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The prophase oocyte nucleus is a homeostatic G-actin buffer
Formation of healthy mammalian eggs from oocytes requires specialised F-actin structures. F-actin disruption produces aneuploid eggs, which are a leading cause of human embryo deaths, genetic disorders and infertility. We found that oocytes contain prominent nuclear F-actin structures that are corre...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8977058/ https://www.ncbi.nlm.nih.gov/pubmed/35112707 http://dx.doi.org/10.1242/jcs.259807 |
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author | Scheffler, Kathleen Giannini, Federica Lemonnier, Tom Mogessie, Binyam |
author_facet | Scheffler, Kathleen Giannini, Federica Lemonnier, Tom Mogessie, Binyam |
author_sort | Scheffler, Kathleen |
collection | PubMed |
description | Formation of healthy mammalian eggs from oocytes requires specialised F-actin structures. F-actin disruption produces aneuploid eggs, which are a leading cause of human embryo deaths, genetic disorders and infertility. We found that oocytes contain prominent nuclear F-actin structures that are correlated with meiotic developmental capacity. We demonstrate that nuclear F-actin is a conserved feature of healthy mammalian oocytes and declines significantly with female reproductive ageing. Actin monomers used for nuclear F-actin assembly are sourced from an excess pool in the oocyte cytoplasm. Increasing monomeric G-actin transfer from the cytoplasm to the nucleus or directly enriching the nucleus with monomers led to assembly of stable nuclear F-actin bundles that significantly restrict chromatin mobility. By contrast, reducing G-actin monomer transfer by blocking nuclear import triggered assembly of a dense cytoplasmic F-actin network that is incompatible with healthy oocyte development. Overall, our data suggest that the large oocyte nucleus helps to maintain cytoplasmic F-actin organisation and that defects in this function are linked with reproductive age-related female infertility. This article has an associated First Person interview with Federica Giannini, joint first author of the paper. |
format | Online Article Text |
id | pubmed-8977058 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-89770582022-04-25 The prophase oocyte nucleus is a homeostatic G-actin buffer Scheffler, Kathleen Giannini, Federica Lemonnier, Tom Mogessie, Binyam J Cell Sci Research Article Formation of healthy mammalian eggs from oocytes requires specialised F-actin structures. F-actin disruption produces aneuploid eggs, which are a leading cause of human embryo deaths, genetic disorders and infertility. We found that oocytes contain prominent nuclear F-actin structures that are correlated with meiotic developmental capacity. We demonstrate that nuclear F-actin is a conserved feature of healthy mammalian oocytes and declines significantly with female reproductive ageing. Actin monomers used for nuclear F-actin assembly are sourced from an excess pool in the oocyte cytoplasm. Increasing monomeric G-actin transfer from the cytoplasm to the nucleus or directly enriching the nucleus with monomers led to assembly of stable nuclear F-actin bundles that significantly restrict chromatin mobility. By contrast, reducing G-actin monomer transfer by blocking nuclear import triggered assembly of a dense cytoplasmic F-actin network that is incompatible with healthy oocyte development. Overall, our data suggest that the large oocyte nucleus helps to maintain cytoplasmic F-actin organisation and that defects in this function are linked with reproductive age-related female infertility. This article has an associated First Person interview with Federica Giannini, joint first author of the paper. The Company of Biologists Ltd 2022-03-23 /pmc/articles/PMC8977058/ /pubmed/35112707 http://dx.doi.org/10.1242/jcs.259807 Text en © 2022. Published by The Company of Biologists Ltd 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 that the original work is properly attributed. |
spellingShingle | Research Article Scheffler, Kathleen Giannini, Federica Lemonnier, Tom Mogessie, Binyam The prophase oocyte nucleus is a homeostatic G-actin buffer |
title | The prophase oocyte nucleus is a homeostatic G-actin buffer |
title_full | The prophase oocyte nucleus is a homeostatic G-actin buffer |
title_fullStr | The prophase oocyte nucleus is a homeostatic G-actin buffer |
title_full_unstemmed | The prophase oocyte nucleus is a homeostatic G-actin buffer |
title_short | The prophase oocyte nucleus is a homeostatic G-actin buffer |
title_sort | prophase oocyte nucleus is a homeostatic g-actin buffer |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8977058/ https://www.ncbi.nlm.nih.gov/pubmed/35112707 http://dx.doi.org/10.1242/jcs.259807 |
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