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Relocation and distinct subcellular localization of p34cdc2-cyclin B complex at meiosis reinitiation in starfish

K Ookata1, S Hisanaga, T Okano

  • 1Department of Biological Science, Tokyo Institute of Technology, Yokohama, Japan.

The EMBO Journal
|May 1, 1992
PubMed

Insights

M phase promoting factor (MPF), composed of p34cdc2 and cyclin B, controls cell cycle entry. Its relocation within starfish oocytes is crucial for M phase promotion.

Area of Science:

  • Cell Biology
  • Molecular Biology
  • Developmental Biology

Background:

  • M phase promoting factor (MPF) regulates eukaryotic cell cycle entry.
  • MPF comprises p34cdc2 and cyclin B subunits.

Purpose of the Study:

  • To investigate the subcellular distribution dynamics of MPF during meiosis reinitiation in starfish oocytes.
  • To understand the role of MPF intracellular relocation in M phase promotion.

Main Methods:

  • Indirect immunofluorescence staining using a specific antibody against starfish cyclin B.
  • Monitoring subcellular localization of the p34cdc2-cyclin B complex in starfish oocytes.

Main Results:

  • Inactive p34cdc2-cyclin B complex is exclusively cytoplasmic in immature oocytes.
  • Activated MPF relocates to the germinal vesicle, nucleolus, chromosomes, meiotic asters, and spindles.
  • MPF localization occurs independently of microtubules or actin filaments.
  • Four distinct subcellular states of MPF were identified: soluble, microtubule-associated, cytoskeleton-associated, and chromosome-associated.

Conclusions:

  • Intracellular relocation of MPF is a key mechanism promoting M phase entry.
  • MPF's subcellular distribution is critical for regulating meiosis reinitiation.

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