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Updated: May 16, 2026

Meiotic Spindle Assessment in Mouse Oocytes by siRNA-mediated Silencing
Published on: October 11, 2015
WHAMM is required for meiotic spindle migration and asymmetric cytokinesis in mouse oocytes
1Organ Transplantation Institute, Xiamen University, Xiamen, Fujian, China.
Abstract:
WASP homolog associated with actin, membranes and microtubules (WHAMM) is a newly discovered nucleation-promoting factor that links actin and microtubule cytoskeleton and regulates transport from the endoplasmic reticulum to the Golgi apparatus. However, knowledge of WHAMM is limited to interphase somatic cells. In this study, we examined its localization and function in mouse oocytes during meiosis. Immunostaining showed that in the germinal vesicle (GV) stage, there was no WHAMM signal; after meiosis resumption, WHAMM was associated with the spindle at prometaphase I (Pro MI), metaphase I (MI), telophase I (TI) and metaphase II (MII) stages. Nocodazole and taxol treatments showed that WHAMM was localized around the MI spindle. Depletion of WHAMM by microinjection of specific short interfering (si)RNA into the oocyte cytoplasm resulted in failure of spindle migration, disruption of asymmetric cytokinesis and a decrease in the first polar body extrusion rate during meiotic maturation. Moreover, actin cap formation was also disrupted after WHAMM depletion, confirming the failure of spindle migration. Taken together, our data suggest that WHAMM is required for peripheral spindle migration and asymmetric cytokinesis during mouse oocyte maturation.
Insights
WASP homolog associated with actin, membranes and microtubules (WHAMM) is crucial for mouse oocyte maturation. It ensures proper spindle migration and asymmetric cytokinesis, vital for meiotic progression and polar body extrusion.
Area of Science:
- Cell Biology
- Reproductive Biology
- Cytoskeletal Dynamics
Background:
- WASP homolog associated with actin, membranes and microtubules (WHAMM) is a nucleation-promoting factor linking actin and microtubules.
- WHAMM's role is primarily studied in interphase somatic cells, with limited knowledge in meiosis.
Purpose of the Study:
- To investigate the localization and function of WHAMM in mouse oocytes during meiosis.
- To understand WHAMM's contribution to cytoskeletal organization and cell division in oocytes.
Main Methods:
- Immunostaining to determine WHAMM localization during different meiotic stages (GV, Pro MI, MI, TI, MII).
- Nocodazole and taxol treatments to analyze WHAMM association with the spindle.
- Short interfering (si)RNA microinjection to deplete WHAMM and observe functional consequences.
Main Results:
- WHAMM is not detected in the germinal vesicle (GV) stage but localizes to the spindle from prometaphase I to metaphase II.
- WHAMM depletion leads to failed spindle migration, disrupted asymmetric cytokinesis, and reduced first polar body extrusion.
- Actin cap formation is impaired upon WHAMM depletion, corroborating spindle migration failure.
Conclusions:
- WHAMM plays a critical role in regulating peripheral spindle migration during mouse oocyte maturation.
- WHAMM is essential for successful asymmetric cytokinesis and first polar body extrusion in oocytes.
- WHAMM integrates the actin and microtubule cytoskeleton to orchestrate key events in meiotic maturation.
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