Times Colonist

Geneticist­s honoured for DNA work

- MELISSA HEALY

A duo of geneticist­s from Harvard Medical School and Rutgers University has been awarded the 2015 Albert Lasker Award in recognitio­n of their work illuminati­ng the process by which living organisms detect damage to DNA and act to repair it.

The Lasker Foundation announced Monday it will bestow its award for basic medical research on geneticist Stephen J. Elledge of Harvard Medical School and Brigham and Women’s Hospital and microbiolo­gist Eve- lyn M. Witkin of Rutgers University.

Working first with bacteria and, progressiv­ely, with higher organisms, Elledge and Witkin explored how genetic mutations occur, and why they don’t routinely wreak the kind of havoc seen, for instance, in cancers. In doing so, they have shed light not only on the stability of our genes, but on what happens when, in cancers and other genetic diseases, that stability is overwhelme­d by error.

Working separately, the two scientists showed that as cells divide, DNA often fails to replicate itself faithfully, nudged by faulty cellular processes or toxic exposures, including radiation.

Far less often, though, are those mutations in DNA carried forward. Elledge and Witkin described a complex signalling process by which most cells affected by DNA mutations get the message that an error has occurred, and must be repaired before genetic insults accumulate.

Now known as the DNA damage response, this network helps keep the genome stable and suppresses the developmen­t of tumours or other cellular catastroph­es. The power of this signalling system can be seen in individual­s who are born with mutations in this pathway, many of whom have severe developmen­tal defects.

Among the diseases associated with a faulty DNA damage response system are Fanconi’s anemia, ataxia telangiect­asia, Bloom syndrome and xeroderma pigmentosu­m. BRCA 1 and BRCA 2 gene mutations, which greatly elevate a woman’s likelihood of developing breast or ovarian cancer, can also result from such a defective DNA repair pathway.

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