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多胺通过刺激组蛋白乙酰转移酶 mRNA 的翻译来调节基因表达。

Polyamines regulate gene expression by stimulating translation of histone acetyltransferase mRNAs.

机构信息

Faculty of Pharmacy, Chiba Institute of Science, Choshi, Chiba, Japan.

Amine Pharma Research Institute, Chiba, Japan.

出版信息

J Biol Chem. 2020 Jun 26;295(26):8736-8745. doi: 10.1074/jbc.RA120.013833. Epub 2020 May 6.

Abstract

Polyamines regulate gene expression in by translationally stimulating mRNAs encoding global transcription factors. In this study, we focused on histone acetylation, one of the mechanisms of epigenetic regulation of gene expression, to attempt to clarify the role of polyamines in the regulation of gene expression in eukaryotes. We found that activities of histone acetyltransferases in both the nucleus and cytoplasm decreased significantly in polyamine-reduced mouse mammary carcinoma FM3A cells. Although protein levels of histones H3 and H4 did not change in control and polyamine-reduced cells, acetylation of histones H3 and H4 was greatly decreased in the polyamine-reduced cells. Next, we used control and polyamine-reduced cells to identify histone acetyltransferases whose synthesis is stimulated by polyamines. We found that polyamines stimulate the translation of histone acetyltransferases GCN5 and HAT1. Accordingly, GCN5- and HAT1-catalyzed acetylation of specific lysine residues on histones H3 and H4 was stimulated by polyamines. Consistent with these findings, transcription of genes required for cell proliferation was enhanced by polyamines. These results indicate that polyamines regulate gene expression by enhancing the expression of the histone acetyltransferases GCN5 and HAT1 at the level of translation. Mechanistically, polyamines enhanced the interaction of microRNA-7648-5p (miR-7648-5p) with the 5'-UTR of GCN5 mRNA, resulting in stimulation of translation due to the destabilization of the double-stranded RNA (dsRNA) between the 5'-UTR and the ORF of GCN5 mRNA. Because HAT1 mRNA has a short 5'-UTR, polyamines may enhance initiation complex formation directly on this mRNA.

摘要

多胺通过翻译刺激编码全局转录因子的 mRNA 来调节 中的基因表达。在这项研究中,我们专注于组蛋白乙酰化,这是基因表达表观遗传调控的机制之一,试图阐明多胺在真核生物基因表达调控中的作用。我们发现在多胺减少的鼠乳腺肿瘤 FM3A 细胞中,核和细胞质中的组蛋白乙酰转移酶活性显著降低。尽管组蛋白 H3 和 H4 的蛋白质水平在对照和多胺减少的细胞中没有变化,但组蛋白 H3 和 H4 的乙酰化在多胺减少的细胞中大大减少。接下来,我们使用对照和多胺减少的细胞来鉴定受多胺刺激合成的组蛋白乙酰转移酶。我们发现多胺刺激组蛋白乙酰转移酶 GCN5 和 HAT1 的翻译。因此,多胺刺激组蛋白 H3 和 H4 上特定赖氨酸残基的 GCN5 和 HAT1 催化乙酰化。与这些发现一致,细胞增殖所需基因的转录被多胺增强。这些结果表明,多胺通过增强翻译水平上的组蛋白乙酰转移酶 GCN5 和 HAT1 的表达来调节基因表达。从机制上讲,多胺增强了 microRNA-7648-5p (miR-7648-5p) 与 GCN5 mRNA 5'-UTR 的相互作用,导致双链 RNA (dsRNA) 之间的稳定双螺旋结构由于 GCN5 mRNA 的 5'-UTR 和 ORF 之间的破坏,从而刺激翻译。由于 HAT1 mRNA 具有短的 5'-UTR,多胺可能直接在该 mRNA 上增强起始复合物的形成。

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