Construct · 1 fields · 4 citations
One name. One construct. A landmark on the map.
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The geneticist Hermann J. Muller coined the term telomere in 1938, from the Greek telos (end) and meros (part), to name the specialised structure that seals the natural end of a chromosome and keeps it from fusing with broken chromosome ends, and Barbara McClintock's parallel maize work in 1941 showed that chromosomes lacking such ends were unstable and cycled through breakage and fusion. A telomere is the region of repetitive DNA and its bound proteins that caps each chromosome tip: in humans it is thousands of copies of the short sequence TTAGGG held by a protein complex that hides the end from the cell's DNA-damage repair machinery. Elizabeth Blackburn and Joseph Gall first read out this repeated end sequence in the pond organism Tetrahymena in 1978, and in 1985 Carol Greider and Blackburn identified telomerase, the enzyme that rebuilds telomeric repeats and offsets the small loss of end sequence that ordinary DNA copying leaves behind each division. What marks the telomere as a landmark is that one physical structure ties together several processes at once: chromosome stability, the finite number of times most human cells divide, and the enzymatic maintenance that stem cells, germ cells, and many cancers rely on to keep dividing.[1][2][3][4]
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