Protein-binding microarray technology and ChIP-sequencing for the identification of novel targets of the human tumor suppressor AP2[alpha]

The mis-regulation of gene transcription in the living cell can be the cause of complex human diseases like cancer. One challenge of the post-genomic era of biomedical research is the development of in vitro techniques for the rapid and cost-effective analysis of regulatory transcriptional patterns of disease. Two crucial points for this endeavour have to be considered: (1) Sensitivity, since biologically active transcription factors are expressed at low amounts in the nucleus of the living cell and (2) the as close as feasible reconstitution of the nuclear microenvironment in order to guarantee as close to natural conditions for the performance of experiments as possible. The first part of this thesis reports on the application of protein-binding microarrays (PBM) bearing long-stranded DNA molecules for the analysis of a human disease-related protein, the human tumor suppressor activating enhancer-binding protein 2 alpha (AP2α). The second part of this thesis describes how chromatin-immunoprecipitation combined with high-throughput sequencing (ChIP-seq) and subsequent data analysis led to the discovery of a novel AP2α-binding motif in a cancer cell line model. We first developed a setup and protocol to perform on-chip protein-DNA molecule interaction analyses. Following this, recombinant AP2α protein was produced and purified using an E.coli host system. AP2α was subsequently assessed for its binding specificity to an array of ∼6000 human promoter and intergenic sequences. These experiments confirmed previously established AP2α DNA binding sequences and allowed the identification of novel ones. High and low binder sequences were selected from the PBM data and analyzed for specific AP2α binding in vivo utilizing reporter transfection and chromatin-immunoprecipitation (ChIP) assays. In contrast to the lowest AP2α-bound sequences, the highest PBM-bound sequences had significant effects on reporter gene expression. ChIP-qPCR revealed these sequences were bound by AP2α in vivo. From these results Kallikrein 5, a member of the kallikrein family of extracellular proteases that includes the prostate-specific antigen (PSA), which is currently emerging as one of the most prominent biomarkers of tumor progression for various types of cancers, and the growth-arrest specific 2 (GAS2) protein, which modulates cell susceptibility to p53-dependent apoptosis, were identified as novel AP2α targets. Finally, the binding patterns of AP2α from nuclear extracts of breast cancer tissue biopsies were assessed on the 6k human promoter arrays and compared to the binding patterns of 'healthy' tissue extracts. Overall these experiments confirmed known targets of AP2α. Interestingly a discrepancy of 26% was revealed when assessing the correlation of binding data from healthy and tumor tissue biopsies. This finding suggested that depending on the source of the protein, that is of either healthy or tumor tissue origin, the DNA-binding specificity of the protein factor under s