Literature DB >> 9008413

What does Mos do in oocytes and somatic cells?

N Sagata1.   

Abstract

Mos, a protein kinase, is specifically expressed and functions during meiotic maturation (or G2/M progression) of vertebrate oocytes. When expressed ectopically, however, it can also readily induce oncogenic transformation (or uncontrolled G1/S transitions) in somatic cells. In both of these cell types, Mos activates mitogen-activated protein kinase (MAPK), which seems largely to mediate its different functions in both oocyte maturation and cellular transformation. In oocyte maturation, the Mos-MAPK pathway probably serves to activate and stabilize M-phase promoting factor (MPF) (possibly by inhibiting some negative regulator(s) of this factor), while in cellular transformation, it seems to stabilize and activate the nuclear oncoprotein c-Fos as well as to induce transcription of its gene. Thus, the different functions of Mos in oocytes and somatic cells may arise chiefly from its different MAPK-mediated targets in the respective cell types. This review discusses the cellular basis that may enable Mos to act differently in oocytes and somatic cells.

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Year:  1997        PMID: 9008413     DOI: 10.1002/bies.950190105

Source DB:  PubMed          Journal:  Bioessays        ISSN: 0265-9247            Impact factor:   4.345


  53 in total

1.  Absence of Wee1 ensures the meiotic cell cycle in Xenopus oocytes.

Authors:  N Nakajo; S Yoshitome; J Iwashita; M Iida; K Uto; S Ueno; K Okamoto; N Sagata
Journal:  Genes Dev       Date:  2000-02-01       Impact factor: 11.361

2.  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

Review 3.  Cytoplasmic polyadenylation in development and beyond.

Authors:  J D Richter
Journal:  Microbiol Mol Biol Rev       Date:  1999-06       Impact factor: 11.056

4.  The Mos pathway regulates cytoplasmic polyadenylation in Xenopus oocytes.

Authors:  C H de Moor; J D Richter
Journal:  Mol Cell Biol       Date:  1997-11       Impact factor: 4.272

5.  Mechanism of degradation of CPEB during Xenopus oocyte maturation.

Authors:  Daiki Setoyama; Masakane Yamashita; Noriyuki Sagata
Journal:  Proc Natl Acad Sci U S A       Date:  2007-11-06       Impact factor: 11.205

6.  Aurora A, mitotic entry, and spindle bipolarity.

Authors:  Quentin Liu; Joan V Ruderman
Journal:  Proc Natl Acad Sci U S A       Date:  2006-03-31       Impact factor: 11.205

7.  The C.elegans MAPK phosphatase LIP-1 is required for the G(2)/M meiotic arrest of developing oocytes.

Authors:  Alex Hajnal; Thomas Berset
Journal:  EMBO J       Date:  2002-08-15       Impact factor: 11.598

8.  A conserved E2F6-binding element in murine meiosis-specific gene promoters.

Authors:  Sarah M Kehoe; Masahiro Oka; Katherine E Hankowski; Nina Reichert; Sandra Garcia; John R McCarrey; Stefan Gaubatz; Naohiro Terada
Journal:  Biol Reprod       Date:  2008-07-30       Impact factor: 4.285

9.  Cap ribose methylation of c-mos mRNA stimulates translation and oocyte maturation in Xenopus laevis.

Authors:  H Kuge; G G Brownlee; P D Gershon; J D Richter
Journal:  Nucleic Acids Res       Date:  1998-07-01       Impact factor: 16.971

10.  Phosphorylation of high-mobility group protein A2 by Nek2 kinase during the first meiotic division in mouse spermatocytes.

Authors:  Silvia Di Agostino; Monica Fedele; Paolo Chieffi; Alfredo Fusco; Pellegrino Rossi; Raffaele Geremia; Claudio Sette
Journal:  Mol Biol Cell       Date:  2003-12-10       Impact factor: 4.138

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