PDK1 is required for the hormonal signaling pathway leading to meiotic resumption in starfish oocytes

Dev Biol. 2004 Dec 15;276(2):330-6. doi: 10.1016/j.ydbio.2004.08.036.

Abstract

Meiotic resumption is generally under the control of an extracellular maturation-inducing hormone. It is equivalent to the G2-M phase transition in somatic cell mitosis and is regulated by cyclin B-Cdc2 kinase. However, the complete signaling pathway from the hormone to cyclin B-Cdc2 is yet unclear in any organism. A model system to analyze meiotic resumption is the starfish oocyte, in which Akt/protein kinase B (PKB) plays a key mediator in hormonal signaling that leads to cyclin B-Cdc2 activation. Here we show in starfish oocytes that when PDK1 activity is inhibited by a neutralizing antibody, maturation-inducing hormone fails to induce cyclin B-Cdc2 activation at the meiotic G2-M phase transition, even though PDK2 activity becomes detectable. These observations assign a novel role to PDK1 for a hormonal signaling intermediate toward meiotic resumption. They further support that PDK2 is a molecule distinct from PDK1 and Akt, and that PDK2 activity is not sufficient for the full activation of Akt in the absence of PDK1 activity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3-Phosphoinositide-Dependent Protein Kinases
  • Amino Acid Sequence
  • Animals
  • Antibodies / metabolism
  • CDC2 Protein Kinase / metabolism
  • Cyclin B / metabolism
  • Enzyme Activation
  • Growth Substances / metabolism*
  • Meiosis / physiology*
  • Molecular Sequence Data
  • Oocytes / cytology
  • Oocytes / physiology*
  • Phosphorylation
  • Protein Serine-Threonine Kinases / antagonists & inhibitors
  • Protein Serine-Threonine Kinases / genetics
  • Protein Serine-Threonine Kinases / metabolism*
  • Proto-Oncogene Proteins / metabolism
  • Proto-Oncogene Proteins c-akt
  • Sequence Alignment
  • Signal Transduction / physiology*
  • Starfish*

Substances

  • Antibodies
  • Cyclin B
  • Growth Substances
  • Proto-Oncogene Proteins
  • 3-Phosphoinositide-Dependent Protein Kinases
  • Protein Serine-Threonine Kinases
  • Proto-Oncogene Proteins c-akt
  • CDC2 Protein Kinase

Associated data

  • GENBANK/AB110536