一个新的管道motif发现,修剪和验证启动子序列的人类组织特异性基因

X. Gong, Hua Yu, F. Zhao
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引用次数: 0

摘要

组织特异性(TS)基因的鉴定和分析及其调控活性在了解生物体机制、疾病诊断和药物设计方面发挥着重要作用。在本文中,我们设计了一个管道来发现组织特异性基因的启动子基序。该流程包括三个阶段:基序搜索、基序合并和基序验证。motif搜索阶段集成了三种算法:MEME、AlignACE和Gibbs Sampling。在第二阶段,我们提出了一种基于贝叶斯概率原理的基序合并方法,以减少第一阶段的基序冗余。最后,基序验证阶段使用贝叶斯假设检验方法验证发现的基序的统计显著性。我们对82个组织中4,552个人类组织特异性基因和924个管家基因的启动子区(-449bp-1000bp)序列进行了分析。基序在不同启动子区域的分布表明,大多数基序倾向于在启动子的近端区域(+500~50bp, -50bp~-500bp)。
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A novel pipeline for motif discovery, pruning and validation in promoter sequences of human tissue specific genes
Identification and analysis of tissue-specific (TS) genes and their regulatory activities play an important role in the understanding of mechanisms of organisms, disease diagnosis and drug design. In this paper, we designed a pipeline for the discovery of promoter motifs for tissue-specific genes. The pipeline consists of three phases: motif searching, motif merging and motif validation. The motif searching phase integrated three algorithms: MEME, AlignACE and Gibbs Sampling. In the second phase, we proposed a motif merging method, which is based on Bayesian probabilistic principles, to reduce redundancies of motifs from the first phase. Lastly, the motif validation phase verified the statistical significance of discovered motifs using a Bayesian Hypothesis Test approach. We performed the analysis on the sequences of promoter regions (-449bp-1000bp) of 4,552 human tissue-specific genes across 82 tissues and 924 housekeeping genes. The distributions of motifs in different promoter regions show that most motifs prefer to be in the proximal region (+500~50bp, -50bp~-500bp) of promoters.
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