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Updated: Nov 3, 2025

Using Mouse Oocytes to Assess Human Gene Function During Meiosis I
Published on: April 10, 2018
Ribonucleic Acid Export 1 Is a Kinetochore-Associated Protein That Participates in Chromosome Alignment in Mouse
Fan Chen1, Xiao-Fei Jiao1, Fei Meng1
1Key Laboratory of Agricultural Animal Genetics, Breeding and Reproduction of Ministry of Education, College of Animal Science and Technology, Huazhong Agricultural University, Wuhan 430070, China.
Abstract:
Ribonucleic acid export 1 (Rae1) is an important nucleoporin that participates in mRNA export during the interphase of higher eukaryotes and regulates the mitotic cell cycle. In this study, small RNA interference technology was used to knockdown Rae1, and immunofluorescence, immunoblotting, and chromosome spreading were used to study the role of Rae1 in mouse oocyte meiotic maturation. We found that Rae1 is a crucial regulator of meiotic maturation of mouse oocytes. After the resumption of meiosis (GVBD), Rae1 was concentrated on the kinetochore structure. The knockdown of Rae1 by a specific siRNA inhibited GVBD progression at 2 h, finally leading to a decreased 14 h polar body extrusion (PBE) rate. However, a comparable 14 h PBE rate was found in the control, and the Rae1 knockdown groups that had already undergone GVBD. Furthermore, we found elevated PBE after 9.5 h in the Rae1 knockdown oocytes. Further analysis revealed that Rae1 depletion significantly decreased the protein level of securin. In addition, we detected weakened kinetochore-microtubule (K-MT) attachments, misaligned chromosomes, and an increased incidence of aneuploidy in the Rae1 knockdown oocytes. Collectively, we propose that Rae1 modulates securin protein levels, which contribute to chromosome alignment, K-MT attachments, and aneuploidy in meiosis.
Insights
Ribonucleic acid export 1 (Rae1) is vital for mouse oocyte maturation, regulating cell cycle progression and chromosome alignment. Rae1 depletion impairs meiosis, leading to aneuploidy, but does not affect polar body extrusion rates in later stages.
Area of Science:
- Cell Biology
- Developmental Biology
- Genetics
Background:
- Ribonucleic acid export 1 (Rae1) is a key nucleoporin involved in mRNA export and mitotic cell cycle regulation in eukaryotes.
- Its role in female meiosis, particularly in mammalian oocytes, remains incompletely understood.
Purpose of the Study:
- To investigate the function of Rae1 in mouse oocyte meiotic maturation.
- To elucidate the molecular mechanisms by which Rae1 influences meiotic progression and chromosome integrity.
Main Methods:
- Small interfering RNA (siRNA) technology was employed to knockdown Rae1 expression in mouse oocytes.
- Immunofluorescence, immunoblotting, and chromosome spreading techniques were utilized to assess meiotic progression, protein levels, and chromosome status.
Main Results:
- Rae1 knockdown inhibited germinal vesicle breakdown (GVBD) progression and affected polar body extrusion (PBE) rates.
- Rae1 depletion led to decreased securin protein levels, weakened kinetochore-microtubule (K-MT) attachments, chromosome misalignment, and increased aneuploidy.
- Elevated PBE was observed in Rae1-depleted oocytes after 9.5 hours.
Conclusions:
- Rae1 is a crucial regulator of mouse oocyte meiotic maturation, impacting GVBD, chromosome alignment, and segregation.
- Rae1 modulates securin protein levels, which are critical for proper K-MT attachments and preventing aneuploidy during meiosis.
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