The mammalian female reproductive axis is the first to fail in aging; however, the molecular mechanisms underpinning this failure are largely unknown, particularly in oocytes (Chamani & Keefe, 2019;Garg & Sinclair, 2015;Homer, 2020). Fertility in women begins to decline significantly by their mid-30 s and pregnancies in women of advanced age lead to higher rates of miscarriage and/or aneuploid offspring (Baired et al., 2005). Despite these risks, women and couples often postpone pregnancy to a more convenient time which has led to a decline in birthrate among most industrialized societies (Homer, 2020;Navot et al., 1991). This decline in fertility can be explained by the age-related decline in oocyte quality which manifests itself by chromosomal abnormalities, spindle defects, mi-