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The cyclic behavior of a cytoplasmic factor controlling nuclear membrane breakdown
The Journal of Cell Biology
|July 1, 1978
Summary
Maturation-promoting factor (MPF) drives nuclear envelope breakdown in amphibian oocytes and embryos. Its activity cycles during early development, peaking at mitosis, and requires protein synthesis for reappearance.
Area of Science:
- Cell Biology
- Developmental Biology
- Molecular Biology
Background:
- Cytoplasmic factors regulate key cell cycle events.
- Maturation-promoting factor (MPF) induces germinal vesicle breakdown in oocytes.
- Early embryonic development involves complex regulatory mechanisms.
Purpose of the Study:
- To investigate the role and regulation of MPF during early amphibian embryonic cleavage.
- To determine if MPF activity cycles during mitosis in embryos.
- To explore the cytoplasmic control over MPF activity.
Main Methods:
- Injection of cytoplasmic factors into amphibian oocytes.
- Monitoring MPF activity during early embryonic development.
- Analysis of MPF activity in enucleated and colchicine-arrested embryos.
- Assessment of protein synthesis requirement for MPF activity.
Main Results:
- MPF activity is high in mature oocytes but lost upon fertilization.
- MPF activity reappears and cycles during early cleavage, peaking at mitosis.
- MPF activity remains elevated and non-oscillating in colchicine-arrested embryos.
- Cytoplasmic control over MPF timing is demonstrated in enucleated eggs.
- Protein synthesis is necessary for MPF reappearance but not its disappearance.
Conclusions:
- MPF plays a crucial role in nuclear membrane breakdown during both meiosis and mitosis.
- MPF activity is regulated cyclically during early embryonic development.
- Cytoplasmic factors and protein synthesis are key regulators of MPF activity in embryos.