Oocyte-specific Wee1-like protein kinase 2 is dispensable for fertility in mice

• Published in: PloS one 2023-08, Vol.18 (8), p.e0289083
• Main Authors: Nozawa, Kaori, Liao, Zian, Satouh, Yuhkoh, Geng, Ting, Ikawa, Masahito, Monsivais, Diana, Matzuk, Martin M
• Format: Article
• Language: English
• Subjects: Analysis; Animal models; Animals; Biology and Life Sciences; Cell cycle; Cell Cycle Proteins - genetics; Cell Cycle Proteins - metabolism; Contraception; Contraceptives; CRISPR; Cyclin-dependent kinases; Deletion; Embryos; Engineering and Technology; Exons; Fecundity; Female; Females; Fertility; Fertility - genetics; Frameshift mutation; Gametocytes; Health aspects; Histology; Humans; In vitro fertilization; Infertility; Kinases; Litter size; Medicine; Medicine and Health Sciences; Meiosis; Mice; Mutation; Oocytes; Oocytes - metabolism; Ovaries; Ovulation; Phenotypes; Phosphorylation; Prophase; Protein interaction; Protein Kinases - metabolism; Protein-protein interactions; Protein-tyrosine kinase; Protein-Tyrosine Kinases - genetics; Protein-Tyrosine Kinases - metabolism; Proteins; Research and Analysis Methods; Statistical significance; Surgery; Tyrosine
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0289083

Wee1-like protein kinase 2 (WEE2) is an oocyte-specific protein tyrosine kinase involved in the regulation of oocyte meiotic arrest in humans. As such, it has been proposed as a candidate for non-hormonal female contraception although pre-clinical models have not been reported. Therefore, we developed two novel knockout mouse models using CRISPR/Cas9 to test loss-of-function of Wee2 on female fertility. A frameshift mutation at the Wee2 translation start codon in exon 2 had no effect on litter size, litter production, or the ability of oocytes to maintain prophase I arrest. Because of the lack of a reproductive phenotype, we additionally generated a Wee2 allele with a large deletion by removing all coding exons. While there was no difference in the total number of litters produced, homozygous Wee2 female knockout mice with the larger deletion produced fewer pups than heterozygous littermates. Furthermore, there was no difference for key reproductive parameters measured in the mouse models, including ovarian weight, number of ovulated oocytes, or oocytes that underwent in vitro maturation. Therefore, as loss of Wee2 in mice shows only minor effects on overall fecundity, contraceptive development with WEE2 should consider exploiting alternative properties such as gain-of-function or protein-protein interactions, as Wee2 loss-of-function is likely complicated by biological redundancies with other proteins co-expressed in oocytes.