Hu Fen, Wang Kai, Zhang Yunfeng, Gou Lixia, Luo Mengmeng, Zhang Xiujun, Yang Shuang
College of Life Sciences, Hebei United University, Tangshan, Hebei 063000, P.R. China.
Department of Life Sciences, Tangshan Normal University, Tangshan, Hebei 063000, P.R. China.
Exp Ther Med. 2014 Jan;7(1):161-164. doi: 10.3892/etm.2013.1376. Epub 2013 Oct 31.
The zinc finger-homeodomain transcription factor, δ-crystallin enhancer factor 1 (δEF1) has been identified as a regulatory factor involved in the promotion of breast cancer cell proliferation via the downregulation of p21 and the upregulation of cyclin-dependent kinase-2 (CDK2) and CDK4 expression. However, the molecular mechanisms underlying the regulation of CDK4 expression by δEF1 have not yet been elucidated. The present study demonstrated that the ectopic expression of δEF1 in MDA-MB-231 breast cancer cells significantly increased the activity of the CDK4 promoter. Deletion of the E2-box (CACGTG), which is located at position -197/-191 on the human CDK4 promoter, significantly attenuated the activation of CDK4 transcription by δEF1. In addition, a CDK4 promoter-M construct was generated via site-directed mutagenesis of the E2-box on the human CDK4 promoter. Luciferase assay showed that the activation of CDK4 promoter-M activity by δEF1 was markedly decreased compared with the CDK4-promoter-0.4k promoter. Knockdown of δEF1 using RNA interference resulted in the inhibition of CDK4 promoter activity. These observations suggest that δEF1 upregulates CDK4 transcription via the E2-box element on the CDK4 promoter.
锌指-同源结构域转录因子δ-晶体蛋白增强因子1(δEF1)已被确定为一种调节因子,它通过下调p21以及上调细胞周期蛋白依赖性激酶2(CDK2)和CDK4的表达来促进乳腺癌细胞增殖。然而,δEF1调控CDK4表达的分子机制尚未阐明。本研究表明,在MDA-MB-231乳腺癌细胞中异位表达δEF1可显著增加CDK4启动子的活性。位于人CDK4启动子-197/-191位置的E2盒(CACGTG)缺失,可显著减弱δEF1对CDK4转录的激活作用。此外,通过对人CDK4启动子上的E2盒进行定点诱变,构建了CDK4启动子-M。荧光素酶检测显示,与CDK4启动子-0.4k启动子相比,δEF1对CDK4启动子-M活性的激活作用明显降低。利用RNA干扰敲低δEF1可导致CDK4启动子活性受到抑制。这些观察结果表明,δEF1通过CDK4启动子上的E2盒元件上调CDK4转录。