Prediction and experimental validation of novel STAT3 target genes in human cancer cells

PLoS One. 2009 Sep 4;4(9):e6911. doi: 10.1371/journal.pone.0006911.

Abstract

The comprehensive identification of functional transcription factor binding sites (TFBSs) is an important step in understanding complex transcriptional regulatory networks. This study presents a motif-based comparative approach, STAT-Finder, for identifying functional DNA binding sites of STAT3 transcription factor. STAT-Finder combines STAT-Scanner, which was designed to predict functional STAT TFBSs with improved sensitivity, and a motif-based alignment to minimize false positive prediction rates. Using two reference sets containing promoter sequences of known STAT3 target genes, STAT-Finder identified functional STAT3 TFBSs with enhanced prediction efficiency and sensitivity relative to other conventional TFBS prediction tools. In addition, STAT-Finder identified novel STAT3 target genes among a group of genes that are over-expressed in human cancer cells. The binding of STAT3 to the predicted TFBSs was also experimentally confirmed through chromatin immunoprecipitation. Our proposed method provides a systematic approach to the prediction of functional TFBSs that can be applied to other TFs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Algorithms
  • Animals
  • Binding Sites
  • Cell Line, Tumor
  • Cluster Analysis
  • Computational Biology / methods
  • Gene Expression Regulation, Neoplastic*
  • Genome
  • Humans
  • Mice
  • Models, Biological
  • Oligonucleotide Array Sequence Analysis
  • Promoter Regions, Genetic
  • STAT3 Transcription Factor / metabolism*
  • Transcription Factors / metabolism

Substances

  • STAT3 Transcription Factor
  • STAT3 protein, human
  • Transcription Factors