Wang Di, Guo Ming-Xiong, Hu Hai-Ming, Zhao Zhou-Zhou, Qiu Hong-Ling, Shao Huan-Jie, Zhu Chen-Gang, Xue Lu, Shi Yun-Bo, Li Wen-Xin
State Key Laboratory of Virology, College of Life Sciences, Wuhan University, Wuhan 430072, China.
J Biol Chem. 2008 Jun 13;283(24):16299-308. doi: 10.1074/jbc.M706426200. Epub 2008 Mar 28.
Expression of the human T-cell leukemia virus type 1 (HTLV-1) oncoprotein Tax is correlated with cellular transformation, contributing to the development of adult T-cell leukemia. In this study, we investigated the role of Tax in the regulation of the ZNF268 gene, which plays a role in the differentiation of blood cells and the pathogenesis of leukemia. We demonstrated that ZNF268 mRNA was repressed in HTLV-1-infected cells. We also showed that stable and transient expression of HTLV-1 Tax led to repression of ZNF268. In addition, by using reporter constructs that bear the human ZNF268 promoter and its mutants, we showed that Tax repressed ZNF268 promoter in a process dependent on a functional cAMP-responsive element. By using Tax, cAMP-responsive element-binding protein (CREB)-1, CREB-2, and their mutants, we further showed that Tax repressed ZNF268 through the CREB/activating transcription factor pathway. Electrophoretic mobility shift assays and chromatin immunoprecipitation demonstrated the formation of the complex of Tax.CREB-1 directly at the cAMP-responsive element both in vitro and in vivo. These findings suggest a role for ZNF268 in aberrant T-cell proliferation observed in HTLV-1-associated diseases.
人类嗜T细胞病毒1型(HTLV-1)癌蛋白Tax的表达与细胞转化相关,促进成人T细胞白血病的发展。在本研究中,我们调查了Tax在ZNF268基因调控中的作用,该基因在血细胞分化和白血病发病机制中发挥作用。我们证明ZNF268 mRNA在HTLV-1感染的细胞中受到抑制。我们还表明,HTLV-1 Tax的稳定和瞬时表达导致ZNF268的抑制。此外,通过使用携带人类ZNF268启动子及其突变体的报告构建体,我们表明Tax在依赖功能性cAMP反应元件的过程中抑制ZNF268启动子。通过使用Tax、cAMP反应元件结合蛋白(CREB)-1、CREB-2及其突变体,我们进一步表明Tax通过CREB/激活转录因子途径抑制ZNF268。电泳迁移率变动分析和染色质免疫沉淀证明Tax.CREB-1复合物在体外和体内直接在cAMP反应元件处形成。这些发现提示ZNF268在HTLV-1相关疾病中观察到的异常T细胞增殖中发挥作用。