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Updated: May 29, 2026

Meiotic Spindle Assessment in Mouse Oocytes by siRNA-mediated Silencing
Published on: October 11, 2015
Serum- and Glucocorticoid-Regulated Kinase 1 Regulates Spindle Assembly Through RanBP1 During Oocyte Meiosis
Li-Shu Li1, Shu-Jie Yang2, Xiao-Qing Li2
1Key Laboratory of Environmental Medicine Engineering, Ministry of Education, School of Public Health, Southeast University, Nanjing, Jiangsu, China.
Abstract:
Advanced maternal age is associated with increased oocyte aneuploidy and early miscarriage. Serum- and glucocorticoid-regulated kinase 1 (SGK1), a member of the serine/threonine kinase family, is downregulated in oocytes from aged mice. However, the mechanisms by which SGK1 controls oocyte maturation remain unclear. Here, we show that SGK1 localizes predominantly to spindle poles during oocyte maturation. Knockdown of SGK1 via siRNA or pharmacological inhibition disrupts spindle assembly and impairs kinetochore-microtubule attachments in mouse oocytes. This disruption leads to sustained activation of the spindle assembly checkpoint, failure of Cyclin B1 and Securin degradation, impaired metaphase I-anaphase transition, and defective first polar body extrusion. Mechanistically, we identify RanBP1 as a potential mediator of SGK1 function during meiotic progression. In porcine oocytes, SGK1 inhibition similarly compromises maturation and Cyclin B1 degradation, suggesting a conserved role across mammalian species. Together, our findings establish SGK1 as a critical regulator of spindle assembly and meiotic progression in mammalian oocytes.
Insights
Serum- and glucocorticoid-regulated kinase 1 (SGK1) is crucial for mammalian oocyte maturation. Its downregulation impairs spindle assembly and meiotic progression, potentially contributing to age-related infertility.
Area of Science:
- Reproductive Biology
- Cell Biology
- Molecular Genetics
Background:
- Advanced maternal age correlates with increased oocyte aneuploidy and miscarriage.
- Serum- and glucocorticoid-regulated kinase 1 (SGK1) is downregulated in oocytes from aged mice, but its role in maturation is unknown.
Purpose of the Study:
- To elucidate the mechanisms by which SGK1 regulates oocyte maturation and meiotic progression.
Main Methods:
- SGK1 localization studies in mouse oocytes.
- SGK1 knockdown using siRNA and pharmacological inhibition.
- Analysis of spindle assembly, kinetochore-microtubule attachments, and meiotic progression.
- Investigation of potential mediators like RanBP1.
- Comparative studies in porcine oocytes.
Main Results:
- SGK1 localizes to spindle poles during oocyte maturation.
- SGK1 inhibition disrupts spindle assembly and kinetochore-microtubule attachments.
- This leads to spindle assembly checkpoint activation, failed degradation of Cyclin B1 and Securin, and impaired meiotic transition.
- RanBP1 is identified as a potential SGK1 mediator.
- Similar defects observed in porcine oocytes, indicating conserved function.
Conclusions:
- SGK1 is essential for proper spindle assembly and meiotic progression in mammalian oocytes.
- Dysregulation of SGK1 may contribute to infertility associated with advanced maternal age.
- SGK1's role in oocyte maturation is conserved across mammalian species.
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