首页> 外文会议>Pacific symposium on biocomputing >WHOLE GENOME HUMAN/MOUSE PHYLOGENETIC FOOTPRINTING OF POTENTIAL TRANSCRIPTION REGULATORY SIGNALS
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WHOLE GENOME HUMAN/MOUSE PHYLOGENETIC FOOTPRINTING OF POTENTIAL TRANSCRIPTION REGULATORY SIGNALS

机译:全基因组人/小鼠系统源转录调控信号的脚印

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Phylogenetic footprinting is an efficient approach for revealing potential transcription factor binding sites in promoter sequences. The idea is based on an assumption that functional sites in promoters should evolve much slower then other regions that do not bear any conservative function. Therefore, potential transcription factor (TF) binding sites that are found in the evolutionally conservative regions of promoters have more chances to be considered as "real" sites. The most difficult step of the phylogenetic footprinting is alignment of promoter sequences between different organisms (f.e. human and mouse). The conventional alignment methods often can not align promoters due to the high level of sequence variability. We have developed a new alignment method that takes into account similarity in distribution of potential binding sites (motif-based alignment). This method has been used effectively for promoter alignment and for revealing new potential binding sites for various transcription factors. We made a systematic phylogenetic footprinting of human/mouse conserved non-coding sequences (CNS). 60 thousand potential binding sites were revealed in human and mouse genomes. We have developed a database of the predicted potential TF binding sites.
机译:系统发育足迹是一种有效的方法,用于揭示促进剂序列中的潜在转录因子结合位点。该想法是基于假设,该启动子的功能位点应该演变得多,然后不承受任何保守功能的区域。因此,在启动子的进化保守区域中发现的潜在转录因子(TF)结合位点具有更多的机会被视为“真实”的位点。系统发育足迹的最困难的步骤是不同生物(F.e.人和小鼠)之间的启动子序列的对准。传统的对准方法通常不能对序列变异性级别的高水平变化来对准启动子。我们开发了一种新的对准方法,该方法考虑了潜在绑定站点的分布(基于主题的对齐)的相似性。该方法已经有效地用于启动子对准,并用于揭示各种转录因子的新潜在结合位点。我们制造了人/小鼠保守的非编码序列(CNS)的系统系统发育脚印。在人和小鼠基因组中揭示了60万潜在的结合位点。我们已经开发了预测潜在的TF绑定站点的数据库。

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