Hurst H C, Jones N C
Gene Regulation Group, Imperial Cancer Research Fund, London, England.
Genes Dev. 1987 Dec;1(10):1132-46. doi: 10.1101/gad.1.10.1132.
We have investigated the E1A-inducible E3 promoter of adenovirus type 5 with respect to its ability to bind specific nuclear proteins. Four distinct nucleoprotein-binding sites were detected, located between positions-7 to -33, -44 to -68, -81 to -103, and -154 to -183, relative to the E3 cap site. These sites contain sequences previously shown to be functionally important for efficient E3 transcription. No major qualitative or quantitative differences were found in the binding pattern between nucleoprotein extracts prepared from uninfected or adenovirus-infected HeLa cells. Competition experiments suggest that the factors binding to the -154 to -183 and -81 to -103 sites are the previously identified nucleoproteins, NF1 and AP1, respectively. The factor binding to the -44 to -68 site, which we term ATF, also interacts with other E1A-inducible promoters and is very similar and probably identical to the factor that binds to the cAMP-responsive element of somatostatin. We have purified this factor, which is a protein of 43 kD in size.
我们研究了5型腺病毒E1A诱导型E3启动子结合特异性核蛋白的能力。检测到四个不同的核蛋白结合位点,相对于E3帽位点,分别位于-7至-33、-44至-68、-81至-103和-154至-183位。这些位点包含先前已证明对高效E3转录具有功能重要性的序列。在未感染或腺病毒感染的HeLa细胞制备的核蛋白提取物的结合模式中,未发现主要的定性或定量差异。竞争实验表明,结合到-154至-183和-81至-103位点的因子分别是先前鉴定的核蛋白NF1和AP1。结合到-44至-68位点的因子,我们称之为ATF,也与其他E1A诱导型启动子相互作用,并且与结合生长抑素cAMP反应元件的因子非常相似,可能相同。我们已经纯化了这个因子,它是一种大小为43 kD的蛋白质。