Molecular determinants of the meiotic arrests in mammalian oocytes at different stages of maturation

Saffet Ozturk1

  • 1Department of Histology and Embryology, Akdeniz University School of Medicine, Antalya, Turkey.

Insights

Mammalian oocytes normally arrest during maturation but can experience permanent arrest due to gene expression changes or assisted reproductive technologies. This review explores molecular causes and potential solutions for oocyte maturation arrests.

Area of Science:

  • Reproductive Biology
  • Developmental Biology
  • Cell Biology

Background:

  • Mammalian oocytes exhibit two crucial developmental arrests during meiosis: prophase I and metaphase II.
  • These arrests are regulated by follicular cells producing cAMP and cGMP to control maturation promoting factor (MPF) levels.
  • Permanent oocyte arrests can occur at germinal vesicle (GV), metaphase I (MI), or metaphase II (MII) stages.

Purpose of the Study:

  • To comprehensively review the molecular determinants of normal developmental and abnormal permanent arrests in mammalian oocytes.
  • To evaluate the impact of assisted reproductive technologies (ART) on oocyte maturation and permanent arrest formation.
  • To discuss potential strategies for inducing permanent arrests to yield competent oocytes.

Main Methods:

  • Literature review of molecular mechanisms regulating oocyte maturation and arrest.
  • Analysis of oocyte-related gene expression and its role in nuclear and cytoplasmic maturation.
  • Evaluation of chemical agents and conditions used in ART and their contribution to permanent arrests.

Main Results:

  • Permanent oocyte arrests may result from the absence or altered expression of critical oocyte-related genes.
  • ART procedures, including ovarian stimulation and in vitro culture, can contribute to permanent oocyte arrests.
  • The number of permanently arrested oocytes in ART centers is increasing.

Conclusions:

  • Understanding the molecular basis of oocyte arrest is crucial for improving ART outcomes.
  • Further research into gene regulation and ART conditions is needed to mitigate permanent oocyte arrests.
  • Developing methods to induce controlled permanent arrests could enhance oocyte competence for fertility treatments.

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