eIF4E 可协调 mRNA 处理、RNA 输出和翻译,从而改变特定蛋白质的生成。

Nucleus (Austin, Tex.) Pub Date : 2024-12-01 Epub Date: 2024-06-16 DOI:10.1080/19491034.2024.2360196
Jean-Clément Mars, Biljana Culjkovic-Kraljacic, Katherine L B Borden
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引用次数: 0

摘要

真核翻译起始因子 eIF4E 是一种多功能因子,在许多生物体中同时影响 mRNA 的加工、输出和翻译。eIF4E 的多因素效应源于其与 mRNA 5'end 上的甲基-7-鸟苷酸帽结合的能力,因此可在细胞核和细胞质中充当转录本的帽伴侣。在这篇综述中,我们描述了 eIF4E 在主要 mRNA 处理过程中的多因素作用,包括加帽、剪接、裂解和多腺苷酸化、核输出和翻译。我们讨论的证据表明,eIF4E 在两个层面上发挥作用,对加工、输出和最终生成的蛋白质产生广泛的改变。首先,eIF4E 改变了 mRNA 处理机制成分的产生,支持对多个 mRNA 处理事件进行大规模重编程。这样,eIF4E 就能在不与目标转录本发生物理作用的情况下调节 mRNA 的加工。其次,eIF4E 还能与加帽 mRNA 以及 RNA 处理或翻译机制的组成部分发生物理作用。此外,只有在特定的 mRNA 处理过程中,特定的 mRNA 才会对 eIF4E 敏感。这种选择性受 mRNA 中被称为 USER 代码的顺式作用元件的支配,这些元件可招募相关的辅助因子,使其参与适当的机制。总之,我们描述了 eIF4E 多因素功能的分子基础和相关调控途径,讨论了选择性的基础,列出了在这些活动中发挥作用的约 80 个 eIF4E 相互作用因子,并概述了其功能与其致癌潜力的相关性。最后,我们总结了针对癌症中 eIF4E 的早期临床研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
eIF4E orchestrates mRNA processing, RNA export and translation to modify specific protein production.

The eukaryotic translation initiation factor eIF4E acts as a multifunctional factor that simultaneously influences mRNA processing, export, and translation in many organisms. Its multifactorial effects are derived from its capacity to bind to the methyl-7-guanosine cap on the 5'end of mRNAs and thus can act as a cap chaperone for transcripts in the nucleus and cytoplasm. In this review, we describe the multifactorial roles of eIF4E in major mRNA-processing events including capping, splicing, cleavage and polyadenylation, nuclear export and translation. We discuss the evidence that eIF4E acts at two levels to generate widescale changes to processing, export and ultimately the protein produced. First, eIF4E alters the production of components of the mRNA processing machinery, supporting a widescale reprogramming of multiple mRNA processing events. In this way, eIF4E can modulate mRNA processing without physically interacting with target transcripts. Second, eIF4E also physically interacts with both capped mRNAs and components of the RNA processing or translation machineries. Further, specific mRNAs are sensitive to eIF4E only in particular mRNA processing events. This selectivity is governed by the presence of cis-acting elements within mRNAs known as USER codes that recruit relevant co-factors engaging the appropriate machinery. In all, we describe the molecular bases for eIF4E's multifactorial function and relevant regulatory pathways, discuss the basis for selectivity, present a compendium of ~80 eIF4E-interacting factors which play roles in these activities and provide an overview of the relevance of its functions to its oncogenic potential. Finally, we summarize early-stage clinical studies targeting eIF4E in cancer.

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