Phenogenetics of cortical granule dynamics during zebrafish oocyte-to-embryo transition

Fertilization is a critical process in sexual reproduction that involves the fusion of a capacitated sperm with a mature oocyte to form a zygote. Polyspermy, the fertilization of an oocyte by multiple sperm, leads to polyploidy and embryo lethality. Mammalian and non-mammalian oocytes have evolved m...

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Main Authors: Priscila García-Castro, Isabella Giambó-Falian, Ingrid Carvacho, Ricardo Fuentes
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-01-01
Series:Frontiers in Cell and Developmental Biology
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Online Access:https://www.frontiersin.org/articles/10.3389/fcell.2025.1514461/full
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author Priscila García-Castro
Isabella Giambó-Falian
Ingrid Carvacho
Ricardo Fuentes
author_facet Priscila García-Castro
Isabella Giambó-Falian
Ingrid Carvacho
Ricardo Fuentes
author_sort Priscila García-Castro
collection DOAJ
description Fertilization is a critical process in sexual reproduction that involves the fusion of a capacitated sperm with a mature oocyte to form a zygote. Polyspermy, the fertilization of an oocyte by multiple sperm, leads to polyploidy and embryo lethality. Mammalian and non-mammalian oocytes have evolved mechanisms to prevent polyspermy, including fast and slow blocks. The fast block comprises membrane depolarization post-sperm fusion, temporarily preventing additional sperm fusion. The slow block, triggered by cortical granule (CG) exocytosis, involves the release of proteins that modify the zona pellucida to form a permanent barrier, avoiding the fertilization by additional sperm. The evidence shows that immature oocytes often fail to prevent polyspermy due to ineffective CG exocytosis, attributed to impaired intracellular calcium increases, lower content of this ion, and incomplete CG migration. The study of how genetic variations lead to observable phenotypes (phenogenetics) during the oocyte-to-embryo transition, have identified several maternal-effect genes in zebrafish involved in CG behavior. These genes regulate various stages of CG biology, including biosynthesis, maturation, and exocytosis. Mutations in these genes disrupt these processes, highlighting the maternal genetic control over CG properties. Zebrafish has emerged as a pivotal model for understanding the evolving genetic regulation and molecular mechanisms underlying CG biology, providing valuable insights into fertility and early embryonic development.
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spelling doaj-art-4fc1c861abff4bd391bf61169694c8c02025-01-30T06:22:39ZengFrontiers Media S.A.Frontiers in Cell and Developmental Biology2296-634X2025-01-011310.3389/fcell.2025.15144611514461Phenogenetics of cortical granule dynamics during zebrafish oocyte-to-embryo transitionPriscila García-Castro0Isabella Giambó-Falian1Ingrid Carvacho2Ricardo Fuentes3Laboratorio de Fenómica y Embriogénesis Temprana (LAFET), Departamento de Biología Celular, Facultad de Ciencias Biológicas, Universidad de Concepción, Concepción, ChileLaboratorio de Fenómica y Embriogénesis Temprana (LAFET), Departamento de Biología Celular, Facultad de Ciencias Biológicas, Universidad de Concepción, Concepción, ChileLaboratorio de Canales Iónicos y Reproducción (CIR), Departamento de Medicina Translacional, Facultad de Medicina, Universidad Católica del Maule, Talca, ChileLaboratorio de Fenómica y Embriogénesis Temprana (LAFET), Departamento de Biología Celular, Facultad de Ciencias Biológicas, Universidad de Concepción, Concepción, ChileFertilization is a critical process in sexual reproduction that involves the fusion of a capacitated sperm with a mature oocyte to form a zygote. Polyspermy, the fertilization of an oocyte by multiple sperm, leads to polyploidy and embryo lethality. Mammalian and non-mammalian oocytes have evolved mechanisms to prevent polyspermy, including fast and slow blocks. The fast block comprises membrane depolarization post-sperm fusion, temporarily preventing additional sperm fusion. The slow block, triggered by cortical granule (CG) exocytosis, involves the release of proteins that modify the zona pellucida to form a permanent barrier, avoiding the fertilization by additional sperm. The evidence shows that immature oocytes often fail to prevent polyspermy due to ineffective CG exocytosis, attributed to impaired intracellular calcium increases, lower content of this ion, and incomplete CG migration. The study of how genetic variations lead to observable phenotypes (phenogenetics) during the oocyte-to-embryo transition, have identified several maternal-effect genes in zebrafish involved in CG behavior. These genes regulate various stages of CG biology, including biosynthesis, maturation, and exocytosis. Mutations in these genes disrupt these processes, highlighting the maternal genetic control over CG properties. Zebrafish has emerged as a pivotal model for understanding the evolving genetic regulation and molecular mechanisms underlying CG biology, providing valuable insights into fertility and early embryonic development.https://www.frontiersin.org/articles/10.3389/fcell.2025.1514461/fullfertilizationzebrafishcortical granule dynamicsoocyte maturationpolyspermy
spellingShingle Priscila García-Castro
Isabella Giambó-Falian
Ingrid Carvacho
Ricardo Fuentes
Phenogenetics of cortical granule dynamics during zebrafish oocyte-to-embryo transition
Frontiers in Cell and Developmental Biology
fertilization
zebrafish
cortical granule dynamics
oocyte maturation
polyspermy
title Phenogenetics of cortical granule dynamics during zebrafish oocyte-to-embryo transition
title_full Phenogenetics of cortical granule dynamics during zebrafish oocyte-to-embryo transition
title_fullStr Phenogenetics of cortical granule dynamics during zebrafish oocyte-to-embryo transition
title_full_unstemmed Phenogenetics of cortical granule dynamics during zebrafish oocyte-to-embryo transition
title_short Phenogenetics of cortical granule dynamics during zebrafish oocyte-to-embryo transition
title_sort phenogenetics of cortical granule dynamics during zebrafish oocyte to embryo transition
topic fertilization
zebrafish
cortical granule dynamics
oocyte maturation
polyspermy
url https://www.frontiersin.org/articles/10.3389/fcell.2025.1514461/full
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AT isabellagiambofalian phenogeneticsofcorticalgranuledynamicsduringzebrafishoocytetoembryotransition
AT ingridcarvacho phenogeneticsofcorticalgranuledynamicsduringzebrafishoocytetoembryotransition
AT ricardofuentes phenogeneticsofcorticalgranuledynamicsduringzebrafishoocytetoembryotransition