A high resolution genome-wide scan of HNF4α recognition sites infers a regulatory gene network in colon cancer

• Published in: PloS one Vol. 6; no. 7; p. e21667
• Main Authors: Weltmeier, Fridtjof, Borlak, Juergen
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 2011; Public Library of Science (PLoS)
• Subjects: Activator protein 1; Algorithms; Apolipoproteins; Binding Sites; Biology; Biomarkers, Tumor - genetics; Cancer; Chromatin; Chromatin Immunoprecipitation; Chromosomes; Colon; Colon cancer; Colonic Neoplasms - genetics; Colonic Neoplasms - metabolism; Colorectal cancer; Deoxyribonucleic acid; Diabetes; Disease control; DNA; DNA, Neoplasm - genetics; DNA-Binding Proteins - genetics; DNA-Binding Proteins - metabolism; Enhancer Elements, Genetic; Estrogens; Experiments; Gene expression; Gene Expression Profiling; Gene Expression Regulation; Gene Regulatory Networks; Genes; Genetic algorithms; Genome, Human; Genomes; Genomics; Hepatitis; Hepatocyte Nuclear Factor 4 - genetics; Hepatocyte Nuclear Factor 4 - metabolism; Humans; Medicine; Metabolism; Oligonucleotide Array Sequence Analysis; Pilot projects; Promoter Regions, Genetic - genetics; Protein Binding; Proteins; Real-Time Polymerase Chain Reaction; Ribonucleic acid; RNA; RNA processing; Rodents; Toxicology; Transcription factors; Transcription Factors - genetics; Transcription Factors - metabolism; Tumor Cells, Cultured; Y chromosomes; Germany
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0021667

The hepatic nuclear factor HNF4α is a versatile transcription factor and controls expression of many genes in development, metabolism and disease. To delineate its regulatory gene network in colon cancer and to define novel gene targets a comprehensive genome-wide scan was carried out at a resolution of 35 bp with chromatin IP DNA obtained from the human colon carcinoma cell line Caco-2 that is a particularly rich source of HNF4α. More than 90% of HNF4α binding sites were mapped as promoter distal sequences while enhancer elements could be defined to foster chromatin loops for interaction with other promoter-bound transcription factors. Sequence motif analysis by various genetic algorithms evidenced a unique enhanceosome that consisted of the nuclear proteins ERα, AP1, GATA and HNF1α as cooperating transcription factors. Overall >17,500 DNA binding sites were identified with a gene/binding site ratio that differed >6-fold between chromosomes and clustered in distinct chromosomal regions amongst >6600 genes targeted by HNF4α. Evidence is presented for nuclear receptor cross-talk of HNF4α and estrogen receptor α that is recapitulated at the sequence level. Remarkably, the Y-chromosome is devoid of HNF4α binding sites. The functional importance of enrichment sites was confirmed in genome-wide gene expression studies at varying HNF4α protein levels. Taken collectively, a genome-wide scan of HNF4α binding sites is reported to better understand basic mechanisms of transcriptional control of HNF4α targeted genes. Novel promoter distal binding sites are identified which form an enhanceosome thereby facilitating RNA processing events.