Rhee S, Han Z j, Liu K, Miles H T, Davies D R
Laboratory of Molecular Biology, NIDDK, National Institutes of Health, Bethesda, Maryland 20892, USA.
Biochemistry. 1999 Dec 21;38(51):16810-5. doi: 10.1021/bi991811m.
Extended purine sequences on a DNA strand can lead to the formation of triplex DNA in which the third strand runs parallel to the purine strand. Triplex DNA structures have been proposed to play a role in gene expression and recombination and also have potential application as antisense inhibitors of gene expression. Triplex structures have been studied in solution by NMR, but have hitherto resisted attempts at crystallization. Here, we report a novel design of DNA sequences, which allows the first crystallographic study of DNA segment containing triplexes and its junction with a duplex. In the 1.8 A resolution structure, the sugar-phosphate backbone of the third strand is parallel to the purine-rich strand. The bases of the third strand associate with the Watson and Crick duplex via Hoogsteen-type interactions, resulting in three consecutive C(+).GC, BU.ABU (BU = 5-bromouracil), and C(+).GC triplets. The overall conformation of the DNA triplex has some similarity to the B-form, but is distinct from both A- and B-forms. There are large changes in the phosphate backbone torsion angles (particularly gamma) of the purine strand, probably due to the electrostatic interactions between the phosphate groups and the protonated cytosine. These changes narrow the minor groove width of the purine-Hoogsteen strands and may represent sequence-specific structural variations of the DNA triplex.
DNA链上的延伸嘌呤序列可导致三链DNA的形成,其中第三条链与嘌呤链平行。有人提出三链DNA结构在基因表达和重组中起作用,并且作为基因表达的反义抑制剂也有潜在应用。三链结构已通过核磁共振在溶液中进行研究,但迄今为止结晶尝试均未成功。在此,我们报告了一种新型的DNA序列设计,它使得对包含三链体及其与双链体连接处的DNA片段进行首次晶体学研究成为可能。在分辨率为1.8埃的结构中,第三条链的糖磷酸骨架与富含嘌呤的链平行。第三条链的碱基通过Hoogsteen型相互作用与沃森-克里克双链体结合,形成三个连续的C(+)·GC、BU·ABU(BU = 5-溴尿嘧啶)和C(+)·GC三联体。DNA三链体的整体构象与B型有一些相似之处,但与A型和B型均不同。嘌呤链的磷酸骨架扭转角(特别是γ角)有很大变化,这可能是由于磷酸基团与质子化胞嘧啶之间的静电相互作用所致。这些变化使嘌呤-Hoogsteen链的小沟宽度变窄,可能代表了DNA三链体的序列特异性结构变异。