Colgin M A, Nyborg J K
Department of Biochemistry and Molecular Biology, Colorado State University, Fort Collins, Colorado 80523-1870, USA.
J Virol. 1998 Nov;72(11):9396-9. doi: 10.1128/JVI.72.11.9396-9399.1998.
Tax, the transforming protein of human T-cell leukemia virus type 1 (HTLV-1), is required for strong activation of HTLV-1 transcription. This activation is mediated through interaction with the KIX domain of the cellular coactivator CREB binding protein (CBP). In this study we examined the possibility that the Tax-KIX interaction may mediate effects on cellular gene transcription in vivo, as a growing number of cellular transcription factors have been shown to utilize CBP as a coactivator. We tested the ability of Tax to deregulate the activity of the cellular transcription factor, c-Myb, since both Tax and c-Myb interact with the KIX domain of CBP. Our results show that in vivo, Tax antagonizes the transcriptional activity of c-Myb and, reciprocally, c-Myb antagonizes the transcriptional activity of Tax. Furthermore, c-Myb competes for KIX binding to Tax in vitro, indicating that these two transcription factors bind CBP in a mutually exclusive manner. This novel mechanism of transcriptional interference by Tax may promote globally deregulated cellular gene expression in the HTLV-1-infected cell, possibly leading to leukemogenesis.
Tax是人类1型T细胞白血病病毒(HTLV-1)的转化蛋白,是HTLV-1转录强烈激活所必需的。这种激活是通过与细胞共激活因子CREB结合蛋白(CBP)的KIX结构域相互作用介导的。在本研究中,我们探讨了Tax-KIX相互作用可能在体内介导对细胞基因转录影响的可能性,因为越来越多的细胞转录因子已被证明利用CBP作为共激活因子。我们测试了Tax解除细胞转录因子c-Myb活性调控的能力,因为Tax和c-Myb都与CBP的KIX结构域相互作用。我们的结果表明,在体内,Tax拮抗c-Myb的转录活性,反之,c-Myb拮抗Tax的转录活性。此外,c-Myb在体外竞争KIX与Tax的结合,表明这两种转录因子以互斥的方式结合CBP。Tax这种新的转录干扰机制可能会促进HTLV-1感染细胞中整体失控的细胞基因表达,可能导致白血病发生。