Bresnahan W A, Albrecht T, Thompson E A
Departments of Human Biological Chemistry and Genetics, University of Texas Medical Branch, Galveston, Texas 77555-0645, USA.
J Biol Chem. 1998 Aug 21;273(34):22075-82. doi: 10.1074/jbc.273.34.22075.
Human cytomegalovirus (HCMV) activates cyclin E/Cdk2, which regulates cell cycle progression in G1 and S phase of the cell cycle. HCMV activation of cyclin E/Cdk2 can be demonstrated in cells that are refractory to normal mitotic stimuli. This observation suggests that the virus has some means to overcome the stringent control on expression of cell cycle progression factors that is characteristic of cells in the G0 state. One of the mechanisms involved in activation of cyclin E/Cdk2 is the induction of cyclin E expression. We report here that HCMV induces cyclin E expression through a transcriptional mechanism. The cyclin E gene is activated by the HCMV 86-kDa immediate early gene product (IE86), which directly binds to nucleotide sequences within the cyclin E promoter. An IE86 DNA-binding mutant neither binds nor activates the cyclin E promoter. IE86-binding sites within the cyclin E promoter are required for IE86-mediated activation, and deletion of the IE86-binding site inhibits IE86 activation of the cyclin E promoter. We also demonstrate that mutation of the known E2F-binding sites in the cyclin E promoter does not block activation by HCMV or IE86. These data provide a molecular mechanism for HCMV induction of cyclin E and represent the first report of IE86 directly binding to a cellular promoter.
人巨细胞病毒(HCMV)激活细胞周期蛋白E/细胞周期蛋白依赖性激酶2(Cdk2),该激酶调节细胞周期G1期和S期的进程。在对正常有丝分裂刺激无反应的细胞中,可以证明HCMV对细胞周期蛋白E/Cdk2的激活作用。这一观察结果表明,该病毒具有某种方式来克服对处于G0状态细胞所特有的细胞周期进程因子表达的严格控制。细胞周期蛋白E/Cdk2激活所涉及的机制之一是细胞周期蛋白E表达的诱导。我们在此报告,HCMV通过转录机制诱导细胞周期蛋白E表达。细胞周期蛋白E基因由HCMV 86 kDa的立即早期基因产物(IE86)激活,该产物直接与细胞周期蛋白E启动子内的核苷酸序列结合。IE86 DNA结合突变体既不结合也不激活细胞周期蛋白E启动子。细胞周期蛋白E启动子内的IE86结合位点是IE86介导激活所必需的,缺失IE86结合位点会抑制IE86对细胞周期蛋白E启动子的激活。我们还证明,细胞周期蛋白E启动子中已知的E2F结合位点的突变不会阻断HCMV或IE86的激活。这些数据为HCMV诱导细胞周期蛋白E提供了一种分子机制,并且是IE86直接结合细胞启动子的首次报道。