Identification of Over-Represented Combinations of Transcription Factor Binding Sites in Sets of Co-Expressed Genes

S. Huang, Debra L. Fulton, David J. Arenillas, P. Perco, S. Sui, J. Mortimer, W. Wasserman
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引用次数: 11

Abstract

Transcription regulation is mediated by combinatorial interactions between diverse trans-acting proteins and arrays of cis-regulatory sequences. Revealing this complex interplay between transcription factors and binding sites remains a fundamental problem for understanding the flow of genetic information. The oPOSSUM analysis system facilitates the interpretation of gene expression data through the analysis of transcription factor binding sites shared by sets of co-expressed genes. The system is based on cross-species sequence comparisons for phylogenetic footprinting and motif models for binding site prediction. We introduce a new set of analysis algorithms for the study of the combinatorial properties of transcription factor binding sites shared by sets of co-expressed genes. The new methods circumvent computational challenges through an applied focus on families of transcription factors with similar binding properties. The algorithm accurately identifies combinations of binding sites over-represented in reference collections and clarifies the results obtained by existing methods for the study of isolated binding sites.
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鉴定共表达基因组中转录因子结合位点的过度代表组合
转录调节是由多种反式作用蛋白和顺式调节序列阵列之间的组合相互作用介导的。揭示转录因子和结合位点之间复杂的相互作用仍然是理解遗传信息流的一个基本问题。oPOSSUM分析系统通过分析共表达基因组共享的转录因子结合位点,促进了基因表达数据的解释。该系统是基于跨物种序列比较的系统发育足迹和基序模型的结合位点预测。我们引入了一套新的分析算法来研究转录因子结合位点的组合特性,这些位点是由共表达基因共享的。新方法通过应用于具有相似结合特性的转录因子家族来规避计算挑战。该算法准确地识别了在参考文献集中被过度代表的结合位点组合,并澄清了现有方法获得的孤立结合位点研究结果。
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