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eIF5A 促进翻译延伸、多核糖体解体和应激颗粒组装。

eIF5A promotes translation elongation, polysome disassembly and stress granule assembly.

机构信息

Division of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital, Boston, Massachusetts, United States of America.

出版信息

PLoS One. 2010 Apr 1;5(4):e9942. doi: 10.1371/journal.pone.0009942.

Abstract

Stress granules (SGs) are cytoplasmic foci at which untranslated mRNAs accumulate in cells exposed to environmental stress. We have identified ornithine decarboxylase (ODC), an enzyme required for polyamine synthesis, and eIF5A, a polyamine (hypusine)-modified translation factor, as proteins required for arsenite-induced SG assembly. Knockdown of deoxyhypusine synthase (DHS) or treatment with a deoxyhypusine synthase inhibitor (GC7) prevents hypusine modification of eIF5A as well as arsenite-induced polysome disassembly and stress granule assembly. Time-course analysis reveals that this is due to a slowing of stress-induced ribosome run-off in cells lacking hypusine-eIF5A. Whereas eIF5A only marginally affects protein synthesis under normal conditions, it is required for the rapid onset of stress-induced translational repression. Our results reveal that hypusine-eIF5A-facilitated translation elongation promotes arsenite-induced polysome disassembly and stress granule assembly in cells subjected to adverse environmental conditions.

摘要

应激颗粒(SGs)是细胞暴露于环境应激时未翻译的 mRNA 聚集在细胞质中的焦点。我们已经鉴定出鸟氨酸脱羧酶(ODC)和 eIF5A,一种多胺(hypusine)修饰的翻译因子,作为砷酸盐诱导的 SG 组装所必需的蛋白质。脱氧鸟氨酸合酶(DHS)的敲低或用脱氧鸟氨酸合酶抑制剂(GC7)处理可防止 eIF5A 的 hypusine 修饰以及砷酸盐诱导的多核糖体解聚和应激颗粒组装。时程分析表明,这是由于缺乏 hypusine-eIF5A 的细胞中应激诱导的核糖体流出速度减慢所致。虽然 eIF5A 在正常条件下对蛋白质合成的影响很小,但它是应激诱导的翻译抑制的快速起始所必需的。我们的结果表明,hypusine-eIF5A 促进的翻译延伸促进了在不利环境条件下的细胞中砷酸盐诱导的多核糖体解聚和应激颗粒组装。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7a0/2848580/e30ed3979688/pone.0009942.g001.jpg

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