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Updated: Sep 9, 2025

Multi-Photon Laser Ablation of Cytoplasmic Microtubule Organizing Centers in Mouse Oocytes
Published on: November 11, 2022
The mechanisms of MTOCs maturation in human and mouse oocytes
Hao Gu1, Ling Wu2, Mingru Yin2
1Institute of Pediatrics, Children's Hospital of Fudan University, State Key Laboratory of Genetic Engineering, Institutes of Biomedical Sciences, Fudan University, Shanghai 200032, China.
Abstract:
The microtubule organizing centers (MTOCs) of human and mouse oocytes are essential for meiotic spindle assembly and for ensuring precise chromosome segregations. Previous studies mainly focus on investigating MTOCs changes in metaphase I oocyte. However, the detailed dynamic changes and underlying mechanisms of the MTOCs in germinal vesicle (GV) oocytes-a stage that early events of MTOC maturation happened- remain unclear. Here we explored the dynamics of MTOCs maturation in human and mouse GV oocytes and found that MTOCs maturation is a largely conserved process, consisting of two tightly coupled processes referred to as MTOCs activation and migration. We found that cytoskeleton associated protein 5 (CKAP5) and transforming acidic coiled-coil containing protein 3 (TACC3) play key roles in MTOCs maturation in oocytes. The activation of the MTOCs is a prerequisite for migration initiation, and the migration of the MTOCs is facilitated by dynein/dynactin in oocytes. The disruption of MTOC maturation resulted in spindle assembly failure. Importantly, impaired MTOCs maturation is associated with the physiological aging of oocytes. This study provides a comprehensive understanding of MTOCs dynamics in human and mouse oocytes.
Insights
Microtubule organizing centers (MTOCs) in oocytes mature through activation and migration, a conserved process involving CKAP5 and TACC3. Impaired maturation links to aging and spindle failure.
Area of Science:
- Cell Biology
- Reproductive Biology
- Oocyte Development
Background:
- Microtubule organizing centers (MTOCs) are crucial for meiotic spindle assembly and chromosome segregation in oocytes.
- Previous research primarily examined MTOCs in metaphase I, leaving dynamics in germinal vesicle (GV) oocytes understudied.
Purpose of the Study:
- To investigate the dynamic changes and underlying mechanisms of MTOC maturation in human and mouse GV oocytes.
- To elucidate the roles of specific proteins in MTOC maturation and its implications for oocyte quality.
Main Methods:
- Exploration of MTOC dynamics in human and mouse GV oocytes.
- Investigation of the involvement of cytoskeleton-associated protein 5 (CKAP5) and transforming acidic coiled-coil containing protein 3 (TACC3).
- Analysis of the roles of dynein/dynactin in MTOC migration.
Main Results:
- MTOC maturation is a conserved process in GV oocytes, involving activation and migration.
- CKAP5 and TACC3 are key players in oocyte MTOC maturation.
- MTOC activation precedes migration, which is facilitated by dynein/dynactin.
- Disruption of MTOC maturation leads to spindle assembly failure.
- Impaired MTOC maturation is associated with oocyte aging.
Conclusions:
- MTOC maturation in GV oocytes is a conserved, two-step process essential for reproductive success.
- CKAP5, TACC3, and dynein/dynactin are critical for MTOC dynamics and oocyte quality.
- Understanding MTOC maturation provides insights into oocyte aging and potential fertility issues.
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