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多胺通过调节 JunD mRNA 3'非翻译区与 HuR 和 AUF1 的竞争结合来调节其稳定性。

Polyamines regulate the stability of JunD mRNA by modulating the competitive binding of its 3' untranslated region to HuR and AUF1.

机构信息

Department of Surgery, University of Maryland School of Medicine, Baltimore, Maryland 21201, USA.

出版信息

Mol Cell Biol. 2010 Nov;30(21):5021-32. doi: 10.1128/MCB.00807-10. Epub 2010 Aug 30.

Abstract

Polyamines critically regulate all mammalian cell growth and proliferation by mechanisms such as the repression of growth-inhibitory proteins, including JunD. Decreasing the levels of cellular polyamines stabilizes JunD mRNA without affecting its transcription, but the exact mechanism whereby polyamines regulate JunD mRNA degradation has not been elucidated. RNA-binding proteins HuR and AUF1 associate with labile mRNAs bearing AU-rich elements located in the 3' untranslated regions (3'-UTRs) and modulate their stability. Here, we show that JunD mRNA is a target of HuR and AUF1 and that polyamines modulate JunD mRNA degradation by altering the competitive binding of HuR and AUF1 to the JunD 3'-UTR. The depletion of cellular polyamines enhanced HuR binding to JunD mRNA and decreased the levels of JunD transcript associated with AUF1, thus stabilizing JunD mRNA. The silencing of HuR increased AUF1 binding to the JunD mRNA, decreased the abundance of HuR-JunD mRNA complexes, rendered the JunD mRNA unstable, and prevented increases in JunD mRNA and protein in polyamine-deficient cells. Conversely, increasing the cellular polyamines repressed JunD mRNA interaction with HuR and enhanced its association with AUF1, resulting in an inhibition of JunD expression. These results indicate that polyamines modulate the stability of JunD mRNA in intestinal epithelial cells through HuR and AUF1 and provide new insight into the molecular functions of cellular polyamines.

摘要

多胺通过抑制生长抑制蛋白(包括 JunD)等机制来严格调节所有哺乳动物细胞的生长和增殖。降低细胞内多胺的水平可以稳定 JunD mRNA,而不影响其转录,但多胺调节 JunD mRNA 降解的确切机制尚未阐明。RNA 结合蛋白 HuR 和 AUF1 与含有富含 AU 元件的不稳定 mRNA 结合,这些元件位于 3'非翻译区(3'-UTR),并调节其稳定性。在这里,我们表明 JunD mRNA 是 HuR 和 AUF1 的靶标,多胺通过改变 HuR 和 AUF1 对 JunD 3'-UTR 的竞争结合来调节 JunD mRNA 降解。细胞多胺的耗竭增强了 HuR 与 JunD mRNA 的结合,降低了与 AUF1 相关的 JunD 转录本水平,从而稳定了 JunD mRNA。HuR 的沉默增加了 AUF1 与 JunD mRNA 的结合,减少了 HuR-JunD mRNA 复合物的丰度,使 JunD mRNA 不稳定,并防止在多胺缺乏的细胞中 JunD mRNA 和蛋白的增加。相反,增加细胞内多胺会抑制 JunD mRNA 与 HuR 的相互作用,并增强其与 AUF1 的结合,从而抑制 JunD 的表达。这些结果表明,多胺通过 HuR 和 AUF1 调节肠上皮细胞中 JunD mRNA 的稳定性,并为细胞多胺的分子功能提供了新的见解。

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