Department of Biochemistry, Max Planck Institute for Developmental Biology, D-72076 Tübingen, Germany.
Genes Dev. 2020 Jun 1;34(11-12):847-860. doi: 10.1101/gad.336073.119. Epub 2020 Apr 30.
Human 4E-T is an eIF4E-binding protein (4E-BP) present in processing (P)-bodies that represses translation and regulates decay of mRNAs destabilized by AU-rich elements and microRNAs (miRNAs). However, the underlying regulatory mechanisms are still unclear. Here, we show that upon mRNA binding 4E-T represses translation and promotes deadenylation via the recruitment of the CCR4-NOT deadenylase complex. The interaction with CCR4-NOT is mediated by previously uncharacterized sites in the middle region of 4E-T. Importantly, mRNA decapping and decay are inhibited by 4E-T and the deadenylated target is stored in a repressed form. Inhibition of mRNA decapping requires the interaction of 4E-T with the cap-binding proteins eIF4E/4EHP. We further show that regulation of decapping by 4E-T participates in mRNA repression by the miRNA effector protein TNRC6B and that 4E-T overexpression interferes with tristetraprolin (TTP)- and NOT1-mediated mRNA decay. Thus, we postulate that 4E-T modulates 5'-to-3' decay by swapping the fate of a deadenylated mRNA from complete degradation to storage. Our results provide insight into the mechanism of mRNA storage that controls localized translation and mRNA stability in P-bodies.
人 4E-T 是一种 eIF4E 结合蛋白(4E-BP),存在于加工体(P)中,可抑制翻译,并调节由富含 AU 元件和 microRNAs(miRNAs)不稳定的 mRNA 的降解。然而,其潜在的调控机制尚不清楚。在这里,我们发现,4E-T 结合 mRNA 后,通过募集 CCR4-NOT 脱腺苷酸化酶复合物来抑制翻译并促进脱腺苷酸化。与 CCR4-NOT 的相互作用是由 4E-T 中中部区域以前未被表征的位点介导的。重要的是,4E-T 抑制 mRNA 去帽和降解,并且去帽的靶标以受抑制的形式储存。4E-T 与帽结合蛋白 eIF4E/4EHP 的相互作用需要抑制 mRNA 的去帽。我们进一步表明,4E-T 对 decapping 的调控参与了 miRNA 效应蛋白 TNRC6B 对 mRNA 的抑制,并且 4E-T 的过表达会干扰 tristetraprolin (TTP) 和 NOT1 介导的 mRNA 降解。因此,我们假设 4E-T 通过将脱腺苷酸化 mRNA 的命运从完全降解转换为储存,来调节 5'-3' 降解。我们的研究结果为控制 P 体中局部翻译和 mRNA 稳定性的 mRNA 储存机制提供了新的见解。