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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2020
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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. |
format | Online Article Text |
id | pubmed-7561472 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
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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