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组蛋白去乙酰化酶抑制剂阿皮西丁通过Sp1位点激活p21(WAF1/Cip1)转录:蛋白激酶C的参与

Activation of p21(WAF1/Cip1) transcription through Sp1 sites by histone deacetylase inhibitor apicidin: involvement of protein kinase C.

作者信息

Han J W, Ahn S H, Kim Y K, Bae G U, Yoon J W, Hong S, Lee H Y, Lee Y W, Lee H W

机构信息

Department of Biochemistry and Molecular Biology, College of Pharmacy and the Department of Genetic Engineering, College of Life Science and Natural Resources, Sungkyunkwan University, Suwon 440-746, Korea.

出版信息

J Biol Chem. 2001 Nov 9;276(45):42084-90. doi: 10.1074/jbc.M106688200. Epub 2001 Sep 10.

Abstract

We previously reported that apicidin, a novel histone deacetylase inhibitor, inhibited the proliferation of tumor cells via induction of p21(WAF1/Cip1). In this study, we determined the molecular mechanisms by which apicidin induced the p21(WAF1/Cip1) gene expression in HeLa cells. Apicidin induced p21(WAF1/Cip1) mRNA independent of the de novo protein synthesis and activated the p21(WAF1/Cip1) promoter through Sp1-3 site located at -82 and -77 relative to the transcription start site. This transcriptional activation appears to be mediated by protein kinase C (PKC), because calphostin C, a PKC inhibitor, significantly attenuated the activation of p21(WAF1/Cip1) promoter via Sp1 sites, which was accompanied by a marked suppression of p21(WAF1/Cip1) mRNA and protein expression induced by apicidin. Consistent with the transcriptional activation of p21(WAF1/Cip1) promoter by apicidin, apicidin treatment led to the translocation of PKCepsilon from cytosolic to particulate fraction, which was reversed by pretreatment with calphostin C, indicating the involvement of PKC in the transcriptional activation of p21(WAF1/Cip1) via Sp1 sites by apicidin. However, the PKC-mediated transcriptional activation of p21(WAF1/Cip1) by apicidin appears to be independent of the histone hyperacetylation, because apicidin-induced histone hyperacetylation was not affected by calphostin C. Furthermore, a PKC activator, phorbol 12,13-dibutyrate, alone induced the transcriptional activation of p21(WAF1/Cip1) promoter, p21(WAF1/Cip1) mRNA, and protein expression without induction of the histone hyperacetylation, suggesting that the transcriptional activation of p21(WAF1/Cip1) by apicidin might have been mediated by a mechanism other than chromatin remodeling through the histone hyperacetylation. Taken together, these results suggest that the PKC signaling pathway plays a pivotal role in the transcriptional activation of the p21(WAF1/Cip1) gene by apicidin.

摘要

我们之前报道过,新型组蛋白脱乙酰酶抑制剂阿皮西丁通过诱导p21(WAF1/Cip1)抑制肿瘤细胞增殖。在本研究中,我们确定了阿皮西丁在HeLa细胞中诱导p21(WAF1/Cip1)基因表达的分子机制。阿皮西丁诱导p21(WAF1/Cip1)mRNA的产生不依赖于从头合成蛋白质,并通过位于相对于转录起始位点-82和-77的Sp1-3位点激活p21(WAF1/Cip1)启动子。这种转录激活似乎是由蛋白激酶C(PKC)介导的,因为PKC抑制剂钙泊三醇C显著减弱了通过Sp1位点对p21(WAF1/Cip1)启动子的激活,这伴随着阿皮西丁诱导的p21(WAF1/Cip1)mRNA和蛋白质表达的明显抑制。与阿皮西丁对p21(WAF1/Cip1)启动子的转录激活一致,阿皮西丁处理导致PKCε从胞质部分转移到颗粒部分,而钙泊三醇C预处理可逆转这种转移,表明PKC参与了阿皮西丁通过Sp1位点对p21(WAF1/Cip1)的转录激活。然而,阿皮西丁通过PKC介导的p21(WAF1/Cip1)转录激活似乎独立于组蛋白高度乙酰化,因为阿皮西丁诱导的组蛋白高度乙酰化不受钙泊三醇C的影响。此外,PKC激活剂佛波酯12,13-二丁酸单独诱导p21(WAF1/Cip1)启动子的转录激活、p21(WAF1/Cip1)mRNA和蛋白质表达,而不诱导组蛋白高度乙酰化,这表明阿皮西丁对p21(WAF1/Cip1)的转录激活可能是通过组蛋白高度乙酰化以外的染色质重塑机制介导的。综上所述,这些结果表明PKC信号通路在阿皮西丁对p21(WAF1/Cip1)基因的转录激活中起关键作用。

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