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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...

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Autores principales: Liu, Chenshu, Rex, Rachel, Lung, Zoe, Wang, John S., Wu, Fan, Kim, Hyung Jun, Zhang, Liangyu, Sohn, Lydia L., Dernburg, Abby F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2023
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.
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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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