Dikstein R, Faktor O, Shaul Y
Department of Molecular Genetics and Virology, Weizmann Institute of Science, Rehovot, Israel.
Mol Cell Biol. 1990 Aug;10(8):4427-30. doi: 10.1128/mcb.10.8.4427-4430.1990.
We used the enhancer-binding protein C/EBP as a model to study the nature and the complexity of interaction of an enhancer-binding protein with its target DNA. We found that bacterially expressed C/EBP binds the hepatitis B virus enhancer at multiple sites in a hierarchic and cooperative manner. At low concentrations, only the E element is occupied, but at higher concentrations, additional sites are filled including a site that binds EP, a crucial enhancer-activating protein. This pattern of C/EBP binding may explain the concentration-dependent effect of C/EBP on enhancer activity.
我们以增强子结合蛋白C/EBP作为模型,来研究增强子结合蛋白与其靶DNA相互作用的性质和复杂性。我们发现,细菌表达的C/EBP以分级协同的方式在多个位点结合乙型肝炎病毒增强子。在低浓度时,只有E元件被占据,但在较高浓度时,其他位点也会被占据,包括一个与关键增强子激活蛋白EP结合的位点。C/EBP的这种结合模式可能解释了C/EBP对增强子活性的浓度依赖性效应。