IF 5.3 2区 医学 Q2 CELL BIOLOGY Cell Biology and Toxicology Pub Date : 2025-02-20 DOI:10.1007/s10565-025-09999-1
Xia Jiang, Weiwei Xu, Jiandong Sun, Jianmin Lin, Zihang Lin, Xiuli Lian, Shumin Liao, Shanshan Luo, Yue Liu, Shie Wang
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引用次数: 0

摘要

尽管子代基因组激活(ZGA)对早期胚胎发育至关重要,但其在哺乳动物中的调控机制仍不清楚。在本研究中,我们证明了母源因子 TRPS1 在小鼠早期胚胎发育中发挥着重要作用,它在胚胎植入前发育过程中调控 2 细胞胚胎向 4 细胞胚胎的过渡。Trps1的缺失可通过AKT/CREB信号通路导致ZGA受损。此外,我们的研究结果表明,TRPS1可能会调节Pde4d的转录,从而影响AKT和CREB的磷酸化。有趣的是,与单独敲除 Trps1 相比,联合注射 Trps1 siRNA 和 Pde4d mRNA 能显著提高 4 细胞胚胎的发育速度。总之,这些结果表明,Trps1通过靶向PDE4D/AKT/CREB途径调控ZGA,在小鼠植入前胚胎发育过程中起到了负面作用。
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Trps1 regulates mouse zygotic genome activation and preimplantation embryo development via the PDE4D/AKT/CREB signaling pathway.

Despite zygotic genome activation (ZGA) is crucial for early embryonic development, its regulatory mechanism is still unclear in mammals. In the present study, we demonstrate that TRPS1, a maternal factor, plays an essential role in mouse early embryogenesis by regulating the transition from 2-cell to 4-cell embryos during preimplantation development. The absence of Trps1 could leads to impaired ZGA through AKT/CREB signaling pathway. Furthermore, our findings suggest that TRPS1 may modulate the transcription of Pde4d to influence AKT and CREB phosphorylation. Interestingly, compared to Trps1 knockdown alone, co-injection of Trps1 siRNA and Pde4d mRNA significantly enhances the development rate of 4-cell embryos. Collectively, these results indicate a negative involvement of Trps1 in mouse preimplantation embryo development by targeting the PDE4D/AKT/CREB pathway to regulate ZGA.

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来源期刊
Cell Biology and Toxicology
Cell Biology and Toxicology 生物-毒理学
CiteScore
9.90
自引率
4.90%
发文量
101
审稿时长
>12 weeks
期刊介绍: Cell Biology and Toxicology (CBT) is an international journal focused on clinical and translational research with an emphasis on molecular and cell biology, genetic and epigenetic heterogeneity, drug discovery and development, and molecular pharmacology and toxicology. CBT has a disease-specific scope prioritizing publications on gene and protein-based regulation, intracellular signaling pathway dysfunction, cell type-specific function, and systems in biomedicine in drug discovery and development. CBT publishes original articles with outstanding, innovative and significant findings, important reviews on recent research advances and issues of high current interest, opinion articles of leading edge science, and rapid communication or reports, on molecular mechanisms and therapies in diseases.
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