Boros I M, Tie F, Giam C Z
Department of Medicine, Case Western Reserve University, Cleveland, Ohio 44106, USA.
Virology. 1995 Dec 1;214(1):207-14. doi: 10.1006/viro.1995.9939.
The bovine leukemia virus transactivator, BLV Tax, augments transcription from three imperfect 21-bp repeats in the viral transcriptional regulatory region. Each BLV 21-bp repeat contains a cAMP response element (CRE) in the center and unique 5' and 3' neighboring sequences which are crucial for the transcriptional activation by BLV Tax. Here we describe the interactions of recombinant BLV Tax with cellular bZip proteins. The recombinant BLV Tax, tagged at the carboxy terminus with a hexahistidine extension, was prepared by solubilization in 6 M guanidine hydrochloride and renaturation on the Ni(2+)-chelating Sepharose gel matrix. The renatured BLV TaxH6 activates the BLV LTR when introduced into HeLa cells by scrape loading. Furthermore, the purified BLV TaxH6 enhances binding of members of the CREB/ATF family of bZip proteins to CRE motifs by interacting with their bZip domains in vitro. Chemical cross-linking indicates that dimerization of bZip proteins such as CREB becomes greatly facilitated in the presence of BLV Tax. These results suggest that BLV Tax interacts directly with CREB/ATF-like factors to activate viral mRNA transcription.
牛白血病病毒反式激活因子BLV Tax可增强病毒转录调控区中三个不完全的21碱基对重复序列的转录。每个BLV 21碱基对重复序列在中心位置包含一个环磷酸腺苷反应元件(CRE)以及独特的5'和3'侧翼序列,这些序列对于BLV Tax的转录激活至关重要。在此,我们描述了重组BLV Tax与细胞碱性亮氨酸拉链(bZip)蛋白的相互作用。在羧基末端带有六组氨酸延伸标签的重组BLV Tax,通过在6 M盐酸胍中溶解并在镍(2+)螯合琼脂糖凝胶基质上复性来制备。当通过刮擦加载法导入HeLa细胞时,复性后的BLV TaxH6可激活BLV长末端重复序列(LTR)。此外,纯化后的BLV TaxH6在体外通过与其bZip结构域相互作用,增强了bZip蛋白CREB/ATF家族成员与CRE基序的结合。化学交联表明,在BLV Tax存在的情况下,CREB等bZip蛋白的二聚化变得更加容易。这些结果表明,BLV Tax直接与CREB/ATF样因子相互作用以激活病毒mRNA转录。