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PARIS: Some people carry a genetic variant is responsible for short telomeres - caps at the end of DNA that control ageing - and it could shave three or four years off their life, according to a new study.
It is the first time that a gene has been directly linked to the ageing process, scientists from Britain and The Netherlands reported in the journal Nature Genetics.
"What our study suggests is that some people are genetically programmed to age at a faster rate," said Tim Spector, a geneticist at King's College in the UK and co-leader of the research.
Gene makes you age faster
"The effect was quite considerable in those with the variant, equivalent to between three-to-four years of 'biological ageing'," he said.
The variant may make those people more vulnerable to age-related maladies, including heart disease and some types of cancer, the study concluded.
There are two different ways in which people grow old, recent research has shown.
Biological aging differs between people
Chronological ageing, the same for every one, is measured in years.
The pace of biological ageing, however, can vary from one person to the next, and occurs at the level of individual cells.
A critical component of biological ageing are tiny structures called telomeres, which sit like tiny protective caps on the tips of chromosomes.
Cell death triggered by teleomeres
Every time a cell divides, the telomeres get worn down.
Eventually, when the telomeres are worn beyond a certain point, cell death - part of the natural ageing process - is triggered.
Environmental factors such as smoking tobacco, exposure to toxins and unhealthy diet can also accelerate biological ageing.
"We found that those individuals carrying a particular genetic variant had shorter telomeres," explained Nilesh Samani, from University of Leicester in the UK and co-leader of the study.
Matching telomeres to genes
"Given the association of shorter telomeres with age-associated disease, the finding raises the question whether individuals carrying the variant are at greater risk of developing" age-linked diseases, he said.
Scientists scanned more than 500,000 genetic variations across the entire human genome hunting for matches in people who had short telomeres.
The culprit, it turned out, was a variant near a gene called TERC, which had previously been linked to accelerated ageing in mice.
Australian-American cell biologist Elizabeth Blackburn, who shared the Nobel Prize in Medicine last year for breakthrough research on telomeres, likened telomeres to "tips of shoelaces" - when you lose the little plastic end, the lace starts to fray.
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