An important discovery in telomere biology has been made by a team of Australian scientists, with implications for conditions ranging from cancer to ageing and heart disease.
Telomeres are DNA segments at the ends of every human chromosome. As we age, telomere length naturally decreases.
Over the course of a lifetime, telomere shortening instructs ageing cells to stop dividing. This normally functions as a critical barrier to stop cancer.
However, some people are born with abnormally short telomeres and suffer from bone marrow failure, pulmonary fibrosis and high rates of cancer. Telomere length is also an important marker of disease risk for conditions such as cancer, heart disease and diabetes.
Telomere shortening causes chromosomes ends to resemble broken DNA. However, it has remained a mystery why telomeres change from healthy to unhealthy with age.
This research has identified the underlying cause.
“We knew that telomeres regulate cellular ageing, but our new data explain the trigger that makes telomeres unhealthy. Telomeres normally form a loop structure, where the chromosome end is hidden. We found that when the telomere loop unfolds, the chromosome end is exposed and the cell perceives this as broken DNA. It is not telomere length that matters, but telomere structure. The telomere loop becomes harder to form as telomeres get short,”
said Dr. Tony Cesare. The research project was led by Dr. Cesare, Head of the Genome Integrity Unit at Children’s Medical Research Institute (CMRI) at Westmead, in collaboration with scientists from CMRI as well as UNSW Sydney’s Katharina Gaus.
Additionally, the team identified that telomeres can also change structure in response to some chemotherapeutic agents, which helps kill cancer cells.
The results of this study have also proven how important technological advances are in the field of research. Dr. Cesare first developed his theories about telomere loops in 2002 when studying for his Ph.D. However, the technology was not available at the time to easily visualise telomere loops using microscopy.
However, the advent of super-resolution microscopy, which was awarded the 2014 Nobel Prize in Chemistry, made it possible to see telomere loops with a microscope. To complete this research, the team used super-resolution microscopes at four Sydney research institutions, and purchased the first Airyscan super-resolution microscope in Australia.
“This technology allowed us to see 10 times more detail than we had in the past. We could pass the physical limits of light and see the telomere loop structure,”
Dr. Cesare said. To complete the project, the team combined this breakthrough technology with powerful genetic models that mimic cellular aging.
“We were only the second group in the world to see telomere loops with super-resolution microscopes and the first to determine their function. It took us four and a half years to complete the project. It has been an enormous effort that I didn’t think was feasible five years ago. We’ve shown that it’s not just telomere length, but telomere structure and telomere health that we need to understand. The next step is to ask, can we correlate human health with telomere health? Our work suggests there is more to the story than just measuring telomere length,”
David Van Ly, Ronnie Ren Jie Low, Sonja Frölich, Tara K. Bartolec, Georgia R. Kafer, Hilda A. Pickett, Katharina Gaus, Anthony J. Cesare
Telomere Loop Dynamics in Chromosome End Protection
Molecular Cell (2018). DOI: 10.1101/279877