Journal
GENE
Volume 887, Issue -, Pages -Publisher
ELSEVIER
DOI: 10.1016/j.gene.2023.147745
Keywords
ASTL; Ovastacin; Female infertility; Polyspermy; in vitro fertilization
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Fertilization of the egg by the sperm is a vital stage of embryogenesis, but polyspermy, which is the entry of multiple sperm into the egg, is generally lethal to the embryo. A recent study identified a gene variant in ASTL that is associated with female infertility characterized by polyspermy. This study further expands the understanding of ASTL mutations and can aid in the diagnosis of oocyte-borne polyspermy.
Fertilization of the egg by the sperm is the first vital stage of embryogenesis. In mammals, only one sperm is incorporated into the oocyte. Polyspermy is a key anomaly of fertilization that is generally lethal to the embryo. To date, only a few causative genes for polyspermy have been reported. In a recent study, a homozygous variant in astacin-like metalloendopeptidase (ASTL), which encodes the ovastacin enzyme that cleaves ZP2 to prevent polyspermy, was found to be associated with female infertility characterized by polyspermy in vitro. Herein, we identified two ASTL variants in a Chinese woman likely responsible for her primary infertility and polyspermy in in vitro fertilization. Both variants were located within the key catalytic domain and predicted to alter hydrogen bonds, potentially impairing protein stability. Moreover, expression and immunoblot analyses in CHO-K1 cells indicated abnormal ovastacin zymogen activation or decreased enzyme stability. Intracytoplasmic sperm injection treatment successfully bypassed the defect in polyspermy blocking and resulted in a live birth. Our study associates ASTL variants with human infertility and further supports the contribution of this gene to blocking polyspermy in humans. Our findings expand the spectrum of ASTL mutations and should facilitate the diagnosis of oocyte-borne polyspermy.
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