Oocyte Developmental Competence and Its Role in Fertility and Reproductive Aging
Oluwaseyi Emmanuel Kolawole
Department of Anatomy, Babcock University, Ilishan Remo, Ogun State, Nigeria.
Faith Tobore Edafetanure
Department of Data Sciences, Harrisburg University of Science and Technology, Pennsylvania, USA.
Onyema Kelechi Roselyn
Department of Anatomy, Babcock University, Ilishan Remo, Ogun State, Nigeria.
Ifeanyi Raphael Ugwuanyi
Department of Physical Sciences, Eastern New Mexico University, New Mexico, USA.
Oluwatobi Quadri
Department of Microbiology and Molecular Genetics, Oklahoma State University, Oklahoma, USA.
Jesse Samson Dogo
British Community Hospital and Outpatient Clinics, Abuja, Nigeria.
Augusta Imomon
University of Nigeria, Université Côte d’Azur, Nsukka, Nigeria.
Okeoghene Marcel Edafetanure-Ibeh
School of Public Health, Texas A&M University, Texas, United States.
Michael Kyere
Department of Biology, Texas A & M University, College Station, Texas, USA.
Possible Okikiola Popoola *
Department of Genome and Molecular Science, Helix Biogen Institute, Ogbomoso, Nigeria.
*Author to whom correspondence should be addressed.
Abstract
Oocyte developmental competence is a fundamental determinant of reproductive success, defined as the ability of an oocyte to complete meiotic maturation, undergo successful fertilization, and support embryonic development through implantation and fetal growth. The acquisition of this competence is a highly coordinated process that occurs during oogenesis and folliculogenesis and involves complex interactions between the oocyte and its surrounding somatic cells within the follicular microenvironment. These interactions regulate a network of molecular and cellular pathways, including nuclear and cytoplasmic maturation, mitochondrial metabolism, epigenetic programming, and the accumulation of maternal RNAs and proteins that sustain early embryogenesis prior to embryonic genome activation. Disruptions in these processes can compromise oocyte quality and significantly reduce fertility outcomes. A major factor influencing oocyte competence is reproductive ageing, which is associated with progressive mitochondrial dysfunction, increased oxidative stress, accumulation of DNA damage, and deterioration of chromosomal cohesion. These age-related alterations contribute to meiotic spindle instability and elevated rates of chromosomal segregation errors, leading to an increased incidence of aneuploidy, implantation failure, and miscarriage. In addition, changes in the follicular microenvironment, including altered endocrine signalling and impaired communication between the oocyte and surrounding granulosa and cumulus cells, further exacerbate the decline in oocyte quality with advancing maternal age. In assisted reproductive technologies (ART), the intrinsic quality of the oocyte remains a critical limiting factor despite advances in embryo culture and genetic screening. Consequently, significant research efforts are directed toward identifying reliable biomarkers that reflect the molecular determinants of oocyte competence. Emerging approaches include transcriptomic analysis of cumulus cells, metabolomic profiling of follicular fluid, and assessment of mitochondrial function and oxidative stress status. These strategies aim to improve the prediction of fertilization potential, embryo developmental capacity, and implantation success. This review synergises current knowledge regarding biological and molecular mechanisms regulating oocyte developmental competence and examines how these processes influence fertility outcomes and reproductive aging. Emphasis is placed on the roles of mitochondrial function, chromosomal stability, metabolic regulation, and follicular signalling in determining oocyte quality. Furthermore, the review discusses emerging biomarkers and clinical strategies aimed at improving oocyte assessment and optimising assisted reproductive treatments. Advancing our understanding of the mechanisms underlying oocyte competence will be essential for improving fertility management, enhancing the success of assisted reproduction, and addressing the challenges associated with reproductive ageing.
Keywords: Oocyte development, fertility, reproductive age, fetal growth, folliculogenesis