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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...

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Autores principales: Scheffler, Kathleen, Giannini, Federica, Lemonnier, Tom, Mogessie, Binyam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2022
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.
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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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