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大规模分析人类功能转录因子结合揭示了强烈偏向转录起始位点的现象。

Wide-scale analysis of human functional transcription factor binding reveals a strong bias towards the transcription start site.

机构信息

Department of Physics of Complex Systems, Weizmann Institute of Science, Rehovot, Israel.; Department of Molecular Cell Biology, Weizmann Institute of Science, Rehovot, Israel.

出版信息

PLoS One. 2007 Aug 29;2(8):e807. doi: 10.1371/journal.pone.0000807.

Abstract

BACKGROUND

Transcription factors (TF) regulate expression by binding to specific DNA sequences. A binding event is functional when it affects gene expression. Functionality of a binding site is reflected in conservation of the binding sequence during evolution and in over represented binding in gene groups with coherent biological functions. Functionality is governed by several parameters such as the TF-DNA binding strength, distance of the binding site from the transcription start site (TSS), DNA packing, and more. Understanding how these parameters control functionality of different TFs in different biological contexts is a must for identifying functional TF binding sites and for understanding regulation of transcription.

METHODOLOGY/PRINCIPAL FINDINGS: We introduce a novel method to screen the promoters of a set of genes with shared biological function (obtained from the functional Gene Ontology (GO) classification) against a precompiled library of motifs, and find those motifs which are statistically over-represented in the gene set. More than 8,000 human (and 23,000 mouse) genes, were assigned to one of 134 GO sets. Their promoters were searched (from 200 bp downstream to 1,000 bp upstream the TSS) for 414 known DNA motifs. We optimized the sequence similarity score threshold, independently for every location window, taking into account nucleotide heterogeneity along the promoters of the target genes. The method, combined with binding sequence and location conservation between human and mouse, identifies with high probability functional binding sites for groups of functionally-related genes. We found many location-sensitive functional binding events and showed that they clustered close to the TSS. Our method and findings were tested experimentally.

CONCLUSIONS/SIGNIFICANCE: We identified reliably functional TF binding sites. This is an essential step towards constructing regulatory networks. The promoter region proximal to the TSS is of central importance for regulation of transcription in human and mouse, just as it is in bacteria and yeast.

摘要

背景

转录因子 (TF) 通过与特定的 DNA 序列结合来调节基因表达。当结合事件影响基因表达时,它就是功能性的。结合序列在进化过程中的保守性以及在具有一致生物学功能的基因群中过度表达的情况反映了其功能。功能受几个参数的控制,如 TF-DNA 结合强度、结合位点与转录起始位点 (TSS) 的距离、DNA 包装等。了解这些参数如何在不同的生物背景下控制不同 TF 的功能,对于识别功能性 TF 结合位点和理解转录调控是必不可少的。

方法/主要发现:我们引入了一种新方法,用于筛选具有共同生物学功能(从功能基因本体论 (GO) 分类中获得)的一组基因的启动子,与预编译的基序文库进行对比,并找到在基因集中统计上过度表达的基序。超过 8000 个人类(和 23000 个小鼠)基因被分配到 134 个 GO 集合中的一个。从 TSS 下游 200 bp 到上游 1000 bp 搜索它们的启动子,寻找 414 个已知的 DNA 基序。我们针对每个位置窗口独立地优化了序列相似性得分阈值,同时考虑到目标基因启动子中核苷酸的异质性。该方法结合了人与小鼠之间的结合序列和位置保守性,可高度准确地识别功能相关基因的功能结合位点。我们发现了许多位置敏感的功能性结合事件,并表明它们聚集在 TSS 附近。我们的方法和发现已经过实验验证。

结论/意义:我们可靠地鉴定了功能性 TF 结合位点。这是构建调控网络的重要步骤。正如在细菌和酵母中一样,TSS 附近的启动子区域对于人类和小鼠的转录调控至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd61/1950076/d2f23c52e222/pone.0000807.g001.jpg

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