WDR62 regulates mouse oocyte meiotic maturation related to p-JNK and H3K9 trimethylation. (March 2022)

• Record Type: Journal Article
• Authors: Wang, Yong-Sheng; Chen, Chao; Ahmad, Muhammad Jamil; Chen, Fan; Ding, Zhi-Ming; Yang, Sheng-Ji; Chen, Yang-Wu; Duan, Ze-Qun; Liu, Ming; Liang, Ai-Xin; He, Chang-Jiu; Hua, Guo-Hua; Huo, Li-Jun
• Is Part Of: International journal of biochemistry & cell biology. Volume 144(2022)
• Publication Date: 2022-03
• Subjects: WDR62 -- Oocyte -- Spindle assembly -- Meiotic progression -- P-JNK -- H3K9me3; Biochemistry -- Periodicals; Cytology -- Periodicals; Biochemistry -- Periodicals; Cell Biology -- Periodicals; Biochimie -- Périodiques; Cytologie -- Périodiques; Biochimie; Cytologie; Biochemistry; Cytology; Ressource Internet (Descripteur de forme); Périodique électronique (Descripteur de forme); Periodicals; 572.05
• DOI: 10.1016/j.biocel.2022.106169
• Languages: English
• ISSNs: 1357-2725

Abstract

Abstract: WDR62 (WD40-repeat protein 62) participates in diverse biological process, especially mitotic spindle organization via regulating centriole biogenesis and the function of centriole-associated protein. However, the role of WDR62 exerts in spindle assembly and meiotic progression control in oocytes lacking typical centrosomes remains obscure. In a previous study, we reported that WDR62 is involved in spindle migration and asymmetric cytokinesis in mouse oocyte meiosis. In the current study, another novel function of WDR62 regulating cell cycle progression through meiotic spindle formation during oocyte meiotic maturation was found. Knockdown of WDR62 through siRNA microinjection disrupted the meiotic cell cycle and induced metaphase-I (MI) arrest coupled with severe spindle abnormality, chromosome misalignment, and aneuploid generation. Moreover, WDR62 depletion induced defective kinetochore-microtubule attachments (K-MT) and activated spindle assembly checkpoint (SAC), which could trigger the arrest of meiotic progression. Further study demonstrated that depletion of WDR62 was associated with an aberrant location of p-JNK and reduced its expression level; concomitantly, status of H3K9 trimethylation was also altered. In addition, phenotypes similar to WDR62 depletion were observed during the function-loss analysis of p-JNK using a specific inhibitor (SP600125), which signifies that WDR62 is important for spindle organization and meiotic progression, and this function might be via its regulation of p-JNK. In conclusion, this study revealed that WDR62 functions in multiple ways during oocyte meiotic maturation, which could be related to p-JNK and H3K9 trimethylation. Graphical Abstract: ga1 Highlights: WDR62 knockdown disrupted oocyte meiotic spindle assembly and K-MT attachments. WDR62 depletion caused SAC continuous activation and impaired meiotic progression. WDR62 depletion compromised the activities of p-JNK in mouse oocytes. WDR62 depletion altered H3K9 trimethylation in mouse oocytes.