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Updated: Nov 15, 2025

Using Mouse Oocytes to Assess Human Gene Function During Meiosis I
Published on: April 10, 2018
Stable kinetochore-microtubule attachments restrict MTOC position and spindle elongation in oocytes
Aurélien Courtois1, Shuhei Yoshida1, Osamu Takenouchi1
1Laboratory for Chromosome Segregation, RIKEN Center for Biosystems Dynamics Research (BDR), Kobe, Japan.
Abstract:
In mouse oocytes, acentriolar MTOCs functionally replace centrosomes and act as microtubule nucleation sites. Microtubules nucleated from MTOCs initially assemble into an unorganized ball-like structure, which then transforms into a bipolar spindle carrying MTOCs at its poles, a process called spindle bipolarization. In mouse oocytes, spindle bipolarization is promoted by kinetochores but the mechanism by which kinetochore-microtubule attachments contribute to spindle bipolarity remains unclear. This study demonstrates that the stability of kinetochore-microtubule attachment is essential for confining MTOC positions at the spindle poles and for limiting spindle elongation. MTOC sorting is gradual and continues even in the metaphase spindle. When stable kinetochore-microtubule attachments are disrupted, the spindle is unable to restrict MTOCs at its poles and fails to terminate its elongation. Stable kinetochore fibers are directly connected to MTOCs and to the spindle poles. These findings suggest a role for stable kinetochore-microtubule attachments in fine-tuning acentrosomal spindle bipolarity.
Insights
Stable kinetochore-microtubule attachments are crucial for organizing microtubule organizing centers (MTOCs) during spindle bipolarization in mouse oocytes. Disrupting these attachments prevents proper spindle formation and elongation control.
Area of Science:
- Cell Biology
- Molecular Biology
- Developmental Biology
Background:
- Acentriolar microtubule organizing centers (MTOCs) in mouse oocytes replace centrosomes for microtubule nucleation.
- Spindle bipolarization, the formation of a bipolar spindle from nucleated microtubules, is essential for cell division.
- Kinetochores promote spindle bipolarization, but the precise role of kinetochore-microtubule attachments is not fully understood.
Purpose of the Study:
- To investigate the mechanism by which kinetochore-microtubule attachments contribute to spindle bipolarity in mouse oocytes.
- To determine the role of stable kinetochore-microtubule attachments in MTOC positioning and spindle elongation.
Main Methods:
- Live-cell imaging of microtubules and MTOCs in mouse oocytes.
- Perturbation of kinetochore-microtubule attachments using chemical inhibitors or genetic manipulation.
- Analysis of spindle morphology, MTOC localization, and spindle length.
Main Results:
- The stability of kinetochore-microtubule attachments is essential for confining MTOCs to spindle poles.
- Disruption of stable attachments leads to uncontrolled spindle elongation and failure to restrict MTOCs.
- MTOC sorting is a gradual process that persists into metaphase, regulated by stable kinetochore fibers.
Conclusions:
- Stable kinetochore-microtubule attachments play a critical role in regulating acentrosomal spindle bipolarity by controlling MTOC positioning and spindle length.
- These attachments act as crucial regulators, ensuring proper spindle organization and termination of elongation in the absence of centrosomes.
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