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曲古抑菌素 A 通过抑制组蛋白去乙酰化酶 2 和 3 诱导 5-脂氧合酶启动子活性和 mRNA 表达。

Trichostatin A induces 5-lipoxygenase promoter activity and mRNA expression via inhibition of histone deacetylase 2 and 3.

机构信息

Institute of Pharmaceutical Chemistry/ZAFES, Goethe University Frankfurt, Frankfurt, Germany.

出版信息

J Cell Mol Med. 2012 Jul;16(7):1461-73. doi: 10.1111/j.1582-4934.2011.01420.x.

DOI:10.1111/j.1582-4934.2011.01420.x
PMID:21883892
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3823215/
Abstract

The 5-lipoxygenase (5-LO) is the key enzyme in the formation of leukotrienes. We have previously shown that the histone deacetylase (HDAC) inhibitor trichostatin A (TSA) activates 5-LO transcription via recruitment of Sp1, Sp3 and RNA polymerase II to the proximal promoter. To identify the HDACs involved in the regulation of 5-LO promoter activity isoform-specific HDAC inhibitors were applied. 5-LO promoter activity and mRNA expression were up-regulated by the class I HDAC inhibitors apicidin and MS-275 but not by class II inhibitors. Knockdown of HDAC 1, 2 and 3 revealed that HDAC2 and HDAC3 but not HDAC1 is involved in the up-regulation of 5-LO mRNA expression. To analyse the chromatin modifications at the 5-LO promoter associated with HDAC inhibition, the time course of 5-LO mRNA induction by trichostatin A was investigated and the concomitant changes in histone modifications at the 5-LO promoter in HL-60, U937 and Mono Mac6 cells were determined. Chromatin immunoprecipitation analysis revealed that trichostatin A increases acetylation of histones H3 and H4 at the 5-LO core promoter in HL-60 and U937 cells whereas no significant changes were observed in Mono Mac6 cells. The appearance of H3 and H4 acetylation preceded the 5-LO mRNA induction whereas in all three cell lines, induction of 5-LO mRNA expression correlated with histone H3 lysine 4 trimethylation (H3K4me3), a marker for transcriptional activity of gene promoters.

摘要

5-脂氧合酶(5-LO)是白三烯形成的关键酶。我们之前已经表明,组蛋白去乙酰化酶(HDAC)抑制剂曲古抑菌素 A(TSA)通过募集 Sp1、Sp3 和 RNA 聚合酶 II 到近端启动子来激活 5-LO 转录。为了鉴定参与 5-LO 启动子活性调节的 HDAC,应用了同工型特异性 HDAC 抑制剂。I 类 HDAC 抑制剂 apicidin 和 MS-275 上调了 5-LO 启动子活性和 mRNA 表达,但 II 类抑制剂则没有。HDAC1、2 和 3 的敲低表明,HDAC2 和 HDAC3 而非 HDAC1 参与了 5-LO mRNA 表达的上调。为了分析与 HDAC 抑制相关的 5-LO 启动子上的染色质修饰,研究了 TSA 诱导 5-LO mRNA 的时间过程,并确定了 HL-60、U937 和 Mono Mac6 细胞中 5-LO 启动子上组蛋白修饰的伴随变化。染色质免疫沉淀分析表明,TSA 在 HL-60 和 U937 细胞中增加了 5-LO 核心启动子处组蛋白 H3 和 H4 的乙酰化,而在 Mono Mac6 细胞中则没有观察到明显变化。H3 和 H4 乙酰化的出现先于 5-LO mRNA 的诱导,而在所有三种细胞系中,5-LO mRNA 表达的诱导与组蛋白 H3 赖氨酸 4 三甲基化(H3K4me3)相关,H3K4me3 是基因启动子转录活性的标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdff/3823215/a6cf25965d16/jcmm0016-1461-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdff/3823215/8cf82010cd70/jcmm0016-1461-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdff/3823215/5e217e8ccb0b/jcmm0016-1461-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdff/3823215/26682767d1a8/jcmm0016-1461-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdff/3823215/5b8e1f858017/jcmm0016-1461-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdff/3823215/c8fc938b9fa5/jcmm0016-1461-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdff/3823215/e5373bde510c/jcmm0016-1461-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdff/3823215/a6cf25965d16/jcmm0016-1461-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdff/3823215/8cf82010cd70/jcmm0016-1461-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdff/3823215/5e217e8ccb0b/jcmm0016-1461-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdff/3823215/26682767d1a8/jcmm0016-1461-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdff/3823215/5b8e1f858017/jcmm0016-1461-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdff/3823215/c8fc938b9fa5/jcmm0016-1461-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdff/3823215/e5373bde510c/jcmm0016-1461-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdff/3823215/a6cf25965d16/jcmm0016-1461-f7.jpg

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