eIF3与高度翻译的mRNAs的3'-UTR末端进行交互
Santi Mestre-Fos1,2, Lucas Ferguson2,3, Marena I Trinidad1,4
1Innovative Genomics Institute, University of California, Berkeley, Berkeley, United States.
eLife
|January 29, 2025
概括
细胞启动因子3 (eIF3) 在干细胞分化过程中与高度翻译的mRNA的3'未翻译区域结合. 这表明eIF3在通过mRNA循环化调节蛋白质合成方面发挥了一般作用.
科学领域:
- 分子生物学分子生物学
- 干细胞生物学 干细胞生物学
- 生物化学 生物化学
背景情况:
- 干细胞分化需要增加蛋白质合成.
- 控制这种转化增长的机制,特别是启动因素的作用,尚不清楚.
研究的目的:
- 调查真核发起因子3 (eIF3) 在人类多能干细胞 (hPSC) 衍生的神经原生细胞 (NPC) 分化中的功能.
- 阐明eIF3在早期分化过程中影响翻译的分子机制.
主要方法:
- 使用Quick-irCLIP和替代多基化 (APA) 测序来绘制mRNA上的eIF3结合位点.
- 采用核糖体分析来评估翻译活动和效率.
- 分析了eIF3交叉连接,多化状态和翻译之间的关系.
主要成果:
- eIF3主要与mRNA异型的3'未翻译区域 (3'-UTRs) 交叉链接,该异型位于poly(A) 尾部附近.
- eIF3与3'-UTR末端的结合取决于mRNA多基氨基化.
- 高的eIF3交联与高的mRNA转化活性相关,但不一定是转化效率.
结论:
- eIF3与活跃翻译的mRNAs的3'-UTR末端进行交互,表明潜在的一般调节作用.
- 这些发现支持mRNA循环化机制参与调节干细胞分化过程中的蛋白质合成.
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