The genome's new clothes
30 October 2009
A major breakthrough study, published in Nature, has provided a complete roadmap of the human epigenome and has major implications for the treatment of human diseases and development of stem-cell based regenerative medicine. An epigenome may be thought of as the clothes that dress a genome, controlling the way genes are packaged and expressed without actually altering the underlying DNA code.
Epigenomes are flexible and can be changed by environmental factors such as diet, stress and chemical exposure, leading to changes in gene expression. These changes can be temporary or they can be more permanent, with some studies suggesting they can be passed down from generation to generation.
Such epigenetic changes have been shown to account for clear physical differences between otherwise genetically identical organisms.
Epigenetic changes are essential because correct timing of gene expression is needed for healthy physical development and for the prevention of genetically based diseases such as cancer.
Conducted by an international consortium, including three researchers linked to the University of Western Australia (UWA), this is the first study to fully sequence the human epigenome at single-base resolution, and required re-sequencing the human genome more than 30 times to map the location of tens of millions of tiny biological markers, known as cytosine methylation sites.
The paper also reveals a remarkable difference between normal human cells and stem cells in the type and pattern of methylation sites. The stem cells contain many methylations at unusual sites in the genome that must be actively propagated from one cell division to another. This finding could provide the key to understanding how stem cells can make many different cell types, while other human cells have defined roles that cannot be changed.
The lead researcher in this groundbreaking study was Dr Ryan Lister, a former UWA plant scientist now based at the Salk Institute for Biological Studies in San Diego, California. UWA PhD student Julian Tonti-Filippini, supervised by UWA Professor Harvey Millar, collaborated with Dr Lister to develop software tools for data handling, analysis and visualisation.
This is the second collaboration between the three scientists, following a successful study that mapped the complete epigenome of the model plant Arabidopsis thaliana, published last year in the journal Cell.
"This study represents a remarkable advance for human biology and medical science," Professor Millar said. "It has been a truly international collaborative effort and we are very excited about the ground breaking possibilities that may occur as a result.
"Julian originally designed his software to better understand gene expression in plants but with some further development, it evolved into a set of tools for digitalising the human epigenetic code."
Epigenetics
Defining the sequence of the human genome was hoped by many to be the end of the puzzle of defining what humans are and to be an answer to curing diseases. But some years on it is clear many other factors can affect our genes and how they perform – such as environment, diet and exercise – through what is called 'epigenetics'.
Related Articles:
- Whole genome study reveals clues to solving the mystery behind Kawasaki disease
- Our genome changes over lifetime
- Human genome research project discusses latest findings at medical law conference 2008
- First whole genome scan for links to Obsessive Compulsive Disorder reveals evidence for genetic susceptibility
Article Comments
Rate this article
Current Sponsors

Current Sponsors
|
Please be aware that we do not give advice on your individual medical condition, Information on this site must be discussed with your treating doctor. Virtual Medical Centre © 2002 - 2009 | Privacy Policy Last updated 21 Nov 2009 |
||
| ^ Back to Top | ||





