Leonavicius, Karolis
Kip, Annemarie
Fortin, Deborah
Nandi, Kirtirupa
Vincent, Anna
Jones, Celine
Child, Tim
Coward, Kevin
Graham, Chris
Srinivas, Shankar
author_sort Royer, Christophe
collection PubMed
description Precise patterning within the three-dimensional context of tissues, organs and embryos implies that cells can sense their relative position. During preimplantation development, outside and inside cells rely on apicobasal polarity and the Hippo pathway to choose their fate. Despite recent findings suggesting that mechanosensing might be central to this process, the relationship between blastomere geometry (i.e. shape and position) and the Hippo pathway effector YAP remains unknown. We used a highly quantitative approach to analyse information on the geometry and YAP localisation of individual blastomeres of mouse and human embryos. We identified the proportion of exposed cell surface area as most closely correlating with the nuclear localisation of YAP. To test this relationship, we developed several hydrogel-based approaches to alter blastomere geometry in cultured embryos. Unbiased clustering analyses of blastomeres from such embryos revealed that this relationship emerged during compaction. Our results therefore pinpoint the time during early embryogenesis when cells acquire the ability to sense changes in geometry and provide a new framework for how cells might integrate signals from different membrane domains to assess their relative position within the embryo.
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spelling pubmed-75614722020-10-20 Establishment of a relationship between blastomere geometry and YAP localisation during compaction Royer, Christophe Leonavicius, Karolis Kip, Annemarie Fortin, Deborah Nandi, Kirtirupa Vincent, Anna Jones, Celine Child, Tim Coward, Kevin Graham, Chris Srinivas, Shankar Development Research Article Precise patterning within the three-dimensional context of tissues, organs and embryos implies that cells can sense their relative position. During preimplantation development, outside and inside cells rely on apicobasal polarity and the Hippo pathway to choose their fate. Despite recent findings suggesting that mechanosensing might be central to this process, the relationship between blastomere geometry (i.e. shape and position) and the Hippo pathway effector YAP remains unknown. We used a highly quantitative approach to analyse information on the geometry and YAP localisation of individual blastomeres of mouse and human embryos. We identified the proportion of exposed cell surface area as most closely correlating with the nuclear localisation of YAP. To test this relationship, we developed several hydrogel-based approaches to alter blastomere geometry in cultured embryos. Unbiased clustering analyses of blastomeres from such embryos revealed that this relationship emerged during compaction. Our results therefore pinpoint the time during early embryogenesis when cells acquire the ability to sense changes in geometry and provide a new framework for how cells might integrate signals from different membrane domains to assess their relative position within the embryo. The Company of Biologists Ltd 2020-10-09 /pmc/articles/PMC7561472/ /pubmed/32928909 http://dx.doi.org/10.1242/dev.189449 Text en © 2020. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/4.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article
Royer, Christophe
Leonavicius, Karolis
Kip, Annemarie
Fortin, Deborah
Nandi, Kirtirupa
Vincent, Anna
Jones, Celine
Child, Tim
Coward, Kevin
Graham, Chris
Srinivas, Shankar
Establishment of a relationship between blastomere geometry and YAP localisation during compaction
title Establishment of a relationship between blastomere geometry and YAP localisation during compaction
title_full Establishment of a relationship between blastomere geometry and YAP localisation during compaction
title_fullStr Establishment of a relationship between blastomere geometry and YAP localisation during compaction
title_full_unstemmed Establishment of a relationship between blastomere geometry and YAP localisation during compaction
title_short Establishment of a relationship between blastomere geometry and YAP localisation during compaction
title_sort establishment of a relationship between blastomere geometry and yap localisation during compaction
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7561472/
https://www.ncbi.nlm.nih.gov/pubmed/32928909
http://dx.doi.org/10.1242/dev.189449
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