MCF7细胞系TCF7L2结合位点分级调控网络的推断

Q4 Pharmacology, Toxicology and Pharmaceutics International Journal of Computational Biology and Drug Design Pub Date : 2016-02-29 DOI:10.1504/IJCBDD.2016.074990
Yao Wang, Rui Wang, V. Jin
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引用次数: 2

摘要

TCF7L2转录因子(TF)是Wnt信号通路的一员,可能通过结合不同的调控区域影响多种基因的转录。全基因组研究已经确定了数千个TCF7L2结合位点,并揭示了一些相关的TF伴侣。然而,在MCF7细胞中TCF7L2及其伴生tf的分层调控网络中,仍有很大的未知区域。我们通过基于tf特定位置权重矩阵(PWM)在富集峰区域搜索基序来分析ChIP-seq数据。我们发现FOXO1和CAD与上调基因有关,AP2α、PBF和AP1与下调基因有关。TCF7L2和GATA3均与上调和下调基因相关。本研究通过挖掘MCF7细胞的ChIP-seq数据,发现了新的TCF7L2相关调控网络,这可能有助于进一步研究Wnt通路在乳腺癌或其他疾病中的相关机制。
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Inference of hierarchical regulatory network of TCF7L2 binding sites in MCF7 cell line
The TCF7L2 transcription factor (TF) is a member of Wnt signalling pathway, and may influence transcription of several genes by binding to distinct regulatory regions. Genome-wide studies have identified thousands of TCF7L2 binding sites and have revealed some associated TF partners. However, there is still a large uncharted region in the hierarchical regulatory network for TCF7L2 and the partner TFs in MCF7 cells. We analysed ChIP-seq data by searching for motifs in the enriched peak region based on TF-specific position weight matrix (PWM). We found association of FOXO1 and CAD with up-regulated genes, AP2α, PBF and AP1 with down-regulated genes. TCF7L2 and GATA3 were found to be associated with both up and down-regulated genes. Our study uncovers new TCF7L2 associated regulatory networks by mining ChIP-seq data in MCF7 cell, which may contribute to further study of the mechanisms related to Wnt pathway in breast cancer or other diseases.
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来源期刊
International Journal of Computational Biology and Drug Design
International Journal of Computational Biology and Drug Design Pharmacology, Toxicology and Pharmaceutics-Drug Discovery
CiteScore
1.00
自引率
0.00%
发文量
8
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