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Computational Modelling of Gene Regulation in Cancer: Coding the noncoding genome

  • Date: 3/14/2018 at 9:00 AM
  • Location: A1:111a, BMC, Husargatan 3
  • Doctoral student: Umer, Husen Muhammad
  • About the dissertation
  • Organiser: Beräkningsbiologi och bioinformatik
  • Contact person: Umer, Husen Muhammad
  • Disputation

In this thesis software programs to systematically investigate the process of gene regulation in the human genome were developed.

Technological advancements have enabled quantification of processes within and around us. The information stored within our body converts into petabytes of data. Processing and learning from such data requires comprehensive computational programs and software systems. We developed software programs to systematically investigate the process of gene regulation in the human genome. Gene regulation is a complex process where several genomic elements control expression of a gene through recruiting many transcription factor (TF) proteins. The TFs recognize specific DNA sequences known as motifs. DNA mutations in regulatory elements and particularly in TF motifs may cause gene deregulation. Therefore, defining the landscape of regulatory elements and their roles in cancer and complex diseases is of major importance.

We developed an algorithm (tfNet) to identify regulatory elements based on transcription factor binding sites. tfNet identified nearly 144,000 regulatory elements in five human cell lines. Investigating the elements we identified TF interaction networks and enrichment of many GWAS SNPs. We also defined the regulatory landscape for other conditions and species. Next, we investigated the role of regulatory elements in cancer. Cancer is initiated and developed by genetic aberrations in the genome. Genetic changes that are present in a cancer genome are obtained through whole genome sequencing technologies. We analyzed somatic mutations that had been detected in 326 whole genomes of liver cancer patients. Our results indicated 907 candidate mutations affecting TF motifs. Genome wide alignment of the mutated motifs revealed a significant enrichment of mutations in a highly conserved position of the CTCF motif. Gene expression analysis exhibited disruption of topologically associated domains in the mutated samples. We also confirmed the mutational pattern in pancreatic, gastric and esophagus cancers. Finally, enrichment of cancer associated gene sets and pathways suggested great role of noncoding mutations in cancer.

To systematically analyze DNA mutations in TF motifs, we developed an online database system (funMotifs). Publicly available datasets were collected for thousands experiments. The datasets were integrated using a logistic regression model. Functionality annotations and scores for motifs of 519 TFs were derived. The database allows for identification of variants affecting functional motifs in a selected tissue type. Finally, a comprehensive analysis was performed to identify mutations overlapping functional TF motifs in 37 cancer types. Somatic mutations from a pan-cancer cohort of 2,515 cancer whole genomes were investigated. A significant enrichment of mutations in the CpG site of the CEBPB motif was identified. Overall, 10,806 mutated regulatory elements were identified including 406 highly recurrent ones. Genes associated to the mutated elements were highly enriched for cancer-related pathways. Our analyses provide further insights onto the role of regulatory elements and their impacts on cancer development.