Semmes O J, Jeang K T
Molecular Virology Section, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland 20892.
J Virol. 1995 Mar;69(3):1827-33. doi: 10.1128/JVI.69.3.1827-1833.1995.
Fourteen mutants were used to delineate a minimal activation domain in the Tax protein of human T-cell leukemia virus type I. In an assay using a Gal4-Tax (GalTx) fusion protein and a responsive promoter containing Gal4 consensus binding sites, we found that activation was "squelched" by coexpression of wild-type Tax protein in trans. When Tax mutants were tested for squelching, many competed effectively against GalTx. However, those containing changes in amino acids 289 to 322 failed to inhibit activity. In particular, three mutants that were expressed stably, with changes at amino acids 289, 296, and 320 respectively, did not squelch GalTx activity. On the other hand, mutants with individual changes at amino acid 3, 9, 29, 41, 273, and 337 efficiently inhibited GalTx function. Three other mutants failed to be stably expressed. In separate experiments, when fused alone to the DNA-binding domain of Gal4, amino acids 289 to 322 of Tax conferred trans activation ability. This fusion protein was able to activate a core promoter. These findings suggest that amino acids 289 to 322 define a region that contacts an essential transcription factor and that this region is a modular activation domain.
利用14种突变体来确定I型人类T细胞白血病病毒Tax蛋白中的最小激活结构域。在一项使用Gal4-Tax(GalTx)融合蛋白和含有Gal4共有结合位点的反应性启动子的检测中,我们发现反式共表达野生型Tax蛋白会使激活作用“被抑制”。当检测Tax突变体的抑制作用时,许多突变体能够有效地与GalTx竞争。然而,那些在氨基酸289至322处发生变化的突变体无法抑制活性。特别是,分别在氨基酸289、296和320处发生变化且稳定表达的三个突变体,并未抑制GalTx活性。另一方面,在氨基酸3、9、29、41、273和337处发生单个变化的突变体能够有效抑制GalTx功能。另外三个突变体未能稳定表达。在单独的实验中,当Tax的氨基酸289至322单独与Gal4的DNA结合结构域融合时,赋予了反式激活能力。这种融合蛋白能够激活核心启动子。这些发现表明,氨基酸289至322定义了一个与必需转录因子接触的区域,并且该区域是一个模块化激活结构域。