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Updated: Aug 11, 2026

Detection of DNA Double-Stranded Breaks in Mouse Oocytes
Published on: June 23, 2023
TRIM28 regulate G2/M transition via histone modification and DNA damage repair during mouse oocyte meiosis
Rui-Jie Ma1, Meng-Meng Tang1, Ping-Shuang Lu1
1College of Animal Science and Technology, Nanjing Agricultural University, Nanjing 210095, China.
Abstract:
TRIM28, a member of the tripartite motif (TRIM) family, functions as a transcriptional coregulator involved in maintaining genome stability during mitosis. However, transcriptional activity is barely detectable during oocyte meiotic maturation. In this study, we explored the role of TRIM28 in mouse oocytes and found that it was constitutively expressed in the early stages of oocyte meiotic maturation, with predominant nuclear localization in germinal vesicle (GV)-stage oocytes. TRIM28 depletion caused defective germinal vesicle breakdown (GVBD), but oocytes that successfully underwent GVBD displayed unimpaired first polar body (PB1) extrusion. TRIM28 depletion impaired CDK1 activity and reduced cyclin B1 levels, leading to a delay in the G2/M transition. This delay may be attributed to altered levels of HDAC2-mediated H4K12ac and H3K4me2-modulated H3K9me2 in nonsurrounded nucleolus (NSN)-type GV oocytes, which decreased transcription activity. Additionally, TRIM28-depleted oocytes exhibited elevated γ-H2A.X expression, accompanied by aberrant expression of CHK1 and CHK2, as well as dysregulated expression of RAD51, which were collectively contributed to GVBD failure in mouse oocytes. In conclusion, our findings indicate that TRIM28 participates in the regulation of the G2/M transition during mouse oocyte meiotic maturation, acting through the modulation of histone modifications and DNA damage repair.
Insights
Tripartite motif 28 (TRIM28) is crucial for mouse oocyte meiotic maturation, regulating the G2/M transition. Its depletion causes DNA damage and delays maturation by affecting histone modifications and DNA repair pathways.
Area of Science:
- Cell Biology
- Molecular Biology
- Genetics
Background:
- Tripartite motif 28 (TRIM28) is a transcriptional coregulator essential for genome stability during mitosis.
- Its role during oocyte meiotic maturation, a period of low transcriptional activity, remains largely unexplored.
Purpose of the Study:
- To investigate the function of TRIM28 in mouse oocyte meiotic maturation.
- To elucidate the molecular mechanisms underlying TRIM28's role in regulating the G2/M transition and genome stability.
Main Methods:
- TRIM28 depletion using RNA interference in mouse oocytes.
- Analysis of meiotic progression, germinal vesicle breakdown (GVBD), and first polar body (PB1) extrusion.
- Assessment of cell cycle regulators (CDK1, cyclin B1), histone modifications (H4K12ac, H3K9me2), and DNA damage markers (γ-H2A.X, CHK1/2, RAD51).
Main Results:
- TRIM28 is constitutively expressed and localized to the nucleus in germinal vesicle (GV)-stage oocytes.
- TRIM28 depletion caused delayed G2/M transition, impaired GVBD, but not PB1 extrusion.
- Depletion affected CDK1 activity, cyclin B1 levels, histone modifications, and increased DNA damage signaling, leading to GVBD failure.
Conclusions:
- TRIM28 plays a critical role in regulating the G2/M transition during mouse oocyte meiotic maturation.
- TRIM28 modulates histone modifications and DNA damage repair pathways to ensure proper meiotic progression.
- TRIM28 is essential for maintaining genome stability and successful meiotic maturation in oocytes.
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