Fujii M, Chuhjo T, Minamino T, Masaaki N, Miyamoto K, Seiki M
Department of Molecular Virology and Oncology, Kanazawa University, Ishikawa, Japan.
Oncogene. 1995 Jul 6;11(1):7-14.
Tax of human T-cell leukemia virus type I (HTLV-I) activates transcription at a CArG box of various immediate early genes such as the proto-oncogene c-fos. To do this, Tax does not directly bind to the CArG box, but instead binds to the CArG binding factor SRF. In this study, we investigated the domain of SRF required for the activation by Tax and studied the role of this domain on transcriptional regulation at the CArG box. Using a fusion protein of SRF with a yeast transcription factor GAL4, the 14 amino acid (aa) portion (aa 422-435) of SRF was identified as the domain required for Tax activation [Tax-responsive region of SRF (TRRS)]. By means of a two hybrid system, we showed that TRRS was essential for the interaction of SRF with Tax in vivo. The over-expression of SRF with a deletion of TRRS inhibited the Tax activation at the CArG box. Thus, TRRS is the domain of SRF that is essential for Tax activation at the CArG box. Unlike to Tax activation, TRRS was not required for TPA (12-o-tetradecanoylphobol-13-acetate) induction at the CArG box, but a TRRS deletion enhanced the basal activity at the CArG box both under serum-starved and TPA-stimulated conditions. These results suggest that TRRS negatively regulates the transcriptional activation function of SRF, and consequently contributes to the low basal activity at the CArG box before TPA induction.
人类嗜T淋巴细胞病毒I型(HTLV-I)的Tax蛋白可激活多种即早基因(如原癌基因c-fos)的CArG框处的转录。为此,Tax蛋白并不直接结合CArG框,而是与CArG结合因子血清反应因子(SRF)结合。在本研究中,我们研究了Tax蛋白激活所需的SRF结构域,并探讨了该结构域在CArG框转录调控中的作用。利用SRF与酵母转录因子GAL4的融合蛋白,确定了SRF的14个氨基酸(aa)部分(aa 422-435)为Tax蛋白激活所需的结构域[SRF的Tax反应区域(TRRS)]。通过双杂交系统,我们证明TRRS在体内对SRF与Tax蛋白的相互作用至关重要。缺失TRRS的SRF过表达抑制了CArG框处的Tax蛋白激活。因此,TRRS是SRF在CArG框处Tax蛋白激活所必需的结构域。与Tax蛋白激活不同,TRRS在CArG框处的佛波酯(TPA,12-O-十四酰佛波醇-13-乙酸酯)诱导中并非必需,但在血清饥饿和TPA刺激条件下,TRRS缺失均增强了CArG框处的基础活性。这些结果表明,TRRS对SRF的转录激活功能起负调控作用,因此在TPA诱导前有助于CArG框处的低基础活性。