Literature DB >> 1657664

c-mos proto-oncogene product is partly degraded after release from meiotic arrest and persists during interphase in mouse zygotes.

M Weber1, J Z Kubiak, R B Arlinghaus, J Pines, B Maro.   

Abstract

Recently, it has been shown that the product of the c-mos proto-oncogene is a component of cytostatic factor, an activity present in unfertilized eggs from vertebrates that arrests the cell cycle in metaphase of the second meiotic division (metaphase II) possibly by stabilizing maturation-promoting factor (MPF). We have studied the behavior of the c-mos product in metaphase II mouse oocytes and soon after activation. The amount of c-mos in the oocyte was still very high after second polar body extrusion, when cyclin B has been degraded and MPF activity had decreased dramatically. Degradation of c-mos takes place later, during the G1 phase of the first cell cycle and a residual amount of c-mos is detectable during the first zygotic interphase. Our data show that the degradation of c-mos is not involved in the release from the metaphase arrest.

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Year:  1991        PMID: 1657664     DOI: 10.1016/0012-1606(91)90347-6

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


  6 in total

1.  MAPK inactivation is required for the G2 to M-phase transition of the first mitotic cell cycle.

Authors:  A Abrieu; D Fisher; M N Simon; M Dorée; A Picard
Journal:  EMBO J       Date:  1997-11-03       Impact factor: 11.598

2.  Mos in the oocyte: how to use MAPK independently of growth factors and transcription to control meiotic divisions.

Authors:  Aude Dupré; Olivier Haccard; Catherine Jessus
Journal:  J Signal Transduct       Date:  2010-12-19

3.  F-actin mechanics control spindle centring in the mouse zygote.

Authors:  Agathe Chaigne; Clément Campillo; Raphaël Voituriez; Nir S Gov; Cécile Sykes; Marie-Hélène Verlhac; Marie-Emilie Terret
Journal:  Nat Commun       Date:  2016-01-04       Impact factor: 14.919

4.  The metaphase II arrest in mouse oocytes is controlled through microtubule-dependent destruction of cyclin B in the presence of CSF.

Authors:  J Z Kubiak; M Weber; H de Pennart; N J Winston; B Maro
Journal:  EMBO J       Date:  1993-10       Impact factor: 11.598

5.  Suppression of DNA replication via Mos function during meiotic divisions in Xenopus oocytes.

Authors:  N Furuno; M Nishizawa; K Okazaki; H Tanaka; J Iwashita; N Nakajo; Y Ogawa; N Sagata
Journal:  EMBO J       Date:  1994-05-15       Impact factor: 11.598

6.  The dynamics of MAPK inactivation at fertilization in mouse eggs.

Authors:  Jose Raul Gonzalez-Garcia; Josephine Bradley; Michail Nomikos; Laboni Paul; Zoltan Machaty; F Anthony Lai; Karl Swann
Journal:  J Cell Sci       Date:  2014-04-16       Impact factor: 5.285

  6 in total

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