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      Nuclear F-actin and Lamin A antagonistically modulate nuclear shape

      research-article
      , * ,
      Journal of Cell Science
      The Company of Biologists Ltd
      HeLa, Lamin A, Xenopus, Actin, Formins, Nuclear shape

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          ABSTRACT

          Nuclear shape influences cell migration, gene expression and cell cycle progression, and is altered in disease states like laminopathies and cancer. What factors and forces determine nuclear shape? We find that nuclei assembled in Xenopus egg extracts in the presence of dynamic F-actin exhibit a striking bilobed nuclear morphology with distinct membrane compositions in the two lobes and accumulation of F-actin at the inner nuclear envelope. The addition of Lamin A (encoded by lmna), which is absent from Xenopus eggs, results in rounder nuclei, suggesting that opposing nuclear F-actin and Lamin A forces contribute to the regulation of nuclear shape. Nuclear F-actin also promotes altered nuclear shape in Lamin A-knockdown HeLa cells and, in both systems, abnormal nuclear shape is driven by formins and not Arp2/3 or myosin. Although the underlying mechanisms might differ in Xenopus and HeLa cells, we propose that nuclear F-actin filaments nucleated by formins impart outward forces that lead to altered nuclear morphology unless Lamin A is present. Targeting nuclear actin dynamics might represent a novel approach to rescuing disease-associated defects in nuclear shape.

          Abstract

          Summary: Formin-nucleated F-actin and Lamin A antagonistically modulate nuclear shape in Xenopus egg extracts and HeLa cells, which might be relevant in diseases with altered nuclear morphology.

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          Most cited references94

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          Nuclear envelope rupture and repair during cancer cell migration.

          During cancer metastasis, tumor cells penetrate tissues through tight interstitial spaces, which requires extensive deformation of the cell and its nucleus. Here, we investigated mammalian tumor cell migration in confining microenvironments in vitro and in vivo. Nuclear deformation caused localized loss of nuclear envelope (NE) integrity, which led to the uncontrolled exchange of nucleo-cytoplasmic content, herniation of chromatin across the NE, and DNA damage. The incidence of NE rupture increased with cell confinement and with depletion of nuclear lamins, NE proteins that structurally support the nucleus. Cells restored NE integrity using components of the endosomal sorting complexes required for transport III (ESCRT III) machinery. Our findings indicate that cell migration incurs substantial physical stress on the NE and its content and requires efficient NE and DNA damage repair for cell survival.
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            A major developmental transition in early Xenopus embryos: I. characterization and timing of cellular changes at the midblastula stage.

            The Xenopus embryo undergoes 12 rapid synchronous cleavages followed by a period of slower asynchronous divisions more typical of somatic cells. This change in cell cleavage has been termed the midblastula transition (MBT). We show that at the MBT the blastomeres become motile and transcriptionally active for the first time. We have investigated the timing of the MBT and found that it does not depend on cell division, on time since fertilization or on a counting mechanism involving the sequential modification of DNA. Rather, the timing of the MBT depends on reaching a critical ratio of nucleus to cytoplasm. We view the MBT as a consequence of the titration of some substance, originally present in the egg, by the exponentially increasing nuclear material. When this substance is exhausted a new cell program is engaged, leading to the acquisition of several new cell properties.
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              ESCRT III repairs nuclear envelope ruptures during cell migration to limit DNA damage and cell death.

              In eukaryotic cells, the nuclear envelope separates the genomic DNA from the cytoplasmic space and regulates protein trafficking between the two compartments. This barrier is only transiently dissolved during mitosis. Here, we found that it also opened at high frequency in migrating mammalian cells during interphase, which allowed nuclear proteins to leak out and cytoplasmic proteins to leak in. This transient opening was caused by nuclear deformation and was rapidly repaired in an ESCRT (endosomal sorting complexes required for transport)-dependent manner. DNA double-strand breaks coincided with nuclear envelope opening events. As a consequence, survival of cells migrating through confining environments depended on efficient nuclear envelope and DNA repair machineries. Nuclear envelope opening in migrating leukocytes could have potentially important consequences for normal and pathological immune responses.
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                Author and article information

                Contributors
                Journal
                J Cell Sci
                J Cell Sci
                JCS
                Journal of Cell Science
                The Company of Biologists Ltd
                0021-9533
                1477-9137
                1 July 2022
                4 July 2022
                4 July 2022
                : 135
                : 13
                : jcs259692
                Affiliations
                Department of Molecular Biology, University of Wyoming , Laramie, WY 82071, USA
                Author notes
                [* ]Author for correspondence ( dlevy1@ 123456uwyo.edu )

                Handling Editor: Maria Carmo-Fonseca

                Competing interests

                The authors declare no competing or financial interests.

                Author information
                http://orcid.org/0000-0002-7853-3275
                Article
                JCS259692
                10.1242/jcs.259692
                9377710
                35665815
                599f0756-0fd9-4a51-b79c-694c3ba1b73e
                © 2022. Published by The Company of Biologists Ltd

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.

                History
                : 15 December 2021
                : 28 May 2022
                Funding
                Funded by: National Institutes of Health, http://dx.doi.org/10.13039/100000002;
                Funded by: National Institute of General Medical Sciences, http://dx.doi.org/10.13039/100000057;
                Award ID: R35GM134885
                Award ID: P20GM103432
                Funded by: National Institute of Food and Agriculture, http://dx.doi.org/10.13039/100005825;
                Award ID: 1012152
                Funded by: University of Wyoming , http://dx.doi.org/10.13039/100008106;
                Categories
                Research Article

                Cell biology
                hela,lamin a,xenopus,actin,formins,nuclear shape
                Cell biology
                hela, lamin a, xenopus, actin, formins, nuclear shape

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