Konrad T. Howitz
Harvard University
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Publication
Featured researches published by Konrad T. Howitz.
Nature | 2003
Konrad T. Howitz; Kevin J. Bitterman; Haim Y. Cohen; Dudley W. Lamming; Siva Lavu; Jason G. Wood; Robert E. Zipkin; Phuong Chung; Anne Kisielewski; Li-Li Zhang; Brandy Scherer; David A. Sinclair
In diverse organisms, calorie restriction slows the pace of ageing and increases maximum lifespan. In the budding yeast Saccharomyces cerevisiae, calorie restriction extends lifespan by increasing the activity of Sir2 (ref. 1), a member of the conserved sirtuin family of NAD+-dependent protein deacetylases. Included in this family are SIR-2.1, a Caenorhabditis elegans enzyme that regulates lifespan, and SIRT1, a human deacetylase that promotes cell survival by negatively regulating the p53 tumour suppressor. Here we report the discovery of three classes of small molecules that activate sirtuins. We show that the potent activator resveratrol, a polyphenol found in red wine, lowers the Michaelis constant of SIRT1 for both the acetylated substrate and NAD+, and increases cell survival by stimulating SIRT1-dependent deacetylation of p53. In yeast, resveratrol mimics calorie restriction by stimulating Sir2, increasing DNA stability and extending lifespan by 70%. We discuss possible evolutionary origins of this phenomenon and suggest new lines of research into the therapeutic use of sirtuin activators.
Nature | 2004
Jason G. Wood; Blanka Rogina; Siva Lavu; Konrad T. Howitz; Stephen L. Helfand; Marc Tatar; David A. Sinclair
Caloric restriction extends lifespan in numerous species. In the budding yeast Saccharomyces cerevisiae this effect requires Sir2 (ref. 1), a member of the sirtuin family of NAD+-dependent deacetylases. Sirtuin activating compounds (STACs) can promote the survival of human cells and extend the replicative lifespan of yeast. Here we show that resveratrol and other STACs activate sirtuins from Caenorhabditis elegans and Drosophila melanogaster, and extend the lifespan of these animals without reducing fecundity. Lifespan extension is dependent on functional Sir2, and is not observed when nutrients are restricted. Together these data indicate that STACs slow metazoan ageing by mechanisms that may be related to caloric restriction.
Cell | 2008
Konrad T. Howitz; David A. Sinclair
Many plant molecules interact with and modulate key regulators of mammalian physiology in ways that are beneficial to health, but why? We propose that heterotrophs (animals and fungi) are able to sense chemical cues synthesized by plants and other autotrophs in response to stress. These cues provide advance warning about deteriorating environmental conditions, allowing the heterotrophs to prepare for adversity while conditions are still favorable.
Science | 2003
Rozalyn M. Anderson; Magda Latorre-Esteves; Ana Rute Neves; Siva Lavu; Oliver Medvedik; Christopher M. Taylor; Konrad T. Howitz; Helena Santos; David A. Sinclair
Calorie restriction (CR) slows aging in numerous species. In the yeast Saccharomyces cerevisiae, this effect requires Sir2, a conserved NAD+-dependent deacetylase. We report that CR reduces nuclear NAD+ levels in vivo. Moreover, the activity of Sir2 and its human homologue SIRT1 are not affected by physiological alterations in the NAD+:NADH ratio. These data implicate alternate mechanisms of Sir2 regulation by CR.
Science | 2004
Haim Y. Cohen; Christine M. Miller; Kevin J. Bitterman; Nathan R. Wall; Brian Hekking; Benedikt M. Kessler; Konrad T. Howitz; Myriam Gorospe; Rafael de Cabo; David A. Sinclair
Archive | 2004
David A. Sinclair; Konrad T. Howitz; Robert E. Zipkin; Kevin J. Bitterman; Dudley W. Lamming
Archive | 2006
David A. Sinclair; Li-Huei Tsai; Minh Nguyen; Konrad T. Howitz; Robert E. Zipkin; Kevin J. Bitterman
Archive | 2005
Konrad T. Howitz; Robert E. Zipkin
Archive | 2004
Kevin J. Bitterman; Konrad T. Howitz; David A. Sinclair; Robert E. Zipkin
Nature | 2004
Jason G. Wood; Blanka Rogina; Siva Lavu; Konrad T. Howitz; Stephen L. Helfand; Marc Tatar; David A. Sinclair