Cdc2-cyclin B triggers H3 kinase activation of Aurora-A in Xenopus oocytes.

Abstract : Xenopus oocytes are arrested in meiotic prophase I and resume meiotic divisions in response to progesterone. Progesterone triggers activation of M-phase promoting factor (MPF) or Cdc2-cyclin B complex and neosynthesis of Mos kinase, responsible for MAPK activation. Both Cdc2 and MAPK activities are required for the success of meiotic maturation. However, the signaling pathway induced by progesterone and leading to MPF activation is poorly understood, and most of the targets of both Cdc2 and MAPK in the oocyte remain to be determined. Aurora-A is a Ser/Thr kinase involved in separation of centrosomes and in spindle assembly during mitosis. It has been proposed that in Xenopus oocytes Aurora-A could be an early component of the progesterone-transduction pathway, acting through the regulation of Mos synthesis upstream Cdc2 activation. We addressed here the question of Aurora-A regulation during meiotic maturation by using new in vitro and in vivo experimental approaches. We demonstrate that Cdc2 kinase activity is necessary and sufficient to trigger both Aurora-A phosphorylation and kinase activation in Xenopus oocyte. In contrast, these events are independent of the Mos/MAPK pathway. Aurora-A is phosphorylated in vivo at least on three residues that regulate differentially its kinase activity. Therefore, Aurora-A is under the control of Cdc2 in the Xenopus oocyte and could be involved in meiotic spindle establishment.
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Journal of Biological Chemistry, American Society for Biochemistry and Molecular Biology, 2003, 278 (24), pp.21439-49. 〈10.1074/jbc.M300811200〉
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Soumis le : mercredi 26 mars 2014 - 16:51:15
Dernière modification le : vendredi 31 août 2018 - 09:18:16

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Gilliane Maton, Catherine Thibier, Anna Castro, Thierry Lorca, Claude Prigent, et al.. Cdc2-cyclin B triggers H3 kinase activation of Aurora-A in Xenopus oocytes.. Journal of Biological Chemistry, American Society for Biochemistry and Molecular Biology, 2003, 278 (24), pp.21439-49. 〈10.1074/jbc.M300811200〉. 〈inserm-00966489〉

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