一个修改通过通过IGF2BP3从多体转换mRNA到P体通过IGF2BP3负面调节翻译
Ting Shan1, Feiyan Liu1, Miaomiao Wen2
1College of Life Sciences, TaiKang Center for Life and Medical Sciences, RNA Institute, Hubei Key Laboratory of Cell Homeostasis, Wuhan University, Wuhan, China; Frontier Science Center for Immunology and Metabolism, State Key Laboratory of Virology, Wuhan University, Wuhan, China.
Molecular cell
|November 28, 2023
概括
N6-甲基氨酸 (m6A) 控制了翻译多体和非翻译P体之间的mRNA局部化. 这种由METTL14和IGF2BP3影响的表观遗传标记,决定了细胞质中的mRNA命运.
科学领域:
- 分子生物学分子生物学
- 表观遗传学 在表观遗传学中,表观遗传学是指表观遗传学.
- 在RNA生物学,RNA生物学.
背景情况:
- 细胞质mRNA存在于翻译 (多体) 和非翻译 (P体) 池中.
- 控制mRNA分区的调控机制在很大程度上是未知的.
研究的目的:
- 阐明N6-甲基氨酸 (m6A) 在调节多体和P体之间的mRNA分区中的作用.
- 为了确定参与m6A介导的mRNA定位的关键蛋白质.
主要方法:
- 在HeLa细胞中使用m-LAIC-seq和m-LC-MS/MS进行A级量化.
- 敲除和分子结合测试以评估蛋白质功能.
- 蛋白质组分析以确定m6A阅读器.
主要成果:
- 多聚体相关的mRNA显示较低的m6A水平,而P体丰富的mRNA显示较高的m6A修饰.
- 降低METTL14的调节通过将mRNA从P体转移到多体体来促进翻译.
- IGF2BP3充当m6读者,调解目标mRNA从多体转向P体的转换.
结论:
- m6A动态调节翻译和非翻译细胞区间之间的mRNA分区.
- 编写器METTL14和阅读器IGF2BP3是这个监管过程中的关键参与者.
- 这项研究提出了一个m6A-依赖mRNA命运决定的模型.
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