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Updated: Sep 27, 2025

Preparation of Meiotic Chromosome Spreads from Mouse Oocytes for Assessment of Synapsis and Recombination
Published on: July 18, 2025
MAPRE2 regulates the first meiotic progression in mouse oocytes
Yuan-Yuan Li1, Wen-Long Lei1, Chang-Fa Zhang2
1State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, 100101, China.
Abstract:
Microtubule plus-end tracking proteins (+TIPs) associate with growing microtubule plus ends and control microtubule dynamics and interactions with different cellular structures during cell division, cell migration and morphogenesis. Microtubule-associated RP/EB family member 2 (MAPRE2/EB2) is a highly conserved core component of +TIPs networks, but whether this molecule is required for mammalian meiotic progression is unknown. In this study, we investigated the expression and function of MAPRE2 during oocyte maturation. Our results showed that MAPRE2 was consistently expressed from germinal vesicle (GV) to metaphase II (MII) stages and that MAPRE2 was distributed in the cytoplasm of oocytes at GV stage and along the spindle at metaphase I (MI) and MII stages. Small interfering RNA-mediated knockdown of Mapre2 severely impaired microtubule stability, kinetochore-microtubule attachment, and chromosome alignment and subsequently caused spindle assembly checkpoint (SAC) activation and cyclin B1 nondegradation, leading to failure of chromosome segregation and first polar body extrusion. This study demonstrates for the first time that MAPRE2 plays an important role during mouse oocyte meiosis.
Insights
Microtubule-associated RP/EB family member 2 (MAPRE2) is crucial for mouse oocyte maturation. Its depletion disrupts microtubule stability and chromosome alignment, leading to meiotic failure.
Area of Science:
- Cell Biology
- Developmental Biology
- Reproductive Biology
Background:
- Microtubule plus-end tracking proteins (+TIPs) regulate microtubule dynamics and cellular processes.
- MAPRE2 (EB2) is a core +TIP component, but its role in mammalian oocyte meiosis is uncharacterized.
Purpose of the Study:
- To investigate the expression and function of MAPRE2 during mouse oocyte maturation.
Main Methods:
- Quantitative analysis of MAPRE2 expression across oocyte maturation stages.
- Immunofluorescence microscopy to determine MAPRE2 localization.
- RNA interference (siRNA) to knockdown Mapre2 expression.
- Assessment of microtubule stability, kinetochore-microtubule attachments, chromosome alignment, spindle assembly checkpoint (SAC) activation, and cyclin B1 degradation.
Main Results:
- MAPRE2 is expressed throughout mouse oocyte maturation (GV to MII stages).
- MAPRE2 localizes to the cytoplasm in GV oocytes and along the spindle in MI and MII oocytes.
- Mapre2 knockdown severely impairs microtubule stability, kinetochore-microtubule attachment, and chromosome alignment.
- MAPRE2 depletion activates the SAC and inhibits cyclin B1 degradation, causing meiotic arrest and failure of chromosome segregation and polar body extrusion.
Conclusions:
- MAPRE2 is essential for proper microtubule organization and function during mouse oocyte meiosis.
- MAPRE2 plays a critical role in ensuring accurate chromosome segregation and successful completion of oocyte maturation.
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