Stefanovsky V Y, Bazett-Jones D P, Pelletier G, Moss T
Departement de Biochimie et Centre de Recherche en Cancérologie de l'Université Laval (CRCUL), Hôtel-Dieu de Québec, Canada.
Nucleic Acids Res. 1996 Aug 15;24(16):3208-15. doi: 10.1093/nar/24.16.3208.
The formation of a near complete loop of DNA is a striking property of the architectural HMG-box factor xUBF. Here we show that DNA looping only requires a dimer of Nbox13, a C-terminal truncation mutant of xUBF containing just HMG-boxes 1-3. This segment of xUBF corresponds to that minimally required for activation of polymerase I transcription and is sufficient to generate the major characteristics of the footprint given by intact xUBF. Stepwise reduction in the number of HMG-boxes to less than three significantly diminishes DNA bending and provides an estimate of bend angle for each HMG-box. Together the data indicate that a 350 +/- 16 degree loop in 142 +/- 30 bp of DNA can be induced by binding of the six HMG-boxes in an Nbox13 dimer and that DNA looping is probably achieved by six in-phase bends. The positioning of each HMG-box on the DNA does not predominantly involve DNA sequence recognition and is thus an intrinsic property of xUBF.
DNA形成近乎完整的环是结构型HMG盒因子xUBF的一个显著特性。我们在此表明,DNA环化仅需要Nbox13二聚体,Nbox13是xUBF的C端截短突变体,仅包含HMG盒1 - 3。xUBF的这一区域对应于激活聚合酶I转录所需的最小区域,并且足以产生完整xUBF给出的足迹的主要特征。将HMG盒数量逐步减少至少于三个会显著减少DNA弯曲,并为每个HMG盒提供弯曲角度的估计值。这些数据共同表明,Nbox13二聚体中六个HMG盒的结合可在142 ± 30 bp的DNA中诱导出350 ± 16度的环,并且DNA环化可能是通过六个同相弯曲实现的。每个HMG盒在DNA上的定位并不主要涉及DNA序列识别,因此是xUBF的固有特性。