聚腺苷酸
生发泡
卵母细胞
细胞生物学
生物
RNA剪接
减数分裂
转录组
体细胞
信使核糖核酸
遗传学
基因
基因表达
核糖核酸
胚胎
作者
Xing‐Xing Dai,Yuke Wu,Shuai‐Bo Pi,Fuliang Hu,Yun‐Wen Wu,Hang Qi,Zhiyan Jiang,Long‐Wen Zhao,Heng‐Yu Fan
标识
DOI:10.1002/advs.202500048
摘要
Abstract 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.
科研通智能强力驱动
Strongly Powered by AbleSci AI