Department of Human Genetics, Aarhus University, Denmark.
Mol Carcinog. 2011 Aug;50(8):601-13. doi: 10.1002/mc.20755. Epub 2011 Mar 3.
The three mammalian HP1 proteins, HP1α/CBX5, HP1β/CBX1, and HPγ/CBX3, are involved in chromatin packing and gene regulation. The HP1α protein is down-regulated in invasive compared to non-invasive breast cancer cells and HP1α is a suppressor of cell migration and invasion. In this report, we examined the background for HP1α protein down-regulation in invasive breast cancer cells. We identified a strict correlation between HP1α down-regulation at the protein level and the mRNA level. The HP1α mRNA down-regulation in invasive cancer cells was not caused by mRNA destabilization. Chromatin immunoprecipitation analysis of the HP1α gene showed a decrease in the histone mark for transcriptional activity H3-K36 tri-methylation and RNA polymerase II in invasive breast cancer cells which correlated with a decreased abundance of basal transcription factors at the HP1α promoter. E2F transcription factors regulate HP1α transcription and we identified that E2F5 depletion increased HP1α expression in invasive breast cancer cells. Finally, we have characterized two HP1α mRNA isoforms and both HP1α mRNA isoforms were down-regulated to a similar extend at the transcriptional level in invasive breast cancer cells. Collectively the presented results show that HP1α down-regulation in invasive breast cancer cells is primary a transcriptional effect and demonstrates a novel set of mechanisms involved in HP1α transcriptional regulation. The finding that HP1α is down-regulated primarily at the transcriptional level provides a new insight for the further elucidation of the detailed molecular mechanisms causing the HP1α down-regulation in invasive breast cancer cells.
三种哺乳动物的 HP1 蛋白(HP1α/CBX5、HP1β/CBX1 和 HPγ/CBX3)参与染色质包装和基因调控。与非浸润性乳腺癌细胞相比,浸润性乳腺癌细胞中 HP1α 蛋白表达下调,HP1α 是细胞迁移和侵袭的抑制剂。在本报告中,我们研究了浸润性乳腺癌细胞中 HP1α 蛋白下调的背景。我们发现 HP1α 蛋白水平和 mRNA 水平的下调之间存在严格的相关性。浸润性癌细胞中 HP1α mRNA 的下调不是由于 mRNA 不稳定引起的。HP1α 基因的染色质免疫沉淀分析显示,转录活性的组蛋白标记 H3-K36 三甲基化和 RNA 聚合酶 II 在浸润性乳腺癌细胞中减少,这与 HP1α 启动子处基本转录因子的丰度降低相关。E2F 转录因子调节 HP1α 的转录,我们发现 E2F5 耗竭增加了浸润性乳腺癌细胞中 HP1α 的表达。最后,我们对两种 HP1α mRNA 异构体进行了特征描述,在浸润性乳腺癌细胞中,两种 HP1α mRNA 异构体在转录水平上的下调程度相似。综上所述,这些结果表明,浸润性乳腺癌细胞中 HP1α 的下调主要是转录效应,并证明了参与 HP1α 转录调控的一组新机制。HP1α 主要在转录水平下调的发现为进一步阐明导致浸润性乳腺癌细胞中 HP1α 下调的详细分子机制提供了新的见解。