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Updated: Sep 20, 2026

Use of Time-Lapse Microscopy and Stage-Specific Nuclear Depletion of Proteins to Study Meiosis in S. cerevisiae
Published on: October 11, 2022
Cyclin-dependent kinase 2 is essential for meiosis but not for mitotic cell division in mice
Sagrario Ortega1, Ignacio Prieto, Junko Odajima
1Molecular Oncology Program, Centro Nacional de Investigaciones Oncológicas, Melchor Fernández Almagro 3, Madrid E-28029, Spain. sortega@cnio.es
Abstract:
We targeted the locus encoding the cyclin-dependent kinase 2 (CDK2) by homologous recombination in mouse embryonic stem (ES) cells. Embryonic fibroblasts lacking CDK2 proliferate normally and become immortal after continuous passage in culture. Elimination of a conditional Cdk2 allele in immortal cells does not have a significant effect on proliferation. Cdk2-/- mice are viable and survive for up to two years, indicating that CDK2 is also dispensable for proliferation and survival of most cell types. But CDK2 is essential for completion of prophase I during meiotic cell division in male and female germ cells, an unforeseen role for this cell cycle kinase.
Insights
Cyclin-dependent kinase 2 (CDK2) is dispensable for normal cell proliferation and survival in mice. However, CDK2 plays a critical role in completing meiosis, specifically prophase I, in germ cells.
Area of Science:
- Molecular Biology
- Cell Biology
- Genetics
Background:
- Cyclin-dependent kinase 2 (CDK2) is a key regulator of the cell cycle.
- Its precise role in organismal development and cell proliferation requires further investigation.
Purpose of the Study:
- To investigate the in vivo function of CDK2.
- To determine the necessity of CDK2 for cell proliferation and organismal survival.
Main Methods:
- Homologous recombination was used to generate Cdk2 knockout mouse embryonic stem cells.
- Phenotypic analysis of Cdk2-deficient mice and fibroblasts was performed.
- Assessment of meiotic progression in germ cells was conducted.
Main Results:
- Cdk2 knockout mice are viable and survive for up to two years.
- Embryonic fibroblasts lacking CDK2 proliferate normally and can become immortalized.
- CDK2 is essential for the completion of prophase I during male and female meiosis.
Conclusions:
- CDK2 is dispensable for the proliferation and survival of most somatic cells.
- CDK2 has an essential, previously unrecognized role in meiotic cell division.
- This study reveals a critical function of CDK2 in gametogenesis.
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