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A calcium‐mediated actin redistribution at egg activation in Drosophila
Egg activation is the essential process in which mature oocytes gain the competency to proceed into embryonic development. Many events of egg activation are conserved, including an initial rise of intracellular calcium. In some species, such as echinoderms and mammals, changes in the actin cytoskele...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7044060/ https://www.ncbi.nlm.nih.gov/pubmed/31880382 http://dx.doi.org/10.1002/mrd.23311 |
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author | York‐Andersen, Anna H. Hu, Qinan Wood, Benjamin W. Wolfner, Mariana F. Weil, Timothy T. |
author_facet | York‐Andersen, Anna H. Hu, Qinan Wood, Benjamin W. Wolfner, Mariana F. Weil, Timothy T. |
author_sort | York‐Andersen, Anna H. |
collection | PubMed |
description | Egg activation is the essential process in which mature oocytes gain the competency to proceed into embryonic development. Many events of egg activation are conserved, including an initial rise of intracellular calcium. In some species, such as echinoderms and mammals, changes in the actin cytoskeleton occur around the time of fertilization and egg activation. However, the interplay between calcium and actin during egg activation remains unclear. Here, we use imaging, genetics, pharmacological treatment, and physical manipulation to elucidate the relationship between calcium and actin in living Drosophila eggs. We show that, before egg activation, actin is smoothly distributed between ridges in the cortex of the dehydrated mature oocytes. At the onset of egg activation, we observe actin spreading out as the egg swells though the intake of fluid. We show that a relaxed actin cytoskeleton is required for the intracellular rise of calcium to initiate and propagate. Once the swelling is complete and the calcium wave is traversing the egg, it leads to a reorganization of actin in a wavelike manner. After the calcium wave, the actin cytoskeleton has an even distribution of foci at the cortex. Together, our data show that calcium resets the actin cytoskeleton at egg activation, a model that we propose to be likely conserved in other species. |
format | Online Article Text |
id | pubmed-7044060 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-70440602020-03-16 A calcium‐mediated actin redistribution at egg activation in Drosophila York‐Andersen, Anna H. Hu, Qinan Wood, Benjamin W. Wolfner, Mariana F. Weil, Timothy T. Mol Reprod Dev Research Articles Egg activation is the essential process in which mature oocytes gain the competency to proceed into embryonic development. Many events of egg activation are conserved, including an initial rise of intracellular calcium. In some species, such as echinoderms and mammals, changes in the actin cytoskeleton occur around the time of fertilization and egg activation. However, the interplay between calcium and actin during egg activation remains unclear. Here, we use imaging, genetics, pharmacological treatment, and physical manipulation to elucidate the relationship between calcium and actin in living Drosophila eggs. We show that, before egg activation, actin is smoothly distributed between ridges in the cortex of the dehydrated mature oocytes. At the onset of egg activation, we observe actin spreading out as the egg swells though the intake of fluid. We show that a relaxed actin cytoskeleton is required for the intracellular rise of calcium to initiate and propagate. Once the swelling is complete and the calcium wave is traversing the egg, it leads to a reorganization of actin in a wavelike manner. After the calcium wave, the actin cytoskeleton has an even distribution of foci at the cortex. Together, our data show that calcium resets the actin cytoskeleton at egg activation, a model that we propose to be likely conserved in other species. John Wiley and Sons Inc. 2019-12-27 2020-02 /pmc/articles/PMC7044060/ /pubmed/31880382 http://dx.doi.org/10.1002/mrd.23311 Text en © 2019 The Authors. Molecular Reproduction and Development published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles York‐Andersen, Anna H. Hu, Qinan Wood, Benjamin W. Wolfner, Mariana F. Weil, Timothy T. A calcium‐mediated actin redistribution at egg activation in Drosophila |
title | A calcium‐mediated actin redistribution at egg activation in Drosophila
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title_full | A calcium‐mediated actin redistribution at egg activation in Drosophila
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title_fullStr | A calcium‐mediated actin redistribution at egg activation in Drosophila
|
title_full_unstemmed | A calcium‐mediated actin redistribution at egg activation in Drosophila
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title_short | A calcium‐mediated actin redistribution at egg activation in Drosophila
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title_sort | calcium‐mediated actin redistribution at egg activation in drosophila |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7044060/ https://www.ncbi.nlm.nih.gov/pubmed/31880382 http://dx.doi.org/10.1002/mrd.23311 |
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