Reddy T R, Tang H, Li X, Wong-Staal F
Department of Medicine, University of California San Diego, La Jolla 92093-0665, USA.
Oncogene. 1997 Jun 12;14(23):2785-92. doi: 10.1038/sj.onc.1201119.
The Tax protein of the Human T-cell Leukemia Virus (HTLV) activates the expression of viral mRNA through a three 21 bp repeat enhancer located within the HTLV-1 LTR. Since Tax does not bind to the 21 bp DNA repeats directly, it has been speculated that Tax interacts with cellular protein(s) which mediate binding to the enhancer. We employed the yeast two hybrid system to identify host proteins that are potentially relevant to Tax transactivation. We identified a Tax binding protein encoded from a cDNA expression library derived from peripheral blood lymphocytes. The corresponding cDNA has sequence identity with a known transcription factor, activating factor-4 (ATF-4). ATF-4 also binds to GST-Tax fusion protein in vitro. Tax mutants that did not transactivate the HTLV-1 LTR also failed to bind ATF-4. The critical domain for Tax binding resides in a 85 amino acid stretch in the C-terminus of ATF-4, which contains the basic domain and leucine zipper. We further demonstrated that both full length and N-terminal truncated ATF-4 were able to enhance Tax transactivation. Thus, ATF-4 may act as an adapter between Tax and the TRE (Tax responsive element), and play an important role in Tax-mediated transactivation.
人类T细胞白血病病毒(HTLV)的Tax蛋白通过位于HTLV-1长末端重复序列(LTR)内的三个21碱基对重复增强子来激活病毒mRNA的表达。由于Tax并不直接与21碱基对的DNA重复序列结合,因此推测Tax与介导结合增强子的细胞蛋白相互作用。我们利用酵母双杂交系统来鉴定可能与Tax反式激活相关的宿主蛋白。我们从外周血淋巴细胞来源的cDNA表达文库中鉴定出一种Tax结合蛋白。相应的cDNA与已知转录因子激活因子-4(ATF-4)具有序列同源性。ATF-4在体外也能与GST-Tax融合蛋白结合。不能反式激活HTLV-1 LTR的Tax突变体也不能与ATF-4结合。Tax结合的关键结构域位于ATF-4 C末端的85个氨基酸片段中,该片段包含碱性结构域和亮氨酸拉链。我们进一步证明全长和N末端截短的ATF-4都能够增强Tax的反式激活作用。因此,ATF-4可能作为Tax与Tax反应元件(TRE)之间的衔接蛋白,并在Tax介导的反式激活中发挥重要作用。