Maturation promoting factor destabilization facilitates postovulatory aging-mediated abortive spontaneous egg activation in rat

Dev Growth Differ. 2016 Apr;58(3):293-302. doi: 10.1111/dgd.12272. Epub 2016 Mar 17.

Abstract

The present study was designed to investigate whether destabilization of maturation promoting factor (MPF) leads to postovulatory aging-mediated abortive spontaneous egg activation (SEA). If so, we wished to determine whether changes in Wee-1 as well as Emi2 levels are associated with MPF destabilization during postovulatory aging-mediated abortive SEA in rats eggs aged in vivo. For this purpose, sexually immature female rats were given a single injection (20 IU IM) of pregnant mare serum gonadotropin for 48 h followed by single injection of human chorionic gonadotropin (20 IU). Ovulated eggs were collected after 14, 17, 19 and 21 h post-hCG surge to induce postovulatory aging in vivo. The morphological changes, Wee1, phosphorylation status of cyclin dependent kinase 1(Cdk1), early mitotic inhibitor 2 (Emi2), anaphase promoting complex/cyclosome (APC/C), cyclin B1, mitotic arrest deficient protein (MAD2) levels and Cdk1 activity were analyzed. The increased Wee 1 level triggered phosphorylation of Thr-14/Tyr-15 and dephosphorylation of Thr-161 residues of Cdk1. The decrease of Emi2 level was associated with increased APC/C level and decreased cyclin B1 level. Changes in phosphorylation status of Cdk1 and reduced cyclin B1 level resulted in destabilization of MPF. The destabilized MPF finally led to postovulatory aging-mediated abortive SEA in rat eggs. It was concluded that the increase of Wee 1 but decrease of Emi2 level triggers MPF destabilization and thereby postovulatory aging-mediated abortive SEA in rat eggs.

Keywords: Emi2; Wee1; anaphase promoting complex/cyclosome; maturation promoting factor; postovulatory egg aging.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anaphase-Promoting Complex-Cyclosome
  • Animals
  • CDC2 Protein Kinase / metabolism
  • Cellular Senescence / physiology*
  • Chorionic Gonadotropin / pharmacology
  • Cyclin B1 / metabolism
  • F-Box Proteins / metabolism
  • Female
  • Gonadotropins, Equine / pharmacology
  • Horses
  • Humans
  • Mad2 Proteins / metabolism
  • Maturation-Promoting Factor / metabolism*
  • Microscopy, Fluorescence
  • Oocytes / cytology
  • Oocytes / metabolism
  • Oocytes / physiology*
  • Ovulation / drug effects
  • Ovulation / physiology*
  • Phosphorylation
  • Protein-Tyrosine Kinases / metabolism
  • Rats
  • Threonine / metabolism
  • Time Factors

Substances

  • Chorionic Gonadotropin
  • Cyclin B1
  • Emi2 protein, rat
  • F-Box Proteins
  • Gonadotropins, Equine
  • Mad2 Proteins
  • Threonine
  • Anaphase-Promoting Complex-Cyclosome
  • Wee1 protein, rat
  • Protein-Tyrosine Kinases
  • CDC2 Protein Kinase
  • Maturation-Promoting Factor