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首页> 外文期刊>Angewandte Chemie >Adenine-Driven Structural Switch from a Two- to Three-Quartet DNA G-Quadruplex
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Adenine-Driven Structural Switch from a Two- to Three-Quartet DNA G-Quadruplex

机译:从两个到三重DNA G-QuadRuplex的腺嘌呤驱动的结构开关

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摘要

A G-rich sequence found in the regulatory region of the RANKL gene, which is associated with homeostasis of bone metabolism, folds into a two-quartet basket-type G-quadruplex stabilized by A center dot G center dot A and G center dot G center dot G base-triads. Perusal of local structural features together with G/A-to-T modifications uncovered the critical role of A5 for the formation of a distinct antiparallel two-quartet topology and not the three-quartet topology that would be expected based on the sequence with four GGG-tracts alone. The structural changes induced by the A5-to-T5 modification include a switch in orientation and relative positions of G-strands that together with anti to syn reorientation of G12 provide insights into the complexity of the interactions that influence the folding of G-rich DNA. Understanding the impact of loop residues on the stability and formation of G-quadruplexes advances our knowledge and ability to predict structures adopted by G-rich sequences, which are involved in regulatory mechanisms in the cell, and may also facilitate drug design.
机译:在RANKL基因的调节区中发现的富含G的序列,其与骨代谢的稳态相关,折叠成由中心点G中心点A和G中心点G稳定的双肉篮式G-Quadruplex中心点G基础三合会。局部结构特征与G / A-TO-T修改一起发现A5的关键作用,以形成不同的反平行双排拓扑,而不是基于四个GGG的序列所期望的三码拓扑却单独。 A5-To-T5修饰引起的结构变化包括与G12的抗体的G12一起的抗链和G12的相对位置的开关提供了影响影响富含G的抗体的相互作用的复杂性的见解。了解环路残留对G-Quadruplees的稳定性和形成的影响,我们的知识和能力预测了富含G的序列所采用的结构,这些序列参与细胞中的调节机制,也可以促进药物设计。

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