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Morphogenetic forces planar polarize LGN/Pins in the embryonic head during Drosophila gastrulation

Spindle orientation is often achieved by a complex of Partner of Inscuteable (Pins)/LGN, Mushroom Body Defect (Mud)/Nuclear Mitotic Apparatus (NuMa), Gαi, and Dynein, which interacts with astral microtubules to rotate the spindle. Cortical Pins/LGN recruitment serves as a critical step in this proce...

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Detalles Bibliográficos
Autores principales: Camuglia, Jaclyn, Chanet, Soline, Martin, Adam C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9262390/
https://www.ncbi.nlm.nih.gov/pubmed/35796436
http://dx.doi.org/10.7554/eLife.78779
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author Camuglia, Jaclyn
Chanet, Soline
Martin, Adam C
author_facet Camuglia, Jaclyn
Chanet, Soline
Martin, Adam C
author_sort Camuglia, Jaclyn
collection PubMed
description Spindle orientation is often achieved by a complex of Partner of Inscuteable (Pins)/LGN, Mushroom Body Defect (Mud)/Nuclear Mitotic Apparatus (NuMa), Gαi, and Dynein, which interacts with astral microtubules to rotate the spindle. Cortical Pins/LGN recruitment serves as a critical step in this process. Here, we identify Pins-mediated planar cell polarized divisions in several of the mitotic domains of the early Drosophila embryo. We found that neither planar cell polarity pathways nor planar polarized myosin localization determined division orientation; instead, our findings strongly suggest that Pins planar polarity and force generated from mesoderm invagination are important. Disrupting Pins polarity via overexpression of a myristoylated version of Pins caused randomized division angles. We found that disrupting forces through chemical inhibitors, depletion of an adherens junction protein, or blocking mesoderm invagination disrupted Pins planar polarity and spindle orientation. Furthermore, directional ablations that separated mesoderm from mitotic domains disrupted spindle orientation, suggesting that forces transmitted from mesoderm to mitotic domains can polarize Pins and orient division during gastrulation. To our knowledge, this is the first in vivo example where mechanical force has been shown to polarize Pins to mediate division orientation.
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spelling pubmed-92623902022-07-08 Morphogenetic forces planar polarize LGN/Pins in the embryonic head during Drosophila gastrulation Camuglia, Jaclyn Chanet, Soline Martin, Adam C eLife Cell Biology Spindle orientation is often achieved by a complex of Partner of Inscuteable (Pins)/LGN, Mushroom Body Defect (Mud)/Nuclear Mitotic Apparatus (NuMa), Gαi, and Dynein, which interacts with astral microtubules to rotate the spindle. Cortical Pins/LGN recruitment serves as a critical step in this process. Here, we identify Pins-mediated planar cell polarized divisions in several of the mitotic domains of the early Drosophila embryo. We found that neither planar cell polarity pathways nor planar polarized myosin localization determined division orientation; instead, our findings strongly suggest that Pins planar polarity and force generated from mesoderm invagination are important. Disrupting Pins polarity via overexpression of a myristoylated version of Pins caused randomized division angles. We found that disrupting forces through chemical inhibitors, depletion of an adherens junction protein, or blocking mesoderm invagination disrupted Pins planar polarity and spindle orientation. Furthermore, directional ablations that separated mesoderm from mitotic domains disrupted spindle orientation, suggesting that forces transmitted from mesoderm to mitotic domains can polarize Pins and orient division during gastrulation. To our knowledge, this is the first in vivo example where mechanical force has been shown to polarize Pins to mediate division orientation. eLife Sciences Publications, Ltd 2022-07-07 /pmc/articles/PMC9262390/ /pubmed/35796436 http://dx.doi.org/10.7554/eLife.78779 Text en © 2022, Camuglia et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Cell Biology
Camuglia, Jaclyn
Chanet, Soline
Martin, Adam C
Morphogenetic forces planar polarize LGN/Pins in the embryonic head during Drosophila gastrulation
title Morphogenetic forces planar polarize LGN/Pins in the embryonic head during Drosophila gastrulation
title_full Morphogenetic forces planar polarize LGN/Pins in the embryonic head during Drosophila gastrulation
title_fullStr Morphogenetic forces planar polarize LGN/Pins in the embryonic head during Drosophila gastrulation
title_full_unstemmed Morphogenetic forces planar polarize LGN/Pins in the embryonic head during Drosophila gastrulation
title_short Morphogenetic forces planar polarize LGN/Pins in the embryonic head during Drosophila gastrulation
title_sort morphogenetic forces planar polarize lgn/pins in the embryonic head during drosophila gastrulation
topic Cell Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9262390/
https://www.ncbi.nlm.nih.gov/pubmed/35796436
http://dx.doi.org/10.7554/eLife.78779
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