Cutting-edge techniques developed by the Edinburgh Super-Resolution Imaging Consortium, based at Heriot-Watt University, have played a part in identifying properties in DNA's protective structure that could transform the way scientists think about the human genome.
The study, published in Cell, was funded by the Medical Research Council (MRC) and performed by scientists at the University of Edinburgh and Heriot-Watt University.
The bespoke microscope techniques developed to understand these very tiny structures are important not only for this project but for all of biology.
It showed that molecules involved in DNA's supportive scaffolding, once thought to be fixed, go through dynamic and responsive changes to shield against mutations, and this finding is expected to be crucial to understanding DNA damage and genome organisation. It could impact current thinking about DNA-linked diseases, including cancers.
In human cells, DNA is wrapped around proteins to form chromatin. Chromatin shields DNA from damage and regulates what genetic information can be read, a process known as transcription.
The study showed that a chemical called scaffold attachment factor A (SAF-A) binds to specific molecules known as caRNAs to form a protective chromatin mesh.
For the first time, this mesh was shown to be dynamic, assembling and disassembling and allowing the structure to be flexible and responsive to cell signals. In addition, loss of SAF-A was found to lead to abnormal folding of DNA and to promote damage to the genome.
Cutting-edge techniques used in the study were developed by the Edinburgh Super-Resolution Imaging Consortium, which is supported by the MRC, the Biotechnology and Biological Sciences Research Council and the Engineering and Physical Sciences Research Council.
Professor Rory Duncan, Head of the Institute for Biological Chemistry, Biophysics and Bioengineering at Heriot-Watt University, said, "The molecules involved in this study are as small to humans as Jupiter is large. The bespoke microscope techniques developed to understand these very tiny structures are important not only for this project but for all of biology.”
Nick Gilbert, Professor of Genetics at the University of Edinburgh's MRC Institute of Genetics and Molecular Medicine, said, “These findings are very exciting and have fundamental implications for how we understand our own DNA, showing that chromatin is the true guardian of the genome. The results open new possibilities for investigating how we might protect against DNA mutations that we see in diseases like cancer.”