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A cooperative network at the nuclear envelope counteracts LINC-mediated forces during oogenesis in C. elegans
Oogenesis involves transduction of mechanical forces from the cytoskeleton to the nuclear envelope (NE). In Caenorhabditis elegans, oocyte nuclei lacking the single lamin protein LMN-1 are vulnerable to collapse under forces mediated through LINC (linker of nucleoskeleton and cytoskeleton) complexes...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10337908/ https://www.ncbi.nlm.nih.gov/pubmed/37436986 http://dx.doi.org/10.1126/sciadv.abn5709 |
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author | Liu, Chenshu Rex, Rachel Lung, Zoe Wang, John S. Wu, Fan Kim, Hyung Jun Zhang, Liangyu Sohn, Lydia L. Dernburg, Abby F. |
author_facet | Liu, Chenshu Rex, Rachel Lung, Zoe Wang, John S. Wu, Fan Kim, Hyung Jun Zhang, Liangyu Sohn, Lydia L. Dernburg, Abby F. |
author_sort | Liu, Chenshu |
collection | PubMed |
description | Oogenesis involves transduction of mechanical forces from the cytoskeleton to the nuclear envelope (NE). In Caenorhabditis elegans, oocyte nuclei lacking the single lamin protein LMN-1 are vulnerable to collapse under forces mediated through LINC (linker of nucleoskeleton and cytoskeleton) complexes. Here, we use cytological analysis and in vivo imaging to investigate the balance of forces that drive this collapse and protect oocyte nuclei. We also use a mechano-node-pore sensing device to directly measure the effect of genetic mutations on oocyte nuclear stiffness. We find that nuclear collapse is not a consequence of apoptosis. It is promoted by dynein, which induces polarization of a LINC complex composed of Sad1 and UNC-84 homology 1 (SUN-1) and ZYGote defective 12 (ZYG-12). Lamins contribute to oocyte nuclear stiffness and cooperate with other inner nuclear membrane proteins to distribute LINC complexes and protect nuclei from collapse. We speculate that a similar network may protect oocyte integrity during extended oocyte arrest in mammals. |
format | Online Article Text |
id | pubmed-10337908 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-103379082023-07-13 A cooperative network at the nuclear envelope counteracts LINC-mediated forces during oogenesis in C. elegans Liu, Chenshu Rex, Rachel Lung, Zoe Wang, John S. Wu, Fan Kim, Hyung Jun Zhang, Liangyu Sohn, Lydia L. Dernburg, Abby F. Sci Adv Biomedicine and Life Sciences Oogenesis involves transduction of mechanical forces from the cytoskeleton to the nuclear envelope (NE). In Caenorhabditis elegans, oocyte nuclei lacking the single lamin protein LMN-1 are vulnerable to collapse under forces mediated through LINC (linker of nucleoskeleton and cytoskeleton) complexes. Here, we use cytological analysis and in vivo imaging to investigate the balance of forces that drive this collapse and protect oocyte nuclei. We also use a mechano-node-pore sensing device to directly measure the effect of genetic mutations on oocyte nuclear stiffness. We find that nuclear collapse is not a consequence of apoptosis. It is promoted by dynein, which induces polarization of a LINC complex composed of Sad1 and UNC-84 homology 1 (SUN-1) and ZYGote defective 12 (ZYG-12). Lamins contribute to oocyte nuclear stiffness and cooperate with other inner nuclear membrane proteins to distribute LINC complexes and protect nuclei from collapse. We speculate that a similar network may protect oocyte integrity during extended oocyte arrest in mammals. American Association for the Advancement of Science 2023-07-12 /pmc/articles/PMC10337908/ /pubmed/37436986 http://dx.doi.org/10.1126/sciadv.abn5709 Text en Copyright © 2023 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution License 4.0 (CC BY). https://creativecommons.org/licenses/by/4.0/This 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 the original work is properly cited. |
spellingShingle | Biomedicine and Life Sciences Liu, Chenshu Rex, Rachel Lung, Zoe Wang, John S. Wu, Fan Kim, Hyung Jun Zhang, Liangyu Sohn, Lydia L. Dernburg, Abby F. A cooperative network at the nuclear envelope counteracts LINC-mediated forces during oogenesis in C. elegans |
title | A cooperative network at the nuclear envelope counteracts LINC-mediated forces during oogenesis in C. elegans |
title_full | A cooperative network at the nuclear envelope counteracts LINC-mediated forces during oogenesis in C. elegans |
title_fullStr | A cooperative network at the nuclear envelope counteracts LINC-mediated forces during oogenesis in C. elegans |
title_full_unstemmed | A cooperative network at the nuclear envelope counteracts LINC-mediated forces during oogenesis in C. elegans |
title_short | A cooperative network at the nuclear envelope counteracts LINC-mediated forces during oogenesis in C. elegans |
title_sort | cooperative network at the nuclear envelope counteracts linc-mediated forces during oogenesis in c. elegans |
topic | Biomedicine and Life Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10337908/ https://www.ncbi.nlm.nih.gov/pubmed/37436986 http://dx.doi.org/10.1126/sciadv.abn5709 |
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