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DoOPSearch: a web-based tool for finding and analysing common conserved motifs in the promoter regions of different chordate and plant genes

机译:DoOPSearch:一种基于网络的工具,用于查找和分析不同碳酸盐和植物基因的启动子区域中常见的保守基序

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Background The comparative genomic analysis of a large number of orthologous promoter regions of the chordate and plant genes from the DoOP databases shows thousands of conserved motifs. Most of these motifs differ from any known transcription factor binding site (TFBS). To identify common conserved motifs, we need a specific tool to be able to search amongst them. Since conserved motifs from the DoOP databases are linked to genes, the result of such a search can give a list of genes that are potentially regulated by the same transcription factor(s). Results We have developed a new tool called DoOPSearch http://doopsearch.abc.hu for the analysis of the conserved motifs in the promoter regions of chordate or plant genes. We used the orthologous promoters of the DoOP database to extract thousands of conserved motifs from different taxonomic groups. The advantage of this approach is that different sets of conserved motifs might be found depending on how broad the taxonomic coverage of the underlying orthologous promoter sequence collection is (consider e.g. primates vs. mammals or Brassicaceae vs. Viridiplantae ). The DoOPSearch tool allows the users to search these motif collections or the promoter regions of DoOP with user supplied query sequences or any of the conserved motifs from the DoOP database. To find overrepresented gene ontologies, the gene lists obtained can be analysed further using a modified version of the GeneMerge program. Conclusion We present here a comparative genomics based promoter analysis tool. Our system is based on a unique collection of conserved promoter motifs characteristic of different taxonomic groups. We offer both a command line and a web-based tool for searching in these motif collections using user specified queries. These can be either short promoter sequences or consensus sequences of known transcription factor binding sites. The GeneMerge analysis of the search results allows the user to identify statistically overrepresented Gene Ontology terms that might provide a clue on the function of the motifs and genes.
机译:背景从DoOP数据库对大量的碳酸盐和植物基因的直系同源启动子区域进行的比较基因组分析表明,有数千个保守的基序。这些基序大多数与任何已知的转录因子结合位点(TFBS)不同。为了识别常见的保守主题,我们需要一种特定的工具来搜索它们。由于来自DoOP数据库的保守基序与基因相关联,因此这种搜索的结果可以给出可能受相同转录因子调控的基因列表。结果我们开发了一种名为DoOPSearch的新工具http://doopsearch.abc.hu,用于分析含碳酸盐或植物基因启动子区域中的保守基序。我们使用DoOP数据库的直系同源启动子从不同分类组中提取了数千个保守基序。该方法的优点是,取决于基础直向启动子序列集合的分类学覆盖范围有多广(可以考虑例如灵长类动物对哺乳动物或十字花科对病毒科),可以找到不同的保守基元集。 DoOPSearch工具允许用户使用用户提供的查询序列或DoOP数据库中的任何保守基元来搜索这些基序集合或DoOP的启动子区域。为了找到过度代表的基因本体,可以使用修改后的GeneMerge程序进一步分析获得的基因列表。结论我们在这里介绍了一种基于比较基因组的启动子分析工具。我们的系统基于不同分类组特征的保守启动子基元的独特集合。我们提供命令行和基于Web的工具,用于使用用户指定的查询来搜索这些图案集合。这些可以是短启动子序列或已知转录因子结合位点的共有序列。搜索结果的GeneMerge分析使用户能够识别出统计学上过分代表的基因本体论术语,这些术语可能会提供有关基序和基因功能的线索。

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