If you are unfamiliar with the componentry of your genes, telomeres are the tiny caps on the ends of DNA strands. They shorten and fray as a cell ages, although the process is not strictly chronological. Obesity, illness and other conditions can accelerate the shortening, causing cells to age prematurely, while some evidence suggests that healthy lifestyles may preserve telomere length, delaying cell aging.
Nobel prize for chromosome find
Chromosomes house genetic material
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This year's Nobel prize for medicine goes to three US-based researchers who discovered how the body protects the chromosomes housing vital genetic code.
Elizabeth Blackburn, Carol Greider and Jack Szostak jointly share the award. Their work revealed how the chromosomes can be copied and has helped further our understanding on human ageing, cancer and stem cells.
The answer lies at the ends of the chromosomes - the telomeres - and in an enzyme that forms them - telomerase.
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FROM THE PM PROGRAMME
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The 46 chromosomes contain our genome written in the code of life - DNA.
When a cell is about to divide, the DNA molecules, housed on two strands, are copied.
But scientists had been baffled by an anomaly.
For one of the two DNA strands, a problem exists in that the very end of the strand cannot be copied.
Protecting the code of life
Therefore, the chromosomes should be shortened every time a cell divides - but in fact that is not usually the case.
If the telomeres did repeatedly shorten, cells would rapidly age.
|  The discoveries ... have added a new dimension to our understanding of the cell, shed light on disease mechanisms, and stimulated the development of potential new therapies 
The Nobel Assembly
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Conversely, if the telomere length is maintained, the cell would have eternal life, which could also be problematic. This happens in the case of cancer cells.
This year's prize winners solved the conundrum when they discovered how the telomere functions and found the enzyme that copies it.
Elizabeth Blackburn, of the University of California, San Francisco, and Jack Szostak, of Harvard Medical School, discovered that a unique DNA sequence in the telomeres protects the chromosomes from degradation.
Joined by Johns Hopkins University's Carol Greider, then a graduate student, Blackburn started to investigate how the teleomeres themselves were made and the pair went on to discover telomerase - the enzyme that enables DNA polymerases to copy the entire length of the chromosome without missing the very end portion.
Their research has led others to hunt for new ways to cure cancer.
It is hoped that cancer might be treated by eradicating telomerase. Several studies are under way in this area, including clinical trials evaluating vaccines directed against cells with elevated telomerase activity.
Some inherited diseases are now known to be caused by telomerase defects, including certain forms of anaemia in which there is insufficient cell divisions in the stem cells of the bone marrow.
The Nobel Assembly at Sweden's Karolinska Institute, which awarded the prize, said: "The discoveries... have added a new dimension to our understanding of the cell, shed light on disease mechanisms, and stimulated the development of potential new therapies."
Carol Greider, now 48, said she was phoned in the early hours with the news that she had won.
She said: "It's really very thrilling, it's something you can't expect."
Elizabeth Blackburn, now 60, shared her excitement, saying: "Prizes are always a nice thing. It doesn't change the research per se, of course, but it's lovely to have the recognition and share it with Carol Greider and Jack Szostak."
Professor Roger Reddel of the Children's Medical Research Institute in Sydney, Australia, said: "The telomerase story is an outstanding illustration of the value of basic research."
Sir Leszek Borysiewicz, chief executive of the Medical Research Council, said: "The Medical Research Council extends its congratulations to Blackburn, Greider and Szostak on winning the 2009 Nobel Prize.
"Their research on chromosomes helped lay the foundations of future work on cancer, stem cells and even human ageing, research areas that continue to be of huge importance to the scientists MRC funds and to the many people who will ultimately benefit from the discoveries they make."
telomere
Line breaks: telo|mere
Pronunciation: /ˈtiːlə(ʊ)mɪə
, ˈtɛl-/
NOUN
GeneticsOrigin
1940s: from Greek telos 'end' + meros 'part'.
Derivatives
chromosome
Line breaks: chromo|some 染色體
Pronunciation: /ˈkrəʊməsəʊm
/
NOUN
Biology
Each chromosome consists of a DNA double helix bearing a linear sequence of genes, coiled and recoiled around aggregated proteins (histones). Their number varies from species to species: humans have 22 pairs plus the two sex chromosomes (two X chromosomes in females, one X and one Y in males). During cell division each DNA strand is duplicated, and the chromosomes condense to become visible as distinct pairs of chromatids joined at the centromere
Each chromosome consists of a DNA double helix bearing a linear sequence of genes, coiled and recoiled around aggregated proteins (histones). Their number varies from species to species: humans have 22 pairs plus the two sex chromosomes (two X chromosomes in females, one X and one Y in males). During cell division each DNA strand is duplicated, and the chromosomes condense to become visible as distinct pairs of chromatids joined at the centromere
Origin
late 19th century: coined in German from Greek khrōma'colour' + sōma 'body'.
late 19th century: coined in German from Greek khrōma'colour' + sōma 'body'.
age
Syllabification: (age)
Pronunciation: /āj/
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