Houbaviy H B, Usheva A, Shenk T, Burley S K
Laboratory of Molecular Biophysics, Rockefeller University, New York, NY 10021-6399, USA.
Proc Natl Acad Sci U S A. 1996 Nov 26;93(24):13577-82. doi: 10.1073/pnas.93.24.13577.
Ying-Yang 1 protein (YY1) supports specific, unidirectional initiation of messenger RNA production by RNA polymerase II from two adjacent start sites in the adeno-associated virus P5 promoter, a process which is independent of the TATA box-binding protein (TBP). The 2.5-A resolution YY1-initiator element cocrystal structure reveals four zinc fingers recognizing a YY1-binding consensus sequence. Upstream of the transcription start sites protein-DNA contacts involve both strands and downstream they are virtually restricted to the template strand, permitting access to the active center of RNA polymerase II and ensuring specificity and directionality. The observed pattern of protein-DNA contacts also explains YY1 binding to a preformed transcription bubble, and YY1 binding to a DNA/RNA hybrid analog of the P5 promoter region containing a nascent RNA transcript. A model is proposed for YY1-directed, TBP-independent transcription initiation.
阴阳1蛋白(YY1)支持RNA聚合酶II从腺相关病毒P5启动子中的两个相邻起始位点特异性、单向地起始信使RNA的产生,这一过程独立于TATA盒结合蛋白(TBP)。分辨率为2.5埃的YY1-起始子元件共晶体结构揭示了四个锌指识别YY1结合共有序列。在转录起始位点上游,蛋白质与DNA的接触涉及两条链,而在下游,它们实际上仅限于模板链,从而允许接近RNA聚合酶II的活性中心并确保特异性和方向性。观察到的蛋白质与DNA接触模式也解释了YY1与预先形成的转录泡的结合,以及YY1与包含新生RNA转录本的P5启动子区域的DNA/RNA杂交类似物的结合。提出了一个YY1指导的、不依赖TBP的转录起始模型。