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Understanding the Effect of Locked Nucleic Acid and 2′-O-Methyl Modification on the Hybridization Thermodynamics of a miRNA?mRNA Pair in the Presence and Absence of AfPiwi Protein

机译:理解锁定核酸和2'-O-甲基修饰对MiRNA杂交热力学的影响,在AFPIWI蛋白的存在和不存在下MRNA对

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摘要

miRNAs are some of the key epigenetic regulators of gene expression. They act through hybridization with their target mRNA and modulate the level of respective proteins via different mechanisms. Various cancer conditions are known to be associated with up- and downregulation of the oncogenic and tumor suppressor miRNAs, respectively. The levels of aberrantly expressed oncogenic miRNAs can be downregulated in different ways. Similarly, restoration of tumor suppressor miRNAs to their normal levels can be achieved using miRNA mimics. However, the use of miRNA mimics is limited by their reduced biostability and function. We have studied the hybridization thermodynamics of the miRNA 26a (11-mer, including the seed sequence) guide strand with the mRNA (11-mer) target strand in the absence and presence of AfPiwi protein. We have also inserted locked nucleic acids (LNAs) and 2′-O-methyl-modified nucleotides into the guide strand, in a walk-through manner, to assess their effect on the binding efficiency between guide and target RNA. Insertion of LNA and 2′-O-methyl-modified nucleotides into the guide strand helped to strengthen the binding affinity irrespective of the position of insertion. However, in the presence of AfPiwi protein, these modifications reduced the binding affinity to different extents depending on the position of insertion. Insertion of a modification leads to an increase in the enthalpic contribution with an increased unfavorable entropic contribution, which negatively compensates for the higher favorable enthalpy.
机译:miRNA是基因表达的一些关键的表观遗传调节因子。它们通过与其靶mRNA的杂交起作用,并通过不同的机制调节各种蛋白质的水平。已知各种癌症条件分别与癌肠和肿瘤抑制米兰的上调和下调相关。异常表达的致力生成miRNA的水平可以以不同的方式下调。类似地,可以使用miRNA模拟可以实现肿瘤抑制miRNA对其正常水平的恢复。然而,使用miRNA模仿的使用受到减少的生物稳定性和功能。我们已经研究了miRNA 26a(11-mer,包括种子序列)引导股线的杂交热力学,在不存在和存在Afpiwi蛋白的情况下具有mRNA(11-ME1)靶链。我们还将锁定的核酸(LNA)和2'-O-甲基修饰的核苷酸以步进方式插入引导股,以评估它们对引导和靶RNA之间的结合效率的影响。将LNA和2'-O-甲基改性的核苷酸插入引导股线中有助于加强结合亲和力,无论插入的位置如何。然而,在AFPIWI蛋白质存在下,这些修饰根据插入的位置而降低了不同范围的结合亲和力。插入修改导致焓贡献的增加随着不利的熵贡献而导致促进的贡献增加,这对较高的有利焓造成负赔偿。

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