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A Mechanistic Study of lncRNA Fendrr Regulation of FoxF1 Lung Cancer Tumor Supressor

机译:Foxnc肺癌抑制基因lncRNA Fendrr调控机制的研究

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Long non-coding RNAs are known to play multiple roles in the complex machinery of the cell. However, their recent addition to genomic research has increased the complexity of gene expression analyses. In this work, we perform a computational study that aims to contribute to the current understanding of the mechanisms that underlie the experimentally suggested interaction between the lncRNA Fendrr and FoxF1 lung cancer tumor suppressor in carcinogenesis. Results suggest that there exists indeed a multi-level interaction between Fendrr and FoxF1 promoter region, both direct via RNA-DNA:DNA triplex domain formation or mediated by proteins that interact simultaneously with the promoter region of FoxF1 and Fendrr transcripts. Moreover, the applied computational methodology can serve as a pipeline to process any candidate lncRNA-gene pair of interest and obtain putative sources of lncRNA-gene interaction.
机译:已知长的非编码RNA在细胞的复杂机制中起多种作用。但是,它们最近在基因组研究中的应用增加了基因表达分析的复杂性。在这项工作中,我们进行了一项计算研究,旨在为目前对lncRNA Fendrr和FoxF1肺癌肿瘤抑制因子在癌变过程中实验性相互作用的基础机制的理解做出贡献。结果表明,Fendrr和FoxF1启动子区域之间确实存在多级相互作用,既可以通过RNA-DNA:DNA三链体结构域直接形成,也可以通过与FoxF1和Fendrr转录子的启动子区域同时相互作用的蛋白质介导。而且,所应用的计算方法可以用作处理任何候选的感兴趣的lncRNA-基因对并获得lncRNA-基因相互作用的推定来源的管道。

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