The role of transcription in EGF- and FSH-mediated oocyte maturation in vitro

Anim Reprod Sci. 2007 Mar;98(1-2):97-112. doi: 10.1016/j.anireprosci.2006.10.007. Epub 2006 Oct 13.

Abstract

Understanding mechanisms responsible for meiotic resumption in mammalian oocytes is critical for the identification of strategies to enhance developmental competence of in vitro-matured oocytes. Improvement of in vitro oocyte maturation systems is dependent on a better understanding of mechanisms that regulate oocyte maturation both in vivo and in vitro as well as on the identification of methods to manipulate the meiotic progression of oocytes matured in vitro in a physiological manner. The purpose of this review is two-fold: first, to examine the mechanisms that underlie the acquisition of oocyte developmental competence and regulation of oocyte maturation in vivo and in vitro; second, to present data examining the role of transcription in mediating the ability of EGF and FSH to induce oocyte maturation in vitro. Results presented support the conclusions that (1) EGF-induced oocyte maturation does not require nascent gene transcription in both mice and domestic cats; (2) FSH requires gene transcription to induce oocyte maturation in both species; (3) EGF must be present in the maturation medium to optimize the effectiveness of FSH to promote oocyte maturation; (4) the mechanism used by FSH to induce oocyte maturation in vitro appears to predominate over that used by EGF when both EGF and FSH are present in maturation medium used for either murine or feline cumulus oocyte complexes.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Cell Culture Techniques
  • Dichlororibofuranosylbenzimidazole / pharmacology
  • Epidermal Growth Factor / pharmacology*
  • Female
  • Follicle Stimulating Hormone / pharmacology*
  • Horses
  • Mammals
  • Mice
  • Mitosis
  • Oocytes / drug effects
  • Oocytes / physiology*
  • Transcription, Genetic*

Substances

  • Dichlororibofuranosylbenzimidazole
  • Epidermal Growth Factor
  • Follicle Stimulating Hormone