Gaston K, Fried M
Eukaryotic Gene Organisation and Expression Laboratory, Imperial Cancer Research Fund, London, UK.
Nucleic Acids Res. 1992 Dec 11;20(23):6297-301. doi: 10.1093/nar/20.23.6297.
The Surf-1/Surf-2 bi-directional promoter contains binding sites for at least three transcription factors (Su1, Su2, and Su3). By screening a lambda gt11 HeLa cell cDNA expression library with a concatenated Su2 factor binding site, we isolated a cDNA which encodes a protein with sequence-specific DNA binding activity. Gel retardation assays showed that the cloned factor binds specifically to the Su2 factor binding site present in the human Surf-1/Surf-2 promoter but not to an Su2 site containing mutated base pairs. Co-transfection experiments demonstrated that the cloned cDNA had little or no effect on the expression of a reporter gene under the control of multiple Su2 factor binding sites. Similarly a fusion protein in which the acidic activation domain of HSV VP16 was linked to the cloned factor had no effect, implying that the factor does not function as a DNA binding protein in vivo. DNA sequence analysis revealed that the cloned cDNA is identical to that of human steroid 5 alpha-reductase 1, an enzyme which converts testosterone to dihydrotestosterone. These results are discussed with respect to other putative transcription factors which have been isolated from cDNA expression libraries on the basis of their sequence-specific DNA binding activity.
Surf-1/Surf-2双向启动子含有至少三种转录因子(Su1、Su2和Su3)的结合位点。通过用串联的Su2因子结合位点筛选λgt11 HeLa细胞cDNA表达文库,我们分离出一个编码具有序列特异性DNA结合活性蛋白质的cDNA。凝胶阻滞分析表明,克隆的因子特异性结合人Surf-1/Surf-2启动子中存在的Su2因子结合位点,但不结合含有突变碱基对的Su2位点。共转染实验表明,克隆的cDNA对多个Su2因子结合位点控制下的报告基因表达几乎没有影响。同样,一种融合蛋白(其中HSV VP16的酸性激活结构域与克隆的因子相连)也没有影响,这意味着该因子在体内不作为DNA结合蛋白发挥作用。DNA序列分析表明,克隆的cDNA与人类类固醇5α-还原酶1相同,该酶将睾酮转化为二氢睾酮。结合其他基于序列特异性DNA结合活性从cDNA表达文库中分离出的假定转录因子对这些结果进行了讨论。