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Updated: Sep 19, 2025

Meiotic Spindle Assessment in Mouse Oocytes by siRNA-mediated Silencing
Published on: October 11, 2015
MPS1 promotes timely spindle bipolarization to prevent kinetochore-microtubule attachment errors in oocytes
Shuhei Yoshida1, Reiko Nakagawa2, Kohei Asai3,4
1Laboratory for Chromosome Segregation, RIKEN Center for Biosystems Dynamics Research (BDR), Kobe, Japan. shuhei.yoshida@riken.jp.
Abstract:
Incorrect kinetochore-microtubule attachment leads to chromosome segregation errors. The risk of incorrect attachment is high in acentrosomal oocytes, where kinetochores are surrounded by randomly oriented microtubules until spindle bipolarization. Regulation of the temporal relationship between acentrosomal spindle bipolarization and kinetochore-microtubule attachment is unknown. Here, we show that in mouse oocytes, MPS1, a kinase more active at kinetochores with less stable microtubule attachment, promotes timely spindle bipolarization before kinetochores stably attach to microtubules. In MPS1-inhibited oocytes, spindle bipolarization is delayed and depends on microtubules stably attached to kinetochores, resulting in incorrect attachments. We propose a two-step kinetochore-based model where unstable and stable attachment states act sequentially for acentrosomal spindle assembly to reduce the risk of egg aneuploidy.
Insights
Mitotic Centrosome Protein 1 (MPS1) kinase ensures correct chromosome segregation in mouse oocytes by promoting timely spindle bipolarization before stable kinetochore-microtubule attachment, preventing aneuploidy.
Area of Science:
- Cell Biology
- Molecular Biology
- Genetics
Background:
- Incorrect kinetochore-microtubule attachment causes chromosome segregation errors.
- Acentrosomal oocytes face high risk due to random microtubule orientation before spindle bipolarization.
Purpose of the Study:
- Investigate the regulation of spindle bipolarization and kinetochore-microtubule attachment timing in acentrosomal oocytes.
- Determine the role of MPS1 kinase in this process.
Main Methods:
- Utilized mouse oocytes.
- Investigated the function of MPS1 kinase through inhibition experiments.
- Observed kinetochore-microtubule attachment and spindle bipolarization dynamics.
Main Results:
- MPS1 kinase promotes timely spindle bipolarization before stable kinetochore-microtubule attachment.
- Inhibition of MPS1 delays spindle bipolarization, making it dependent on stable attachments.
- Delayed bipolarization leads to incorrect kinetochore-microtubule attachments.
Conclusions:
- Propose a two-step kinetochore-based model for acentrosomal spindle assembly.
- Unstable and stable microtubule attachment states sequentially regulate spindle formation.
- This mechanism reduces the risk of egg aneuploidy.
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