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一种新的翻译中解旋酶活性报告分子揭示了 DDX3X 的相互作用。

A novel reporter for helicase activity in translation uncovers DDX3X interactions.

机构信息

Department of Cell and Tissue Biology, University of California, San Francisco, San Francisco, California 94143, USA.

Graduate Division, University of California, San Francisco, San Francisco, California 94143, USA.

出版信息

RNA. 2024 Jul 16;30(8):1041-1057. doi: 10.1261/rna.079837.123.

Abstract

DDX3X regulates the translation of a subset of human transcripts containing complex 5' untranslated regions (5' UTRs). In this study, we developed the helicase activity reporter for translation (HART), which uses DDX3X-sensitive 5' UTRs to measure DDX3X-mediated translational activity in cells. To directly measure RNA structure in DDX3X-dependent mRNAs, we used SHAPE-MaP to determine the secondary structures present in DDX3X-sensitive 5' UTRs and then used HART to investigate how sequence alterations influence DDX3X sensitivity. Additionally, we identified residues 38-44 as potential mediators of DDX3X's interaction with the translational machinery. HART revealed that both DDX3X's association with the translational machinery and its helicase activity are required for its function in promoting the translation of DDX3X-sensitive 5' UTRs. These findings suggest DDX3X plays a crucial role in regulating translation through its interaction with the translational machinery during ribosome scanning and establish the HART reporter as a robust, lentivirally encoded, colorimetric measurement of DDX3X-dependent translation in cells.

摘要

DDX3X 调节含有复杂 5' 非翻译区(5'UTR)的人类转录本的翻译。在这项研究中,我们开发了用于翻译的解旋酶活性报告(HART),它使用 DDX3X 敏感的 5'UTR 来测量细胞中 DDX3X 介导的翻译活性。为了直接测量 DDX3X 依赖性 mRNA 中的 RNA 结构,我们使用 SHAPE-MaP 来确定 DDX3X 敏感的 5'UTR 中存在的二级结构,然后使用 HART 来研究序列改变如何影响 DDX3X 的敏感性。此外,我们确定了残基 38-44 作为 DDX3X 与翻译机制相互作用的潜在介质。HART 表明,DDX3X 与翻译机制的结合及其解旋酶活性对于其促进 DDX3X 敏感的 5'UTR 翻译的功能都是必需的。这些发现表明 DDX3X 通过在核糖体扫描过程中与翻译机制相互作用,在调节翻译中发挥关键作用,并确立 HART 报告作为细胞中 DDX3X 依赖性翻译的稳健、基于慢病毒的比色测量方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0dc/11251518/531ad650f125/1041f01.jpg

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