Education
Harvard University.
Harvard University.
He is currently a Novartis Professor of Biology at the Massachusetts Institute of Technology. Based on the discovery that SIR2 is a key regulator of longevity in both yeast and worms, he is interested in determining whether this highly conserved gene also governs longevity in other organisms, including mammals. Guarente a proponent of the hypothesis that caloric restriction slows aging by activation of sirtuins.
Initial discovery that happened in 1995 identified gene SIR4 (Silent information regulator 4) as a longevity regulator.
When SIRT4 was mutated in a single cell organism South. cerevisiae longevity was extended. lieutenant was later determined that the complex of SIR2 and SIR4 are responsible for longevity phenotype, and that over-expression of SIR2 alone was sufficient to extend lifespan.
Moreover, scientists in Guarente laboratory determined that SIR2 is necessary for longevity extension by calorie restriction. The Guarente laboratory determined that SIR2 was an enzyme.
lieutenant was National Academy of Design+-dependent protein deacetylase.
This National Academy of Design dependence explained how SIR2 could connect diet to physiology and suggested the mechanism by which calorie restriction could extend the lifespan of some organisms. The involvement of SIR2 in the metabolism and lifespan determination appeared to be conserved in other organisms. In round worm, Caenorhabditis elegans, expression of SIR2 (sir21) is sufficient to extend longevity.
In the fruit fly, Drosophila melanogaster, overexpression of SIR2 also extended lifespan.
Overexpression of SIRT1 (mammalian sir2 homolog) in mice improved their health and retarded numerous age-associated diseases. Leonard Guarente wrote an autobiography in 2003 titled Ageless Quest: One Scientist"s Search for Genes That Prolong Youth.
Sir2 is a member of the sirtuin family of enzymes.