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 Trinidad1,4
1Innovative Genomics Institute, University of California, Berkeley, CA, USA.
bioRxiv : the preprint server for biology
|November 21, 2023
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.
- 控制这种转化突发的分子机制尚未完全理解.
- 翻译启动因素,如eIF3在这个过程中的作用在很大程度上是未知的.
研究的目的:
- 研究真核发起因子3 (eIF3) 在人类多能干细胞 (hPSC) 衍生神经前代细胞 (NPC) 早期分化中的作用.
主要方法:
- 使用了快速-irCLIP和替代多化 (APA) 测序.
- 进行了核糖体分析,以评估转化活性.
主要成果:
- 证明了eIF3主要与mRNA异型的3'未翻译区域 (3'-UTR) 末端的交叉链接.
- 发现3'-UTR末端的eIF3参与取决于多基化.
- 观察到3'-UTR终端的高eIF3交联与高转化活性之间的相关性,但不是转化效率.
结论:
- 在NPC分化过程中,eIF3与高度翻译的mRNA的3'-UTR末端进行交互.
- 这表明eIF3在翻译中具有一般的监管功能.
- 支持mRNA循环化在干细胞分化过程中调节mRNA转化中的作用.
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