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COPS: Detecting Co-Occurrence and Spatial Arrangement of Transcription Factor Binding Motifs in Genome-Wide Datasets

机译:COPS:检测全基因组数据集中转录因子结合基序的同时发生和空间排列

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摘要

In multi-cellular organisms, spatiotemporal activity of cis-regulatory DNA elements depends on their occupancy by different transcription factors (TFs). In recent years, genome-wide ChIP-on-Chip, ChIP-Seq and DamID assays have been extensively used to unravel the combinatorial interaction of TFs with cis-regulatory modules (CRMs) in the genome. Even though genome-wide binding profiles are increasingly becoming available for different TFs, single TF binding profiles are in most cases not sufficient for dissecting complex regulatory networks. Thus, potent computational tools detecting statistically significant and biologically relevant TF-motif co-occurrences in genome-wide datasets are essential for analyzing context-dependent transcriptional regulation. We have developed COPS (Co-Occurrence Pattern Search), a new bioinformatics tool based on a combination of association rules and Markov chain models, which detects co-occurring TF binding sites (BSs) on genomic regions of interest. COPS scans DNA sequences for frequent motif patterns using a Frequent-Pattern tree based data mining approach, which allows efficient performance of the software with respect to both data structure and implementation speed, in particular when mining large datasets. Since transcriptional gene regulation very often relies on the formation of regulatory protein complexes mediated by closely adjoining TF binding sites on CRMs, COPS additionally detects preferred short distance between co-occurring TF motifs. The performance of our software with respect to biological significance was evaluated using three published datasets containing genomic regions that are independently bound by several TFs involved in a defined biological process. In sum, COPS is a fast, efficient and user-friendly tool mining statistically and biologically significant TFBS co-occurrences and therefore allows the identification of TFs that combinatorially regulate gene expression.
机译:在多细胞生物中,顺式调控DNA元件的时空活性取决于它们被不同转录因子(TF)占据的时间。近年来,全基因组芯片上芯片,ChIP-Seq和DamID检测已被广泛用于揭示基因组中TF与顺式调控模块(CRM)的组合相互作用。即使越来越多的全基因组结合图谱可用于不同的TF,但在大多数情况下,单个TF结合谱图不足以剖析复杂的调控网络。因此,检测全基因组数据集中具有统计学意义和生物学相关的TF-基序共存的有效计算工具对于分析上下文相关的转录调控至关重要。我们已经开发了COPS(共现模式搜索),这是一种新的生物信息学工具,基于关联规则和马尔可夫链模型的组合,可检测感兴趣的基因组区域中共现的TF结合位点(BS)。 COPS使用基于频繁模式树的数据挖掘方法扫描DNA序列中的频繁基序模式,这使得软件在数据结构和实现速度方面都具有高效的性能,尤其是在挖掘大型数据集时。由于转录基因调控通常依赖于CRM上紧密相邻的TF结合位点介导的调控蛋白复合物的形成,因此COPS还可以检测到同时出现的TF基序之间的较短距离。使用三个已发布的数据集评估了我们软件在生物学意义上的性能,这些数据集包含基因组区域,这些基因组区域被定义的生物过程中涉及的多个TF独立地结合。总而言之,COPS是一种快速,高效且用户友好的工具,可从统计和生物学意义上挖掘重要的TFBS并发现象,因此可识别组合调控基因表达的TF。

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