转录基因剖析揭示了老鼠卵细胞的双相调节不稳定性和晚期蛋白静态衰退
Phuong Thanh N Dinh1, Seung Hwan Lee2, Inchul Choi2
1Department of Bio-AI Convergence, Chungnam National University, Daejeon 34134, Republic of Korea.
Genes
|January 28, 2026
概括
母亲的衰老通过两阶段的过程导致卵细胞功能障碍. 中年会引发显著的分子变化,导致生殖衰老和不孕.
科学领域:
- 生殖生物学 生殖生物学
- 分子生物学分子生物学
- 衰老研究研究 衰老研究
背景情况:
- 母亲老龄化对卵细胞质量和生育能力产生负面影响.
- 在整个生殖寿命中,卵细胞衰老的基础分子机制尚未完全理解.
研究的目的:
- 定义不同生殖阶段的小鼠卵细胞的转录形态.
- 为了阐明卵细胞衰老的分子轨迹.
主要方法:
- 从年轻,中年和老年小鼠的小鼠生殖囊泡 (GV) 卵细胞的转录形状分析.
- 生物信息分析,包括差异基因表达 (DEG) 分析和转录因子结合位点 (TFBS) 分析.
主要成果:
- 卵细胞衰老遵循一个双相,非线性轨迹.
- 从年轻人到中年人的过渡显示出显著的转录不稳定 (1197 DEGs) 影响代谢和信号网络,可能是由表观遗传修饰而不是转录因子枯竭驱动的.
- 从中年到老年过渡的特点是线粒体功能障碍和蛋白质静态压力,表明系统性崩.
结论:
- 卵细胞衰老是一种双相过程,涉及补偿性抵抗,其次是系统性崩.
- 中年代表了对卵细胞调控重塑的关键转折点.
- 这些发现为制定打击与年龄有关的不孕症策略提供了分子基础.
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