Components of the signaling pathway linking the 1-methyladenine receptor to MPF activation and maturation in starfish oocytes

Kirsten C. Sadler, Joan V. Ruderman

Research output: Contribution to journalArticlepeer-review

Abstract

Starfish oocytes are arrested at the G2/M-phase border of meiosis I. Exposure to their natural mitogen, 1-methyladenine (1-MA), leads to the activation of MPF and MAP kinase, resumption of the meiotic cell cycle, and fertilization competency. The 1-MA receptor has not yet been identified, but it is known to be linked functionally to a pertussis toxin-sensitive G- protein. Gβγ appears to be the major effector of the 1-MA receptor, since injection of Gβγ, but not activated Gα(i), leads to the activation of MPF, entry into meiosis, and oocyte maturation. The components that connect Gβγ to MPF and MAP kinase activation in oocytes are unknown. In mammalian cells, a novel phosphatidylinositol 3-kinase, PI-3 kinase-γ, links Gβγ to the MAP kinase activation pathway. Here we show that PI-3 kinase is required for starfish oocyte maturation. LY294002 and wortmannin, inhibitors of PI-3 kinase, block MPF and MAP kinase activation and entry into meiosis. Inhibition by LY294002 is reversible and limited to the hormone-dependent period. Neither inhibitor, however, blocks the earliest hormone-induced event, formation of actin spikes at the cell membrane. By contrast, pertussis toxin blocks both actin spiking and later events, arguing that PI-3 kinase functions downstream of Gβγ. Finally, we show that unlike the well-studied case in Xenopus oocytes, where MAP kinase is an essential component of the MPF activation pathway, MAP kinase is not required for either MPF activation or subsequent oocyte maturation in starfish. Instead, its major role appears to be suppression of DNA synthesis in unfertilized, haploid eggs.

Original languageEnglish (US)
Pages (from-to)25-38
Number of pages14
JournalDevelopmental Biology
Volume197
Issue number1
DOIs
StatePublished - May 1 1998

ASJC Scopus subject areas

  • Molecular Biology
  • Developmental Biology
  • Cell Biology

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