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Polychaetoid/ZO-1 strengthens cell junctions under tension while localizing differently than core adherens junction proteins
During embryonic development dramatic cell shape changes and movements re-shape the embryonic body plan. These require robust but dynamic linkage between the cell-cell adherens junctions and the force-generating actomyosin cytoskeleton. Our view of this linkage has evolved, and we now realize linkag...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10002719/ https://www.ncbi.nlm.nih.gov/pubmed/36909597 http://dx.doi.org/10.1101/2023.03.01.530634 |
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author | Schmidt, Anja Finegan, Tara Häring, Matthias Kong, Deqing Fletcher, Alexander G Alam, Zuhayr Grosshans, Jörg Wolf, Fred Peifer, Mark |
author_facet | Schmidt, Anja Finegan, Tara Häring, Matthias Kong, Deqing Fletcher, Alexander G Alam, Zuhayr Grosshans, Jörg Wolf, Fred Peifer, Mark |
author_sort | Schmidt, Anja |
collection | PubMed |
description | During embryonic development dramatic cell shape changes and movements re-shape the embryonic body plan. These require robust but dynamic linkage between the cell-cell adherens junctions and the force-generating actomyosin cytoskeleton. Our view of this linkage has evolved, and we now realize linkage is mediated by a mechanosensitive multiprotein complex assembled via multivalent connections. Here we combine genetic, cell biological and modeling approaches to define the mechanism of action and functions of an important player, Drosophila Polychaetoid, homolog of mammalian ZO-1. Our data reveal that Pyd reinforces cell junctions under elevated tension, and facilitates cell rearrangements. Pyd is important to maintain junctional contractility and in its absence cell rearrangements stall. We next use structured illumination microscopy to define the molecular architecture of cell-cell junctions during these events. The cadherin-catenin complex and Cno both localize to puncta along the junctional membrane, but are differentially enriched in different puncta. Pyd, in contrast, exhibits a distinct localization to strands that extend out from the region occupied by core junction proteins. We then discuss the implications for the protein network at the junction-cytoskeletal interface, suggesting different proteins localize and function in distinct ways but combine to produce robust connections. |
format | Online Article Text |
id | pubmed-10002719 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-100027192023-03-11 Polychaetoid/ZO-1 strengthens cell junctions under tension while localizing differently than core adherens junction proteins Schmidt, Anja Finegan, Tara Häring, Matthias Kong, Deqing Fletcher, Alexander G Alam, Zuhayr Grosshans, Jörg Wolf, Fred Peifer, Mark bioRxiv Article During embryonic development dramatic cell shape changes and movements re-shape the embryonic body plan. These require robust but dynamic linkage between the cell-cell adherens junctions and the force-generating actomyosin cytoskeleton. Our view of this linkage has evolved, and we now realize linkage is mediated by a mechanosensitive multiprotein complex assembled via multivalent connections. Here we combine genetic, cell biological and modeling approaches to define the mechanism of action and functions of an important player, Drosophila Polychaetoid, homolog of mammalian ZO-1. Our data reveal that Pyd reinforces cell junctions under elevated tension, and facilitates cell rearrangements. Pyd is important to maintain junctional contractility and in its absence cell rearrangements stall. We next use structured illumination microscopy to define the molecular architecture of cell-cell junctions during these events. The cadherin-catenin complex and Cno both localize to puncta along the junctional membrane, but are differentially enriched in different puncta. Pyd, in contrast, exhibits a distinct localization to strands that extend out from the region occupied by core junction proteins. We then discuss the implications for the protein network at the junction-cytoskeletal interface, suggesting different proteins localize and function in distinct ways but combine to produce robust connections. Cold Spring Harbor Laboratory 2023-03-01 /pmc/articles/PMC10002719/ /pubmed/36909597 http://dx.doi.org/10.1101/2023.03.01.530634 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Schmidt, Anja Finegan, Tara Häring, Matthias Kong, Deqing Fletcher, Alexander G Alam, Zuhayr Grosshans, Jörg Wolf, Fred Peifer, Mark Polychaetoid/ZO-1 strengthens cell junctions under tension while localizing differently than core adherens junction proteins |
title | Polychaetoid/ZO-1 strengthens cell junctions under tension while localizing differently than core adherens junction proteins |
title_full | Polychaetoid/ZO-1 strengthens cell junctions under tension while localizing differently than core adherens junction proteins |
title_fullStr | Polychaetoid/ZO-1 strengthens cell junctions under tension while localizing differently than core adherens junction proteins |
title_full_unstemmed | Polychaetoid/ZO-1 strengthens cell junctions under tension while localizing differently than core adherens junction proteins |
title_short | Polychaetoid/ZO-1 strengthens cell junctions under tension while localizing differently than core adherens junction proteins |
title_sort | polychaetoid/zo-1 strengthens cell junctions under tension while localizing differently than core adherens junction proteins |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10002719/ https://www.ncbi.nlm.nih.gov/pubmed/36909597 http://dx.doi.org/10.1101/2023.03.01.530634 |
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