RanGTP and the actin cytoskeleton keep paternal and maternal chromosomes apart during fertilization.


Journal

The Journal of cell biology
ISSN: 1540-8140
Titre abrégé: J Cell Biol
Pays: United States
ID NLM: 0375356

Informations de publication

Date de publication:
04 10 2021
Historique:
received: 01 12 2020
revised: 18 06 2021
accepted: 06 08 2021
entrez: 23 8 2021
pubmed: 24 8 2021
medline: 1 12 2021
Statut: ppublish

Résumé

Zygotes require two accurate sets of parental chromosomes, one each from the mother and the father, to undergo normal embryogenesis. However, upon egg-sperm fusion in vertebrates, the zygote has three sets of chromosomes, one from the sperm and two from the egg. The zygote therefore eliminates one set of maternal chromosomes (but not the paternal chromosomes) into the polar body through meiosis, but how the paternal chromosomes are protected from maternal meiosis has been unclear. Here we report that RanGTP and F-actin dynamics prevent egg-sperm fusion in proximity to maternal chromosomes. RanGTP prevents the localization of Juno and CD9, egg membrane proteins that mediate sperm fusion, at the cell surface in proximity to maternal chromosomes. Following egg-sperm fusion, F-actin keeps paternal chromosomes away from maternal chromosomes. Disruption of these mechanisms causes the elimination of paternal chromosomes during maternal meiosis. This study reveals a novel critical mechanism that prevents aneuploidy in zygotes.

Identifiants

pubmed: 34424312
pii: 212591
doi: 10.1083/jcb.202012001
pmc: PMC8404465
pii:
doi:

Substances chimiques

ran GTP-Binding Protein EC 3.6.5.2

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Bill & Melinda Gates Foundation
ID : INV-001902
Pays : United States

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2021 Mori et al.

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Auteurs

Masashi Mori (M)

Research Institute for Microbial Diseases, Osaka University, Osaka, Japan.
Laboratory for Chromosome Segregation, RIKEN Center for Biosystems Dynamics Research, Kobe, Japan.

Tatsuma Yao (T)

Research and Development Center, Fuso Pharmaceutical Industries, Ltd., Osaka, Japan.
Graduate School of Biology-Oriented Science and Technology, Kindai University, Wakayama, Japan.

Tappei Mishina (T)

Laboratory for Chromosome Segregation, RIKEN Center for Biosystems Dynamics Research, Kobe, Japan.

Hiromi Endoh (H)

Laboratory for Ultrastructural Research, RIKEN Center for Biosystems Dynamics Research, Kobe, Japan.

Masahito Tanaka (M)

Physics and Cell Biology Laboratory, National Institute of Genetics & Department of Genetics, SOKENDAI University, Kanagawa, Japan.

Nao Yonezawa (N)

Graduate School of Biology-Oriented Science and Technology, Kindai University, Wakayama, Japan.

Yuta Shimamoto (Y)

Physics and Cell Biology Laboratory, National Institute of Genetics & Department of Genetics, SOKENDAI University, Kanagawa, Japan.

Shigenobu Yonemura (S)

Laboratory for Ultrastructural Research, RIKEN Center for Biosystems Dynamics Research, Kobe, Japan.
Department of Cell Biology, Tokushima University Graduate School of Medical Science, Tokushima, Japan.

Kazuo Yamagata (K)

Graduate School of Biology-Oriented Science and Technology, Kindai University, Wakayama, Japan.

Tomoya S Kitajima (TS)

Laboratory for Chromosome Segregation, RIKEN Center for Biosystems Dynamics Research, Kobe, Japan.

Masahito Ikawa (M)

Research Institute for Microbial Diseases, Osaka University, Osaka, Japan.

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