Dai Xing-Xing, Wu Yu-Ke, Pi Shuai-Bo, Hu Feng-Jie, Wu Yun-Wen, Qi Hang, Li Zhiyi, Jiang Zhi-Yan, Zhao Long-Wen, Fan Heng-Yu
Department of Obstetrics and Gynecology, Center for Reproductive Medicine, the Fourth Affiliated Hospital of School of Medicine, and International School of Medicine, International Institutes of Medicine, Zhejiang University, Yiwu, 322000, China.
Life Sciences Institute, Zhejiang University, Hangzhou, 310058, China.
Adv Sci (Weinh). 2025 Jun;12(23):e2500048. doi: 10.1002/advs.202500048. Epub 2025 Apr 23.
During oocyte meiosis, maternal transcript polyadenylation is crucial for regulating mRNA stability and translation, which are essential for oocyte maturation. Polyadenylate-binding protein nuclear 1 (PABPN1) plays a key role in regulating mRNA splicing and polyadenylation in somatic cells and growing oocytes. However, its potential function in regulating the meiotic maturation of fully grown oocytes remains unknown. This study reports that selective Pabpn1 knockout in growing mouse oocytes using Zp3-Cre do not affect folliculogenesis but prevented germinal vesicle breakdown in fully grown oocytes, impaired CDK1 activation, and resulted in abnormal spindle formation and chromosome misalignment. The results of poly(A)-inclusive full-length RNA isoform sequencing (PAIso-seq) and transcriptome sequencing revealed that PABPN1 coordinates meiotic maturation-coupled polyadenylation and degradation of maternal mRNAs, which are key factors of maturation-promoting factor (MPF) and deadenylation mediators, such as B-cell translocation gene-4 (BTG4), ensuring proper meiotic progression. The results of rescue experiments indicate these functions of PABPN1 are mediated by its key domains, which interact with poly(A) polymerase and recruit target mRNAs. This study highlighted the physiological importance of cytoplasmic PABPN1 in mammalian oocyte maturation by integrating maternal transcript polyadenylation, translation, and degradation.
在卵母细胞减数分裂过程中,母体转录本的多聚腺苷酸化对于调节mRNA稳定性和翻译至关重要,而这对于卵母细胞成熟必不可少。多聚腺苷酸结合蛋白核1(PABPN1)在体细胞和生长中的卵母细胞中调节mRNA剪接和多聚腺苷酸化方面发挥关键作用。然而,其在调节完全成熟卵母细胞减数分裂成熟中的潜在功能仍不清楚。本研究报告称,使用Zp3-Cre在生长中的小鼠卵母细胞中选择性敲除Pabpn1不会影响卵泡发生,但会阻止完全成熟卵母细胞中的生发泡破裂,损害CDK1激活,并导致纺锤体形成异常和染色体排列紊乱。多聚腺苷酸包含全长RNA异构体测序(PAIso-seq)和转录组测序结果表明,PABPN1协调减数分裂成熟相关的母体mRNA的多聚腺苷酸化和降解,这些母体mRNA是成熟促进因子(MPF)和去腺苷酸化介质(如B细胞易位基因4,BTG4)的关键因素,确保减数分裂的正常进行。拯救实验结果表明,PABPN1的这些功能由其关键结构域介导,这些结构域与多聚腺苷酸聚合酶相互作用并募集靶mRNA。本研究通过整合母体转录本的多聚腺苷酸化、翻译和降解,突出了细胞质PABPN1在哺乳动物卵母细胞成熟中的生理重要性。