Uittenbogaard M N, Armstrong A P, Chiaramello A, Nyborg J K
Department of Microbiology, Colorado State University, Fort Collins 80523.
J Biol Chem. 1994 Sep 9;269(36):22466-9.
The human T-cell leukemia virus type I (HTLV-I) oncoprotein Tax is a potent activator of viral and cellular gene transcription. Tax does not bind DNA directly but utilizes cellular transcription factors to mediate activation. In this report, we examine the role of the basic helix-loop-helix (bHLH) proteins in Tax deregulation of gene expression, as these proteins play a critical role in progression through the cell cycle and have been implicated in neoplastic disease. We show that the bHLH proteins do not mediate activation, but instead mediate repression of gene expression in the presence of Tax. We further show that a consensus bHLH binding site in the promoter of the beta-polymerase gene, which encodes an enzyme involved in DNA repair, mediates the previously reported repression of beta-polymerase gene expression by Tax. Together, these results suggest that Tax may induce malignant transformation, at least in part, through bHLH-mediated repression of key cellular regulatory genes.
人类I型T细胞白血病病毒(HTLV-I)癌蛋白Tax是病毒和细胞基因转录的强效激活剂。Tax不直接结合DNA,而是利用细胞转录因子来介导激活。在本报告中,我们研究了碱性螺旋-环-螺旋(bHLH)蛋白在Tax对基因表达的失调中的作用,因为这些蛋白在细胞周期进程中起关键作用,并且与肿瘤疾病有关。我们表明,bHLH蛋白不介导激活,而是在有Tax存在的情况下介导基因表达的抑制。我们进一步表明,β-聚合酶基因启动子中的一个共有bHLH结合位点介导了先前报道的Tax对β-聚合酶基因表达的抑制,该基因编码一种参与DNA修复的酶。总之,这些结果表明,Tax可能至少部分地通过bHLH介导的对关键细胞调节基因的抑制来诱导恶性转化。