Kan Lou-sing, Pasternack Laura, Wey Ming-Tsair, Tseng Yu-Yu, Huang Dee-Hua
Institute of Chemistry, Academia Sinica, Taipei, Taiwan 11529.
Biophys J. 2006 Oct 1;91(7):2552-63. doi: 10.1529/biophysj.106.084137. Epub 2006 Jul 7.
In this study, we investigate the role of the apex nucleotides of the two turns found in the intramolecular "paperclip" type triplex DNA formed by 5'-TCTCTCCTCTCTAGAGAG-3'. Our previously published structure calculations show that residues C7-A18 form a hairpin turn via Watson-Crick basepairing and residues T1-C6 bind into the major groove of the hairpin via Hoogsteen basepairing resulting in a broad turn of the T1-T12 5'-pyrimidine section of the DNA. We find that only the C6C7/G18 apex triad (and not the T12A13/T1 apex triad) is required for intramolecular triplex formation, is base independent, and occurs whether the purine section is located at the 5' or 3' end of the sequence. NMR spectroscopy and molecular dynamics simulations are used to investigate a bimolecular complex (which retains only the C6C7/G18 apex) in which a pyrimidine strand 5'- TCTCTCCTCTCT-3' makes a broad fold stabilized by the purine strand 5'-AGAGAG-3' via Watson Crick pairing to the T8-T12 and Hoogsteen basepairing to T1-T5 of the pyrimidine strand. Interestingly, this investigation shows that this 5'-AGAGAG-3' oligo acts as a new kind of triplex forming oligonucleotide, and adds to the growing number of triplex forming oligonucleotides that may prove useful as therapeutic agents.
在本研究中,我们研究了由5'-TCTCTCCTCTCTAGAGAG-3'形成的分子内“回形针”型三链体DNA中发现的两个转角处的顶端核苷酸的作用。我们之前发表的结构计算表明,残基C7 - A18通过沃森-克里克碱基配对形成发夹转角,残基T1 - C6通过 hoogsteen 碱基配对结合到发夹的大沟中,导致DNA的T1 - T12 5'-嘧啶部分形成一个宽转角。我们发现,分子内三链体形成仅需要C6C7/G18顶端三联体(而不是T12A13/T1顶端三联体),它不依赖于碱基,并且无论嘌呤部分位于序列的5'端还是3'端都会发生。核磁共振光谱和分子动力学模拟用于研究一个双分子复合物(仅保留C6C7/G18顶端),其中嘧啶链5'-TCTCTCCTCTCT-3'通过与嘌呤链5'-AGAGAG-3'的沃森-克里克配对与嘧啶链的T8 - T12以及 hoogsteen 碱基配对与T1 - T5形成一个宽折叠结构。有趣的是,这项研究表明,这种5'-AGAGAG-3'寡核苷酸作为一种新型的三链体形成寡核苷酸,增加了可能被证明作为治疗剂有用的三链体形成寡核苷酸的数量。