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基于新距离测度的 TF 映射进行启动子序列比较的计算方法。

Computational approach towards promoter sequence comparison via TF mapping using a new distance measure.

机构信息

B.M.S College of Engineering, Bull Temple Road, Bangalore, 560019, India.

出版信息

Interdiscip Sci. 2011 Mar;3(1):43-9. doi: 10.1007/s12539-011-0057-x. Epub 2011 Mar 3.

Abstract

We propose a method for identifying transcription factor binding sites (TFBS) in the given promoter sequence and mapping the transcription factors (TFs). The proposed algorithm searches the +1 transcription start site (TSS) for eukaryotic and prokaryotic sequences individually. The algorithm was tested with sequences from both eukaryotes and prokaryotes for at least 9 experimentally verified and validated functional TFs in promoter sequences. The order and type of TF binding to the promoter of genes encoding central metabolic pathway (CMP) enzyme was tabulated. A new similarity measure was devised for scoring the similarity between a pair of promoter sequences based on the number and order of motifs. Further, these were grouped in clusters considering the scores between them. The distance between each of the clusters in individual pathway was calculated and a phylogenetic tree was developed. This method is further applied to other pathways such as lipid and amino acid biosynthesis to retrieve and compare experimentally verified and conserved TFBS.

摘要

我们提出了一种方法,用于识别给定启动子序列中的转录因子结合位点 (TFBS) 并对转录因子 (TF) 进行映射。该算法分别针对真核生物和原核生物序列在 +1 转录起始位点 (TSS) 进行搜索。该算法使用来自真核生物和原核生物的序列对至少 9 个在启动子序列中经过实验验证和验证的功能 TF 进行了测试。对基因编码中心代谢途径 (CMP) 酶的启动子中 TF 结合的顺序和类型进行了制表。设计了一种新的相似性度量标准,用于根据基序的数量和顺序对一对启动子序列之间的相似性进行评分。此外,还根据它们之间的得分将它们分组到聚类中。计算了各个途径中每个聚类之间的距离,并开发了一个系统发育树。该方法进一步应用于脂质和氨基酸生物合成等其他途径,以检索和比较经过实验验证和保守的 TFBS。

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Positional distribution of human transcription factor binding sites.人类转录因子结合位点的位置分布。
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