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Updated: Feb 10, 2026

Using Mouse Oocytes to Assess Human Gene Function During Meiosis I
Published on: April 10, 2018
Maturation-promoting factor governs mitogen-activated protein kinase activation and interphase suppression during
Liat Ben-Yehoshua Josefsberg1, Dalia Galiani, Shlomi Lazar
1Department of Biological Regulation, The Weizmann Institute of Science, Rehovot 76100, Israel.
Abstract:
Meiosis is a particular example of a cell cycle, characterized by two successive divisions without an intervening interphase. Resumption of meiosis in oocytes is associated with activation of maturation-promoting factor (MPF) and mitogen-activated protein kinase (MAPK). The activity of MPF declines during the transition between the two meiotic divisions, whereas the activity of MAPK is sustained. Attempts to disclose the interplay between these key regulators of meiosis in both amphibian and mammalian oocytes generated contradictory results. Furthermore, the enzyme that governs the suppression of interphase in mammals is still unidentified. To our knowledge, we provide herein the first demonstration in a mammalian system that inhibition of MPF at reinitiation of meiosis abrogated Mos expression and MAPK activation. We also show that oocytes, in which reactivation of MPF at completion of the first telophase was prevented, exhibited an interphase nucleus with decondensed chromosomes. Inhibition of MAPK did not interfere with the progression to the second meiotic metaphase but, rather, resulted in parthenogenic activation. We conclude that in rat oocytes, MPF regulates MAPK activation and its timely reactivation prevents the oocytes from entering interphase.
Insights
Maturation-promoting factor (MPF) regulates mitogen-activated protein kinase (MAPK) activation during meiosis resumption in rat oocytes. Timely MPF reactivation prevents oocytes from entering interphase, ensuring proper meiotic progression.
Area of Science:
- Cell Biology
- Developmental Biology
- Reproductive Biology
Background:
- Meiosis involves two divisions without interphase, regulated by maturation-promoting factor (MPF) and mitogen-activated protein kinase (MAPK).
- The interplay between MPF and MAPK during oocyte meiosis resumption is not fully understood, particularly the mechanism suppressing interphase in mammals.
- Previous studies on amphibian and mammalian oocytes yielded conflicting results regarding these regulators.
Purpose of the Study:
- To elucidate the role of MPF in regulating MAPK activation during meiosis resumption in mammalian oocytes.
- To identify the mechanism that suppresses interphase during meiosis in mammalian oocytes.
- To investigate the consequences of MPF and MAPK inhibition on meiotic progression and activation.
Main Methods:
- Utilized rat oocytes as a mammalian model system.
- Manipulated MPF activity at key stages of meiosis reinitiation and progression.
- Assessed Mos expression, MAPK activation, chromosome condensation, and nuclear status.
- Inhibited MAPK activity to observe its effect on meiotic progression.
Main Results:
- Inhibition of MPF at meiosis reinitiation blocked Mos expression and MAPK activation.
- Preventing MPF reactivation after the first meiotic division led to interphase nucleus formation with decondensed chromosomes.
- MAPK inhibition did not impede progression to the second meiotic metaphase but induced parthenogenic activation.
- Demonstrated that MPF regulates MAPK activation in rat oocytes.
Conclusions:
- MPF plays a crucial role in initiating MAPK activation during meiosis resumption in rat oocytes.
- Timely reactivation of MPF is essential for preventing the entry of oocytes into interphase.
- These findings clarify the regulatory roles of MPF and MAPK in mammalian oocyte meiosis and interphase suppression.
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