首页> 美国卫生研究院文献>other >Not All G-Quadruplexes are Created Equally: An Investigation of the Structural Polymorphism of the c-Myc G-Quadruplex-Forming Sequence and its Interaction with the Porphyrin meso-Tetra(N-methyl-4-pyridyl)porphine
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Not All G-Quadruplexes are Created Equally: An Investigation of the Structural Polymorphism of the c-Myc G-Quadruplex-Forming Sequence and its Interaction with the Porphyrin meso-Tetra(N-methyl-4-pyridyl)porphine

机译:不是所有的G-四都是一样的:将c-myc的G-四链体形成用序列的结构多态性的调查以及其与卟啉meso-四(N-甲基-4-吡啶基)卟啉的相互作用

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摘要

G-quadruplexes, DNA tertiary structures highly localized to functionally important sites within the human genome, have emerged as important new drug targets. The putative G-quadruplex-forming sequence (Pu27) in the NHE-III1 promoter region of the c-Myc gene is of particular interest as stabilization of this G-quadruplex with TMPyP4 has been shown to repress c-Myc transcription. In this study, we examine the Pu27 G-quadruplex-forming sequence and its interaction with TMPyP4. We report that the Pu27 sequence exists as a heterogeneous mixture of monomeric and higher-order G-quadruplex species in vitro and that this mixture can be partially resolved by size exclusion chromatography (SEC) separation. Within this ensemble of configurations, the equilibrium can be altered by modifying the buffer composition, annealing procedure, and dialysis protocol thereby affecting the distribution of G-quadruplex species formed. TMPyP4 was found to bind preferentially to higher-order G-quadruplex species suggesting the possibility of stabilization of the junctions of the c-Myc G-quadruplex multimers by porphyrin end-stacking. We also examined four modified c-Myc sequences that have been previously reported and found a narrower distribution of quadruplex configurations compared to the parent Pu27 sequence. We could not definitively conclude whether these G-quadruplex structures were selected from the original ensemble or if they are new G-quadruplex structures. Since these sequences differ considerably from the wild-type promoter sequence, it is unclear whether their structures have any actual biological relevance. Additional studies are needed to examine how the polymorphic nature of G-quadruplexes affects the interpretation of in vitro data for c-Myc and other G-quadruplexes. The findings reported here demonstrate that experimental conditions contribute significantly to G-quadruplex formation and should be carefully considered, controlled, and reported in detail.
机译:G-四链体(DNA三级结构高度定位于人类基因组中功能上重要的位点)已成为重要的新药物靶标。 c-Myc基因的NHE-III1启动子区域中假定的G-四链体形成序列(Pu27)特别令人感兴趣,因为已证明用TMPyP4稳定该G-四链体可抑制c-Myc转录。在这项研究中,我们检查了Pu27 G-四链体形成序列及其与TMPyP4的相互作用。我们报告说,Pu27序列作为单体和更高阶的G-四链体物种的异质混合物存在于体外,并且该混合物可以通过尺寸排阻色谱法(SEC)分离而部分解决。在这种配置合奏中,可以通过修改缓冲液组成,退火程序和透析方案来更改平衡,从而影响所形成的G-四链体物种的分布。发现TMPyP4优先绑定到更高阶的G四联体物种,这表明通过卟啉末端堆积可以稳定c-Myc G四联体多聚体的连接。我们还检查了先前已报道的四个修饰的c-​​Myc序列,发现与亲本Pu27序列相比,四链体构型分布更窄。我们不能确切地得出结论,这些G四联体结构是从原始集合中选择还是它们是新的G四联体结构。由于这些序列与野生型启动子序列有很大不同,因此尚不清楚它们的结构是否具有任何实际的生物学相关性。还需要其他研究来研究G-四链体的多态性如何影响c-Myc和其他G-四链体的体外数据解释。此处报道的发现表明,实验条件对G-四链体的形成有重要作用,应仔细考虑,控制和详细报告。

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