Phan Anh Tuân, Modi Yasha S, Patel Dinshaw J
Structural Biology Program, Memorial Sloan-Kettering Cancer Center, New York, New York 10021, USA.
J Am Chem Soc. 2004 Jul 21;126(28):8710-6. doi: 10.1021/ja048805k.
The nuclease-hypersensitivity element III1 in the c-myc promoter is a good anticancer target since it largely controls transcriptional activation of the important c-myc oncogene. Recently, the guanine-rich strand of this element has been shown to form an equilibrium between G-quadruplex structures built from two different sets of G-stretches; two models of intramolecular fold-back antiparallel-stranded G-quadruplexes, called "basket" and "chair" forms, were proposed. Here, we show by NMR that two sequences containing these two sets of G-stretches form intramolecular propeller-type parallel-stranded G-quadruplexes in K(+)-containing solution. The two structures involve a core of three stacked G-tetrads formed by four parallel G-stretches with all anti guanines and three double-chain-reversal loops bridging three G-tetrad layers. The central loop contains two or six residues, while the two other loops contain only one residue.
c-myc启动子中的核酸酶超敏元件III1是一个很好的抗癌靶点,因为它在很大程度上控制着重要的c-myc癌基因的转录激活。最近,该元件富含鸟嘌呤的链已被证明在由两组不同的G-序列形成的G-四链体结构之间形成平衡;提出了两种分子内折叠反向反平行链G-四链体模型,即“篮状”和“椅状”形式。在这里,我们通过核磁共振表明,包含这两组G-序列的两个序列在含K(+)的溶液中形成分子内螺旋桨型平行链G-四链体。这两种结构都包含一个由四个平行G-序列形成的三个堆叠G-四联体核心,所有鸟嘌呤均为反式构象,以及三个双链反向环,它们桥接三个G-四联体层。中央环包含两个或六个残基,而另外两个环仅包含一个残基。