DNA-Like Duplex Structures Derived from Chemistry Based on 2’-Deoxy-Cytidine: A New Model for Base-Specific Inhibition of G and C on DNA and RNA Level

H. Buck
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引用次数: 0

Abstract

The new epigenetic elements 5-hydroxymethyl-dC, 5-formyl-dC, and 5-car- boxy-dC may be considered as intermediates of an active demethylation process. A comprehensive mechanistic model is given for the C-C bond cleavage focused on the chemistry within the DNA duplex structure. In addition we register spin-off chemistry of this process in evaluating new duplex systems closely related to natural DNA and RNA concerning their hydrogen-bond symmetrization. A model is composed for a base-specific inhibition of G and C on the DNA and RNA level. C-G combinations are of general importance in controlling the dynamics of gene expression. In some way the suggested model systems are related to antisense oligonucleotides (ASOs).
基于2'-脱氧胞苷的化学衍生DNA样双链结构:G和C在DNA和RNA水平上的碱基特异性抑制新模型
新的表观遗传元件5-羟甲基- dc、5-甲酰基- dc和5-car- box - dc可能被认为是活性去甲基化过程的中间产物。本文从DNA双工结构的化学性质出发,给出了C-C键断裂的综合机理模型。此外,我们还在评价与天然DNA和RNA密切相关的新双相体系的氢键对称性方面记录了该过程的衍生化学。建立了G和C在DNA和RNA水平上的碱基特异性抑制模型。C-G组合在控制基因表达动力学方面具有普遍的重要性。在某种程度上,所建议的模型系统与反义寡核苷酸(ASOs)有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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