Natesan S, Gilman M
Cold Spring Harbor Laboratory, Cold Spring Harbor, New York 11724, USA.
Mol Cell Biol. 1995 Nov;15(11):5975-82. doi: 10.1128/MCB.15.11.5975.
YY1 is a multifunctional transcription factor that acts as an activator or repressor in different contexts. YY1 binds to multiple sites in the mouse c-fos promoter, inducing at each site a sharp DNA bend. Binding of YY1 to a site situated between the cyclic AMP response element (CRE) and the TATA box bends the DNA in a way that interferes with the interaction of proteins bound at the CRE and TATA elements, resulting in repression of transcription. Here, we show that binding of YY1 to a different site in the c-fos promoter has a different result. Binding of YY1 to the c-fos serum response element (SRE) enhances the binding of serum response factor (SRF). This enhancement requires the binding of YY1 to SRE DNA. YY1 and SRF can cooccupy the SRE at least transiently. In the region of overlapping contact, YY1 contacts DNA in the major groove, while SRF contacts DNA in the minor groove. YY1 also enhances the association of SRF with the SRE in transfected insect cells. Thus, although YY1 induces similar structural changes in DNA at different binding sites, it can have distinct local effects on protein-DNA and protein-protein interactions. These data support a general role for YY1 in the building of highly organized promoter complexes.
YY1是一种多功能转录因子,在不同情况下可作为激活剂或抑制剂发挥作用。YY1与小鼠c-fos启动子中的多个位点结合,在每个位点诱导DNA发生急剧弯曲。YY1与位于环磷酸腺苷反应元件(CRE)和TATA盒之间的一个位点结合,会使DNA弯曲,从而干扰结合在CRE和TATA元件上的蛋白质之间的相互作用,导致转录受到抑制。在此,我们表明YY1与c-fos启动子中不同位点的结合会产生不同的结果。YY1与c-fos血清反应元件(SRE)结合可增强血清反应因子(SRF)的结合。这种增强作用需要YY1与SRE DNA结合。YY1和SRF至少可短暂地共同占据SRE。在重叠接触区域,YY1在大沟中与DNA接触,而SRF在小沟中与DNA接触。YY1还可增强转染昆虫细胞中SRF与SRE的结合。因此,尽管YY1在不同结合位点诱导DNA发生相似的结构变化,但它对蛋白质-DNA和蛋白质-蛋白质相互作用可产生不同的局部影响。这些数据支持YY1在构建高度有序的启动子复合物中发挥普遍作用。