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Accessibility of microRNA binding sites in metastable RNA secondary structures in the presence of SNPs

机译:SNP存在下亚稳态RNA二级结构中microRNA结合位点的可及性

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Motivation: We study microRNA (miRNA) bindings to metastable RNA secondary structures close to minimum free energy conformations in the context of single nucleotide polymorphisms (SNPs) and messenger RNA (mRNA) concentration levels, i.e. whether features of miRNA bindings to metastable conformations could provide additional information supporting the differences in expression levels of the two sequences defined by a SNP. In our study, the instances [mRNA/3 ' UTR; SNP; miRNA] were selected based on strong expression level analyses, SNP locations within binding regions and the computationally feasible identification of metastable conformations. Results: We identified 14 basic cases [mRNA; SNP; miRNA] of 30 UTR-lengths ranging from 124 up to 1078 nt reported in recent literature, and we analyzed the number, structure and miRNA binding to metastable conformations within an energy offset delta E above mfe conformations. For each of the 14 instances, the miRNA binding characteristics are determined by the corresponding STarMir output. Among the different parameters we introduced and analyzed, we found that three of them, related to the average depth and average opening energy of metastable conformations, may provide supporting information for a stronger separation between miRNA bindings to the two alleles defined by a given SNP.
机译:动机:我们研究了在单核苷酸多态性(SNP)和信使RNA(mRNA)浓度水平的情况下,微小RNA(miRNA)与亚稳RNA二级结构的结合接近最小自由能构象,即miRNA与亚稳构象结合的特征是否可以提供支持由SNP定义的两个序列表达水平差异的其他信息。在我们的研究中,[mRNA / 3'UTR; SNP;基于强表达水平分析,结合区域内SNP位置以及亚稳构象的计算可行性鉴定,选择了[miRNA]。结果:我们确定了14个基本病例[mRNA; SNP; [miRNA]在最近文献中报道了30种UTR长度,范围从124到1078 nt,我们分析了在mfe构型以上的能量偏移δE内与亚稳构型结合的数量,结构和miRNA。对于这14个实例中的每个实例,miRNA结合特性由相应的STarMir输出确定。在我们引入和分析的不同参数中,我们发现其中三个与亚稳构象的平均深度和平均打开能量有关,可能为miRNA与给定SNP定义的两个等位基因结合之间的更强分离提供支持信息。

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