Surviving Longer

 

Twenty First Annual Darwin College Lecture Series 2006

CONFLICT

Lecture 7   :   3 March

Cynthia Kenyon

University of California, San Francisco

 

Abstract

Aging has long been assumed to be a passive consequence of molecular wear and tear, counteracted by the force of natural selection. But it's not so simple. Our discoveries have led to the realization that the aging process, like everything else in biology, is under exquisite regulation, in this case, by a complex, multifaceted hormonal system that affects aging in many species, including mammals. In 1993, we showed that changing a single gene in the small roundworm C. elegans can double its lifespan. This gene encodes an insulin/IGF-1 like receptor, which indicates that aging is regulated hormonally. By manipulating genes and cells, we have now been able to extend the lifespan and period of youthfulness of C. elegans by six times. We have found that signals from the reproductive system and sensory neurons influence lifespan. These signals act, at least in part, to control inslin/IGF-1 hormone signaling. These hormones influence the lifespan of the animal by coordinating the expression of a wide variety of subordinate genes, including antioxidant, stress response, antimicrobial, and novel genes, whose activities act in a cumulative fashion to determine the lifespan of the animal. Some of these subordinate genes can also influence the rate of onset of age-related disease. In this way, this hormone system couples the natural aging process to age-related disease susceptibility.

Biography

Cynthia Kenyon graduated valedictorian in chemistry and biochemistry from the University of Georgia in 1976. She received her PhD from MIT in 1981, where, in Graham Walker's laboratory, she was the first to look for genes on the basis of their activity profiles, discovering that DNA damaging agents activate a battery of DNA repair genes in E. coli. She then did postdoctoral studies with Nobel laureate Sydney Brenner at the MRC Laboratory of Molecular Biology in Cambridge, UK, studying the development of C. elegans. Since 1986 she has been at the University of California, San Francisco, where she was the Herbert Boyer Distinguished Professor of Biochemistry and Biophysics and is now an American Cancer Society Professor. Her early work led to the discovery that Hox genes, which were known to pattern the body segments Drosophila, also patterned the body of C. elegans. These findings demonstrated that Hox genes were not simply involved in segmentation, as thought, but instead were part of a much more ancient and fundamental metazoan patterning system. In 1993, Dr. Kenyon's discovery that a single-gene mutation could double the lifespan of C. elegans sparked an intensive study of the molecular biology of aging. Dr. Kenyon's findings have now led to the discovery that an evolutionarily-coserved hormone signaling system controls aging in other organisms as well, including mammals. Kenyon has received many honors, including the King Faisal Prize for Medicine, the American Association of Medical Colleges Award for Distinguished Research, the Ilse & Helmut Wachter Award for Exceptional Scientific Achievement, and La Fondation IPSEN Prize, for her findings. She is a member of the US National Academy of Sciences, the American Academy of Arts and Sciences, and the Institute of Medicine. She is now the director of the Hillblom Center for the Biology of Aging at UCSF. 


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