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Please use this identifier to cite or link to this item: http://ntour.ntou.edu.tw:8080/ir/handle/987654321/27114

Title: Identification of Potential E2F Target Genes Through cis-regulatory Modules Derived From Chromatin Immunoprecipitation Microarray Data
Authors: Wen-Shyong Tzou
Contributors: NTOU:Institute of Bioscience and Biotechnology
國立臺灣海洋大學:生物科技研究所
Keywords: ChIP-chip;cis-regulatory module;E2F;transcription factor binding sites
Date: 2010-05
Issue Date: 2011-10-21T02:22:48Z
Publisher: Fooyin Journal of Health Sciences
Abstract: Abstract:In the postgenome era, employment of high-throughput data via the integrated use of resources from various domains will lead to the generation of new knowledge and testable hypothesis. In this bioinformatic research, we utilized published chromatin immunoprecipitation microarray (ChIP-chip) results for the promoter binding by E2F1 or E2F4 proteins observed in the primary human WI-38 cells to infer the potential transcription factor binding sites (TFBS). We have compiled “gene vs. motif” and “motif vs. gene” tables from more than 2,700,000 computational predicted transcriptional regulatory motifs representing the regulatory potential for 230 transcription factors families within the proximal promoter sequence (1,200 nucleotides) of human genome. From this approach, for the first time, the transcription of 23 genes is predicted to be under the control of a cis-regulatory module containing four TFBS motifs (CREB, E2F, NF-Y and Nrf-1).
Relation: 2(2), pp.66–70
URI: http://ntour.ntou.edu.tw/handle/987654321/27114
Appears in Collections:[生命科學暨生物科技學系] 期刊論文

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