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全基因组近端启动子分析与解读

Genome-wide proximal promoter analysis and interpretation.

作者信息

Guruceaga Elizabeth, Segura Victor, Corrales Fernando J, Rubio Angel

机构信息

CEIT, Centro de Estudios e Investigaciones Técnicas de Gipuzkoa, San Sebastian, Spain.

出版信息

Methods Mol Biol. 2010;593:157-74. doi: 10.1007/978-1-60327-194-3_8.

Abstract

High-throughput gene expression technologies based on DNA microarrays allow the examination of biological systems. However, the interpretation of the complex molecular descriptions generated by these approaches is still challenging. The development of new methodologies to identify common regulatory mechanisms involved in the control of the expression of a set of co-expressed genes might enhance our capacity to extract functional information from genomic data sets. In this chapter, we describe a method that integrates different sources of information: gene expression data, genome sequence information, described transcription factor binding sites (TFBSs), functional information, and bibliographic data. The starting point of the analysis is the extraction of promoter sequences from a whole genome and the detection of TFBSs in each gene promoter. This information allows the identification of enriched TFBSs in the proximal promoter of differentially expressed genes. The functional and bibliographic interpretation of the results improves our biological insight into the regulatory mechanisms involved in a microarray experiment.

摘要

基于DNA微阵列的高通量基因表达技术能够对生物系统进行检测。然而,解读这些方法所产生的复杂分子描述仍然具有挑战性。开发新方法以识别参与一组共表达基因表达调控的共同调控机制,可能会增强我们从基因组数据集中提取功能信息的能力。在本章中,我们描述了一种整合不同信息源的方法:基因表达数据、基因组序列信息、已描述的转录因子结合位点(TFBS)、功能信息和文献数据。分析的起点是从全基因组中提取启动子序列,并检测每个基因启动子中的TFBS。这些信息有助于识别差异表达基因近端启动子中富集的TFBS。对结果进行功能和文献解读,可增进我们对微阵列实验中涉及的调控机制的生物学理解。

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