Literature DB >> 9539747

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

J Iwashita1, Y Hayano, N Sagata.   

Abstract

In almost all animal species, immature oocytes are arrested naturally in the first meiotic prophase, with a large nucleus called the germinal vesicle. A number of previous studies showed that both activation of maturation/M phase-promoting factor (MPF) (assayed by semiquantitative cytological methods) and some other maturational events occur essentially normally in enucleated oocytes from many amphibian species and mice. Hence, for nearly three decades, it has generally been believed that nuclear material is dispensable for MPF activation and the meiotic cell cycle in vertebrate oocytes. Here, we have challenged this view by examining the histone H1 kinase activities and the molecular forms of MPF in experimentally manipulated Xenopus oocytes. We show that oocytes injected with nuclear material undergo much more rapid MPF activation and maturation than uninjected control oocytes. Conversely, enucleated oocytes, unlike nucleated counterparts, undergo only weak MPF activation in meiosis I and no detectable MPF reactivation in meiosis II, the latter accompanying inhibitory tyrosine phosphorylation of cdc2 kinase, the catalytic subunit of MPF. These results argue strongly that nuclear material is indispensable for the meiotic cell cycle, particularly MPF reactivation (or cdc2 tyrosine dephosphorylation) on entry into meiosis II, in Xenopus oocytes. The classical and general view may thus need reconsideration.

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Year:  1998        PMID: 9539747      PMCID: PMC22499          DOI: 10.1073/pnas.95.8.4392

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  39 in total

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Journal:  Dev Biol       Date:  1976-05       Impact factor: 3.582

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Journal:  Exp Cell Res       Date:  1969-04       Impact factor: 3.905

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Journal:  Cell       Date:  1988-02-26       Impact factor: 41.582

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Journal:  Dev Biol       Date:  1988-07       Impact factor: 3.582

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Journal:  Exp Cell Res       Date:  1980-07       Impact factor: 3.905

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Journal:  Dev Biol       Date:  1981-01-15       Impact factor: 3.582

Review 8.  Local control mechanisms during oogenesis and folliculogenesis.

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Journal:  Dev Biol (N Y 1985)       Date:  1985

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Journal:  J Cell Biol       Date:  1976-03       Impact factor: 10.539

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Journal:  J Cell Biol       Date:  1984-04       Impact factor: 10.539

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  6 in total

1.  Identification of XPR-1, a progesterone receptor required for Xenopus oocyte activation.

Authors:  J Tian; S Kim; E Heilig; J V Ruderman
Journal:  Proc Natl Acad Sci U S A       Date:  2000-12-19       Impact factor: 11.205

2.  Pre-M phase-promoting factor associates with annulate lamellae in Xenopus oocytes and egg extracts.

Authors:  Clare Beckhelling; Patrick Chang; Sandra Chevalier; Chris Ford; Evelyn Houliston
Journal:  Mol Biol Cell       Date:  2003-03       Impact factor: 4.138

3.  MPF localization is controlled by nuclear export.

Authors:  A Hagting; C Karlsson; P Clute; M Jackman; J Pines
Journal:  EMBO J       Date:  1998-07-15       Impact factor: 11.598

4.  Nuclei and microtubule asters stimulate maturation/M phase promoting factor (MPF) activation in Xenopus eggs and egg cytoplasmic extracts.

Authors:  D Pérez-Mongiovi; C Beckhelling; P Chang; C C Ford; E Houliston
Journal:  J Cell Biol       Date:  2000-09-04       Impact factor: 10.539

Review 5.  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

6.  Greatwall kinase and cyclin B-Cdk1 are both critical constituents of M-phase-promoting factor.

Authors:  Masatoshi Hara; Yusuke Abe; Toshiaki Tanaka; Takayoshi Yamamoto; Eiichi Okumura; Takeo Kishimoto
Journal:  Nat Commun       Date:  2012       Impact factor: 14.919

  6 in total

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