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Two mechanisms drive pronuclear migration in mouse zygotes
A new life begins with the unification of the maternal and paternal chromosomes upon fertilization. The parental chromosomes first become enclosed in two separate pronuclei near the surface of the fertilized egg. The mechanisms that then move the pronuclei inwards for their unification are only poor...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7864974/ https://www.ncbi.nlm.nih.gov/pubmed/33547291 http://dx.doi.org/10.1038/s41467-021-21020-x |
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author | Scheffler, Kathleen Uraji, Julia Jentoft, Ida Cavazza, Tommaso Mönnich, Eike Mogessie, Binyam Schuh, Melina |
author_facet | Scheffler, Kathleen Uraji, Julia Jentoft, Ida Cavazza, Tommaso Mönnich, Eike Mogessie, Binyam Schuh, Melina |
author_sort | Scheffler, Kathleen |
collection | PubMed |
description | A new life begins with the unification of the maternal and paternal chromosomes upon fertilization. The parental chromosomes first become enclosed in two separate pronuclei near the surface of the fertilized egg. The mechanisms that then move the pronuclei inwards for their unification are only poorly understood in mammals. Here, we report two mechanisms that act in concert to unite the parental genomes in fertilized mouse eggs. The male pronucleus assembles within the fertilization cone and is rapidly moved inwards by the flattening cone. Rab11a recruits the actin nucleation factors Spire and Formin-2 into the fertilization cone, where they locally nucleate actin and further accelerate the pronucleus inwards. In parallel, a dynamic network of microtubules assembles that slowly moves the male and female pronuclei towards the cell centre in a dynein-dependent manner. Both mechanisms are partially redundant and act in concert to unite the parental pronuclei in the zygote’s centre. |
format | Online Article Text |
id | pubmed-7864974 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78649742021-02-16 Two mechanisms drive pronuclear migration in mouse zygotes Scheffler, Kathleen Uraji, Julia Jentoft, Ida Cavazza, Tommaso Mönnich, Eike Mogessie, Binyam Schuh, Melina Nat Commun Article A new life begins with the unification of the maternal and paternal chromosomes upon fertilization. The parental chromosomes first become enclosed in two separate pronuclei near the surface of the fertilized egg. The mechanisms that then move the pronuclei inwards for their unification are only poorly understood in mammals. Here, we report two mechanisms that act in concert to unite the parental genomes in fertilized mouse eggs. The male pronucleus assembles within the fertilization cone and is rapidly moved inwards by the flattening cone. Rab11a recruits the actin nucleation factors Spire and Formin-2 into the fertilization cone, where they locally nucleate actin and further accelerate the pronucleus inwards. In parallel, a dynamic network of microtubules assembles that slowly moves the male and female pronuclei towards the cell centre in a dynein-dependent manner. Both mechanisms are partially redundant and act in concert to unite the parental pronuclei in the zygote’s centre. Nature Publishing Group UK 2021-02-05 /pmc/articles/PMC7864974/ /pubmed/33547291 http://dx.doi.org/10.1038/s41467-021-21020-x Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Scheffler, Kathleen Uraji, Julia Jentoft, Ida Cavazza, Tommaso Mönnich, Eike Mogessie, Binyam Schuh, Melina Two mechanisms drive pronuclear migration in mouse zygotes |
title | Two mechanisms drive pronuclear migration in mouse zygotes |
title_full | Two mechanisms drive pronuclear migration in mouse zygotes |
title_fullStr | Two mechanisms drive pronuclear migration in mouse zygotes |
title_full_unstemmed | Two mechanisms drive pronuclear migration in mouse zygotes |
title_short | Two mechanisms drive pronuclear migration in mouse zygotes |
title_sort | two mechanisms drive pronuclear migration in mouse zygotes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7864974/ https://www.ncbi.nlm.nih.gov/pubmed/33547291 http://dx.doi.org/10.1038/s41467-021-21020-x |
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