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Updated: Aug 6, 2025

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Published on: June 6, 2017
Cell cycle regulation for meiosis in mammalian germ cells
Ryuki Shimada1, Kei-Ichiro Ishiguro1
1Department of Chromosome Biology, Institute of Molecular Embryology and Genetics (IMEG), Kumamoto University, Kumamoto 860-0811, Japan.
Abstract:
In mouse fetal gonads, germ cell development is accompanied by changes in cell cycle mode in response to external signals and intrinsic mechanisms of cells. During fetal development, male germ cells undergo G0/G1 arrest, while female germ cells exit the mitotic cell cycle and enter meiosis. In fetal testes, NANOS2 and CYP26B1 force germ cells to stay in G0/G1 arrest phase, preventing them from entering the meiotic cell cycle. In the fetal ovary, external signals, such as RA, BMP, and WNT, promote the competency of female germ cells to enter the meiotic cell cycle. MEIOSIN and STRA8 ensure the establishment of the meiotic cell cycle by activating meiotic genes, such that meiotic entry coincides with the S phase. This review discusses germ cell development from the viewpoint of cell cycle regulation and highlights the mechanism of the entry of germ cells into meiosis.
Insights
Germ cell development differs between sexes, with male germ cells arresting in G0/G1 phase and female germ cells entering meiosis. This review explores the cell cycle regulation mechanisms driving these distinct developmental pathways.
Area of Science:
- Reproductive Biology
- Developmental Biology
- Cell Cycle Regulation
Background:
- Germ cell development in fetal gonads is a complex process influenced by intrinsic and extrinsic factors.
- Male and female germ cells exhibit distinct cell cycle behaviors during fetal development: arrest in G0/G1 for males and entry into meiosis for females.
Approach:
- This review synthesizes current research on germ cell cycle regulation during fetal development.
- It examines the molecular mechanisms, including key genes and signaling pathways, that control germ cell fate in testes and ovaries.
Key Points:
- In fetal testes, NANOS2 and CYP26B1 maintain germ cell G0/G1 arrest, inhibiting entry into meiosis.
- In fetal ovaries, retinoic acid (RA), BMP, and WNT signaling promote meiotic entry competence.
- MEIOSIN and STRA8 are crucial for initiating the meiotic cell cycle in female germ cells, synchronizing meiotic entry with the S phase.
Conclusions:
- Cell cycle regulation is a critical determinant of sexual dimorphism in germ cell development.
- Understanding these mechanisms provides insight into the establishment of the germline and potential reproductive health issues.
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