51. Genome-wide prediction of mammalian enhancers based on analysis of transcription-factor binding affinity.
- Author
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Hallikas O, Palin K, Sinjushina N, Rautiainen R, Partanen J, Ukkonen E, and Taipale J
- Subjects
- Amino Acid Sequence, Animals, Carrier Proteins genetics, Carrier Proteins metabolism, Chickens, Computational Biology methods, Drosophila, Drosophila Proteins genetics, Drosophila Proteins metabolism, Gene Expression Regulation physiology, Genes, myc physiology, Hedgehog Proteins, Humans, Membrane Glycoproteins genetics, Membrane Glycoproteins metabolism, Mice, Molecular Sequence Data, Protein Binding physiology, Rats, Signal Transduction genetics, Signal Transduction physiology, Tetraodontiformes, Tumor Suppressor Protein p53 genetics, Wnt Proteins genetics, Wnt Proteins metabolism, Enhancer Elements, Genetic genetics, Genome, Oligonucleotide Array Sequence Analysis methods, Transcription Factors metabolism
- Abstract
Understanding the regulation of human gene expression requires knowledge of the "second genetic code," which consists of the binding specificities of transcription factors (TFs) and the combinatorial code by which TF binding sites are assembled to form tissue-specific enhancer elements. Using a novel high-throughput method, we determined the DNA binding specificities of GLIs 1-3, Tcf4, and c-Ets1, which mediate transcriptional responses to the Hedgehog (Hh), Wnt, and Ras/MAPK signaling pathways. To identify mammalian enhancer elements regulated by these pathways on a genomic scale, we developed a computational tool, enhancer element locator (EEL). We show that EEL can be used to identify Hh and Wnt target genes and to predict activated TFs based on changes in gene expression. Predictions validated in transgenic mouse embryos revealed the presence of multiple tissue-specific enhancers in mouse c-Myc and N-Myc genes, which has implications for organ-specific growth control and tumor-type specificity of oncogenes.
- Published
- 2006
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