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CONREAL: Conserved Regulatory Elements Anchored Alignment Algorithm for Identification of Transcription Factor Binding Sites by Phylogenetic Footprinting

机译:建议:保守的调节元件锚定比对算法,用于通过系统发生足迹识别转录因子结合位点

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摘要

Prediction of transcription-factor target sites in promoters remains difficult due to the short length and degeneracy of the target sequences. Although the use of orthologous sequences and phylogenetic footprinting approaches may help in the recognition of conserved and potentially functional sequences, correct alignment of the short transcription-factor binding sites can be problematic for established algorithms, especially when aligning more divergent species. Here, we report a novel phylogenetic footprinting approach, CONREAL, that uses biologically relevant information, that is, potential transcription-factor binding sites as represented by positional weight matrices, to establish anchors between orthologous sequences and to guide promoter sequence alignment. Comparison of the performance of CONREAL with the global alignment programs LAGAN and AVID using a reference data set, shows that CONREAL performs equally well for closely related species like rodents and human, and has a clear added value for aligning promoter elements of more divergent species like human and fish, as it identifies conserved transcription-factor binding sites that are not found by other methods. CONREAL is accessible via a Web interface at http://conreal.niob.knaw.nl/.
机译:由于靶序列的长度短且简并,因此难以预测启动子中的转录因子靶位点。尽管直系同源序列和系统进化足迹方法的使用可能有助于识别保守的和潜在的功能序列,但短转录因子结合位点的正确比对已建立的算法可能会出现问题,尤其是在比对更具差异性的物种时。在这里,我们报告了一种新颖的系统进化足迹方法,CONREAL,使用生物学相关信息,即潜在的转录因子结合位点(由位置权重矩阵表示),在直系同源序列之间建立锚点并指导启动子序列比对。使用参考数据将CONREAL与全球比对程序LAGAN和AVID的性能进行比较,表明CONREAL在密切相关的物种(如啮齿动物和人类)上的表现同样出色,并且在比对更多差异物种的启动子元件方面具有明显的附加值人类和鱼类,因为它可以识别其他方法找不到的保守转录因子结合位点。可通过Web界面http://conreal.niob.knaw.nl/访问CONREAL。

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