Kaushik Mahima, Bansal Aparna, Saxena Sarika, Kukreti Shrikant
Nucleic Acids Research Lab, Department of Chemistry, University of Delhi, (North Campus), Delhi 110007, India.
Biochemistry. 2007 Jun 19;46(24):7119-31. doi: 10.1021/bi0621009. Epub 2007 May 25.
Under physiological concentrations of Na+ and K+, human telomeric DNA can self-associate into G-quadruplexes. On the basis of circular dichroism, gel electrophoresis, gel filtration, and UV-melting experiments, we report here that the double repeat of human telomere (d-TTAGGGTTAGGG; HUM2) forms parallel as well as antiparallel quadruplexes in the presence of K+, whereas Na+ facilitates only the antiparallel form. Here, the gel techniques and CD studies have proved to be complementary in detecting the molecularity and pattern of strand orientation. By correlating the gel and CD experiments, the antiparallel G-quadruplex was identified as a tetrameric species, whereas the parallel G-quadruplex was found to be dimeric. Both structural species were separated through gel filtration, which when run on native polyacrylamide gel electrphoresis (PAGE), confirmed their molecularity. UV-melting profiles also confirm the presence of two biphasic and one monophasic structural species in the presence of K+ and Na+, respectively. Though our observation is consistent with the recent NMR report (Phan, A. T., and Patel, D. J. (2003) J. Am. Chem. Soc. 125, 15021-15027), it seems to differ in terms of the molecularity of the antiparallel quadruplex. A model is proposed for an antiparallel tetrameric quadruplex, showing the possibility of Watson-Crick hydrogen bonds between intervening bases on antiparallel strands. This article expands the known structural motifs of DNA quadruplexes. To the best of our knowledge, four-stranded antiparallel quadruplexes have not been characterized to date. On the basis of the model, we hypothesize a possible mechanism for telomere-telomere association involving their G-overhangs, during certain stages of the cell cycle. The knowledge of peculiar geometries of the G-quadruplexes may also have implications for its specific recognition by ligands.
在生理浓度的Na⁺和K⁺条件下,人类端粒DNA可自行缔合形成G-四链体。基于圆二色性、凝胶电泳、凝胶过滤和紫外熔解实验,我们在此报告,人类端粒的双重复序列(d-TTAGGGTTAGGG;HUM2)在K⁺存在时可形成平行和反平行四链体,而Na⁺仅促进反平行形式的形成。在此,凝胶技术和圆二色性研究已被证明在检测链取向的分子性和模式方面具有互补性。通过关联凝胶和圆二色性实验,反平行G-四链体被鉴定为四聚体物种,而平行G-四链体被发现为二聚体。两种结构物种通过凝胶过滤分离,当在天然聚丙烯酰胺凝胶电泳(PAGE)上运行时,证实了它们的分子性。紫外熔解曲线也分别证实了在K⁺和Na⁺存在时存在两种双相和一种单相结构物种。尽管我们的观察结果与最近的核磁共振报告(Phan, A. T., and Patel, D. J. (2003) J. Am. Chem. Soc. 125, 15021 - 15027)一致,但在反平行四链体的分子性方面似乎有所不同。提出了一个反平行四聚体四链体的模型,显示了反平行链上间隔碱基之间形成沃森-克里克氢键的可能性。本文扩展了已知的DNA四链体结构基序。据我们所知,四链反平行四链体迄今为止尚未得到表征。基于该模型,我们假设了在细胞周期的某些阶段,涉及端粒G-悬垂的端粒-端粒缔合的可能机制。G-四链体特殊几何形状的知识也可能对其被配体特异性识别有影响。