Literature DB >> 2838346

The cell cycle can occur in starfish oocytes and embryos without the production of transferable MPF (maturation-promoting factor).

A Picard1, J C Labbe, M Doree.   

Abstract

All cells undergoing the transition from interphase to metaphase have been postulated to contain a "maturation-promoting factor" (MPF) capable of causing meiotic maturation when injected into immature oocytes. We have shown in an accompanying paper (A. Picard, M. C. Harricane, J. C. Labbe, and M. Doreé, 1988, Dev. Biol. 128, 121-128) that the basic oscillator driving the cell cycle still operates in maturing starfish oocytes and fertilized eggs in the absence of germinal vesicle (GV) material. Under such conditions of enucleation, we now show, however, that MPF activity cannot be detected after hormonal stimulation of prophase-arrested oocytes in Astropecten or after the normal time of second meiotic cleavage in Marthasterias. In contrast, cell cycles occur with the production of transferable MPF activity in embryos from which both pronuclei have been removed after fertilization. Reinjection of the entire contents of a GV after the normal time of second meiotic cleavage restores the ability of cytoplasm to induce meiotic maturation in immature recipient oocytes after transfer. Transduction of the hormonal stimulus at the level of the plasma membrane, stimulation of the phosphorylation of cytoplasmic proteins, and activation of a cycling Ca2+- and cyclic nucleotide-independent histone kinase still occur in the absence of GV material. Since previous studies have demonstrated that the presence of GV material in the recipient oocytes is absolutely required in starfish for the amplification of microinjected MPF (Kishimoto et al., 1981; Picard and Doree, 1984), we propose that some unidentified component of the GV is required, at least after the normal time of second meiotic cleavage in donor oocytes and at any time in recipient oocytes, for the successful transfer of MPF activity in starfish.

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Year:  1988        PMID: 2838346     DOI: 10.1016/0012-1606(88)90274-6

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  11 in total

1.  A nuclear factor required for specific translation of cyclin B may control the timing of first meiotic cleavage in starfish oocytes.

Authors:  S Galas; H Barakat; M Dorée; A Picard
Journal:  Mol Biol Cell       Date:  1993-12       Impact factor: 4.138

2.  Newly assembled cyclin B-cdc2 kinase is required to suppress DNA replication between meiosis I and meiosis II in starfish oocytes.

Authors:  A Picard; S Galas; G Peaucellier; M Dorée
Journal:  EMBO J       Date:  1996-07-15       Impact factor: 11.598

3.  Essential role of germinal vesicle material in the meiotic cell cycle of Xenopus oocytes.

Authors:  J Iwashita; Y Hayano; N Sagata
Journal:  Proc Natl Acad Sci U S A       Date:  1998-04-14       Impact factor: 11.205

4.  Mitogen-activated protein kinase activation down-regulates a mechanism that inactivates cyclin B-cdc2 kinase in G2-arrested oocytes.

Authors:  A Abrieu; M Dorée; A Picard
Journal:  Mol Biol Cell       Date:  1997-02       Impact factor: 4.138

5.  Elimination of cdc2 phosphorylation sites in the cdc25 phosphatase blocks initiation of M-phase.

Authors:  T Izumi; J L Maller
Journal:  Mol Biol Cell       Date:  1993-12       Impact factor: 4.138

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

Authors:  K Ookata; S Hisanaga; T Okano; K Tachibana; T Kishimoto
Journal:  EMBO J       Date:  1992-05       Impact factor: 11.598

Review 7.  Entry into mitosis: a solution to the decades-long enigma of MPF.

Authors:  Takeo Kishimoto
Journal:  Chromosoma       Date:  2015-02-25       Impact factor: 4.316

Review 8.  MPF-based meiotic cell cycle control: Half a century of lessons from starfish oocytes.

Authors:  Takeo Kishimoto
Journal:  Proc Jpn Acad Ser B Phys Biol Sci       Date:  2018       Impact factor: 3.493

9.  Initial triggering of M-phase in starfish oocytes: a possible novel component of maturation-promoting factor besides cdc2 kinase.

Authors:  E Okumura; T Sekiai; S Hisanaga; K Tachibana; T Kishimoto
Journal:  J Cell Biol       Date:  1996-01       Impact factor: 10.539

10.  Cyclin A potentiates maturation-promoting factor activation in the early Xenopus embryo via inhibition of the tyrosine kinase that phosphorylates cdc2.

Authors:  A Devault; D Fesquet; J C Cavadore; A M Garrigues; J C Labbé; T Lorca; A Picard; M Philippe; M Dorée
Journal:  J Cell Biol       Date:  1992-09       Impact factor: 10.539

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