首页> 美国卫生研究院文献>Journal of Virology >Note: The Human T-Cell Leukemia Virus Type 1 Oncoprotein Tax Inhibits the Transcriptional Activity of c-Myb through Competition for the CREB Binding Protein
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Note: The Human T-Cell Leukemia Virus Type 1 Oncoprotein Tax Inhibits the Transcriptional Activity of c-Myb through Competition for the CREB Binding Protein

机译:注意:人类T细胞白血病病毒1型癌蛋白税通过竞争CREB结合蛋白来抑制c-Myb的转录活性

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摘要

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.
机译:强烈要求激活HTLV-1转录,需要使用Tax(一种人类T细胞白血病病毒1型(HTLV-1)的转化蛋白)。这种激活是通过与细胞共激活剂CREB结合蛋白(CBP)的KIX域相互作用而介导的。在这项研究中,我们研究了Tax-KIX相互作用可能在体内介导对细胞基因转录的影响的可能性,因为越来越多的细胞转录因子已显示利用CBP作为共激活因子。由于Tax和c-Myb均与CBP的KIX域相互作用,因此我们测试了Tax解除细胞转录因子c-Myb活性的能力。我们的结果表明,在体内,Tax拮抗c-Myb的转录活性,相反,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,表明这两个转录因子以互斥的方式结合CBP。 Tax的这种新的转录干扰机制可能会促进HTLV-1感染的细胞中全局失调的细胞基因表达,可能导致白血病的发生。

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