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DWE: Discriminating word enumerator

机译:DWE:区分单词枚举器

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Motivation: Tissue-specific transcription factor binding sites give insight into tissue-specific transcription regulation.Results: We describe a word-counting-based tool for de novo tissue-specific transcription factor binding site discovery using expression information in addition to sequence information. We incorporate tissue-specific gene expression through gene classification to positive expression and repressed expression. We present a direct statistical approach to find overrepresented transcription factor binding sites in a foreground promoter sequence set against a background promoter sequence set. Our approach naturally extends to synergistic transcription factor binding site search.We find putative transcription factor binding sites that are overrepresented in the proximal promoters of liver-specific genes relative to proximal promoters of liver-independent genes. Our results indicate that binding sites for hepatocyte nuclear factors (especially HNF-1 and HNF-4) and CCAAT/enhancer-binding protein (C/EBPbeta) are the most overrepresented in proximal promoters of liver-specific genes. Our results suggest that HNF-4 has strong synergistic relationships with HNF-1, HNF-4 and HNF-3beta and with C/EBPbeta.
机译:动机:组织特异性转录因子结合位点深入了解组织特异性转录调控。结果:我们描述了基于单词计数的工具,除了序列信息外,还使用表达信息从头发现组织特异性转录因子结合位点。我们通过基因分类将组织特异性基因表达纳入阳性表达和抑制表达。我们提出了一种直接的统计方法,以找到针对背景启动子序列集的前景启动子序列集中过度表达的转录因子结合位点。我们的方法自然地扩展到协同转录因子结合位点搜索。我们发现推定的转录因子结合位点在肝脏特异性基因的近端启动子相对于肝脏独立基因的近端启动子中过分表达。我们的结果表明,肝细胞核因子(特别是HNF-1和HNF-4)和CCAAT /增强子结合蛋白(C / EBPbeta)的结合位点在肝特异性基因的近端启动子中最明显。我们的结果表明,HNF-4与HNF-1,HNF-4和HNF-3beta以及与C / EBPbeta具有很强的协同关系。

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