This follows evidence that these structures shrink in length over an individual's lifetime and that this may contribute to several diseases including those commonly associated with ageing and, perhaps most importantly, the development of cancer.

Now the study is trying to understand how this process is controlled.

Jonathan Williams, from the Department of Genetics, is conducting postgraduate research into this field. He said: "DNA in human cells is arranged into 46 linear structures known as chromosomes. The ends of these molecules are particularly prone to damage from the environment inside the cell, and thus have special structures to protect them, termed telomeres.

"Telomeres consist of repeating pieces of DNA that vary in length between individuals. Important research over a number of years has shown that these structures shrink in length over an individual's lifetime and that this may contribute to several diseases.

Telomere shortening can be reversed in two specific ways:

• a protein termed telomerase can directly add new DNA to the end of telomeres.
• The second method is much less understood but most likely involves the copying of information from one telomere to another.

Said Mr Williams: "One of these methods must be activated during cancer development. The mechanisms controlling telomere length and the pathways reversing shortening largely remain a mystery.

"Now we are studying the ways in which changes to the chemical structure of DNA itself may control the lengthening of telomeres.

"Although these studies remain in their early stages it is hoped that the results may provide a better understanding of how the maintenance of telomeres is controlled, perhaps allowing for more targeted therapies for telomere associated disease in the future. "

Note: If no author is given, the source is cited instead.

• Genes
• Human Biology
• Forensics

• Biochemistry Research
• Biotechnology
• Genetics

• Telomere
• Senescence
• DNA repair
• Chromosomal crossover
• Dolly the Sheep
• Cloning