Most human protein-coding genes are regulated by multiple, distinct promoters, suggesting that the choice of promoter is as important as its level of transcriptional activity. While the role of promoters as driver elements in cancer has been recognized, the contribution of alternative promoters to regulation of the cancer transcriptome remains largely unexplored. Here I will present how active promoters can be identified using RNA-Seq data, enabling the analysis of promoter activity in more than 18,000 samples. In order to study novel promoters, we generated long read RNA-Seq data in 10 different gastric cancer cell lines. Our results show that alternative promoters are frequently used, that they are predictive of patient survival, and that promoters are a major contribution to the diversity of isoforms in cancer.
Learning Objectives:
1. Learn about alternative promoters and their role in cancer
2. Learn how long read RNA-Seq helps to study the transcriptome