In Bowel Cancer Study, ICR Scientists Use New Technique (Capture Hi-C) to Demonstrate Long-Range Cancer Risk Effects of DNA Looping and Single Nucleotide Variants in Gene Deserts

Single-letter genetic variations within parts of the genome once dismissed as “junk DNA” can increase cancer risk through wormhole-like effects on far-off genes, new research shows. Researchers have found that DNA sequences within “gene deserts,” so called because they are completely devoid of genes, can regulate gene activity elsewhere by forming DNA loops across relatively large distances. The study, led by scientists at The Institute of Cancer Research (ICR) (, London, helps solve a mystery about how genetic variations in parts of the genome that don't appear to be doing very much can increase cancer risk. Researchers developed a new technique to study the looping interactions and discovered that single-letter DNA variations linked to the development of bowel cancer were found in regions of the genome involved in DNA looping. Their study, published online on February 19, 2015, in Nature Communications, is the first to look comprehensively at these DNA interactions specifically in bowel cancer cells, and has implications for the study of other complex genetic diseases. The effort was funded by the EU, Cancer Research UK, Leukaemia & Lymphoma Research, and the ICR. The researchers developed a technique called Capture Hi-C to investigate long-range physical interactions between stretches of DNA. This allowed them to look at how specific areas of chromosomes interact physically in more detail than ever before. Previous techniques used to investigate long-range DNA interactions were not sensitive enough to produce definitive results. The researchers assessed 14 regions of DNA that contain single-letter variations previously linked to bowel cancer risk. They detected significant long-range interactions for all 14 regions, confirming their role in gene regulation.
Login Or Register To Read Full Story